CN1872857A - Reverse-turn mimetics and method relating thereto - Google Patents
Reverse-turn mimetics and method relating thereto Download PDFInfo
- Publication number
- CN1872857A CN1872857A CN 200610093787 CN200610093787A CN1872857A CN 1872857 A CN1872857 A CN 1872857A CN 200610093787 CN200610093787 CN 200610093787 CN 200610093787 A CN200610093787 A CN 200610093787A CN 1872857 A CN1872857 A CN 1872857A
- Authority
- CN
- China
- Prior art keywords
- benzyl
- alkyl
- amino
- methyl
- och
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Images
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Conformationally constrained compounds which mimic the secondary structure of reverse-turn regions of biologically active peptides and proteins are disclosed. Such reverse-turn mimetic structures have utility over a wide range of fields, including use as diagnostic and therapeutic agents. Libraries containing the reverse-turn mimetic structures of this invention are also disclosed as well as methods for screening the same to identify biologically active members. The invention also relates to the use of such compounds for inhibiting or treating disorders modulated by Wnt-signaling pathway, such as cancer, especially colorectal cancer, restenosis associated with angioplasty, polycystic kidney disease, aberrant angiogenesis disease, rheumatoid arthritis disease,or ulcerative colitis.
Description
The application is the dividing an application that be on October 11st, 2002, denomination of invention the applying date for the Chinese invention patent application 02822567.8 of " reverse turn mimetics and relevant method thereof ".
Technical field
The present invention generally relates to inflection (reverse-turn) model configuration and relevant chemical library thereof.The invention still further relates to the application in Cancerous disease treatment and comprise their pharmaceutical composition.
Background technology
The random screening molecule exists for many years as the possible activity of therapeutical agent, and causes many important drug discoveries.Though the development of molecular biology and calculational chemistry has caused increasing being called the interest of " rational drug design ", proved this technology and be not so good as the such quick or reliable of initial prediction.Therefore, drug screening has at random taken place to upgrade and turn back in interest in recent years.For this purpose, based on the exploitation in combinatorial chemistry library with this library is sought obtained concrete progress aspect biological activity member's the new technology of screening.
In general, the combinatorial chemistry library only is a kind of collection of molecule.This library with the chemical classes in the storehouse and the method that is used to produce library member and evaluation and the useful interactional member of biological target body change.Though still be at an early stage of development in this field, the method that produces and screen the library has become quite various and complicated.For example, one piece of nearest summary about various combination chemistry library has been determined multiple such technology (Dolle, J.Com.Chem., 2 (3): 383-433,2000), comprise applying marking and cold library member (Janda, Proc.Natl.Acad.Sci.USA 91:10779-10785,1994).
At first, the combinatorial chemistry library is generally limited to the member in peptide or Nucleotide source.For this purpose, people's such as Houghten technology illustration be called " two definition iteration " method be used for by division synthetic technology assembling solubility combined peptide library (Nature (London) 354:84-86,1991; Biotechniques 13:412-421,1992; Bioorg.Med.Chem.Lett.3:405-412,1993).By this technology, obtained to contain tens million of members' soluble peptide library.Shown that this library identifies the OPIOIDS peptide effectively; as methionine(Met)-and leucine enkephalin (Dooley and Houghten; Life Sci.52; 1509-1517; 1993); and N-acylations peptide library has been used to identify as the effective ethanoyl enkephalin of OPIOIDS antagonist (people such as Dooley; Proc.Natl.Acad.Sci.USA 90:10811-10815; 1993. more recently; made up full D-amino acids opioid peptides library; and it is carried out screening (people such as Dooley, Science 266:2019-2022,1994) at the analgesic activity of mu (" μ ") Opioid Receptors.
Have significant values though contain the member's who derives from peptide and Nucleotide combinatorial library, still need to contain the member's of different sources library in this area.For example, traditional peptide library only changes aminoacid sequence to a great extent and produces the library member.Though generally acknowledge that the secondary structure of peptide is important for biological activity, this peptide library is not given its restricted secondary structure of library member.
For this purpose, some investigator has attempted with disulfide linkage cyclisation peptide with secondary structure that restriction is provided more (people such as Tumelty, J.Chem.Soc.1067-68,1994; People such as Eichler, Peptide Res.7:300-306,1994).But generally speaking this cyclisation peptide still quite has flexibility, and bioavailability is poor, thereby the success that obtains is limited.
More recently, developed the non-peptide compound of more closely simulating the inflection secondary structure of finding in biological activity protein or the peptide.For example, the United States Patent (USP) 5,440,013 of Kahn and disclosed PCT WO94/03494, PCT WO01/00210A1 and the PCTWO01/16135A2 of Kahn, these documents disclose the non-peptide compound of the conformation restriction of simulation inflection three-dimensional structure.
Though, still need the small molecules of the secondary structure of simulating peptide in this area having obtained significant progress aspect the synthetic and evaluation of the reverse turn mimetics of conformation restriction.Also need to contain this member's library in this area, and be used for synthetic and screening technology, with the active library member of identification of organism at the library member of interested target body, particularly biological target body.For example the United States Patent (USP) 5,929,237 of Kahn and part thereof continue United States Patent (USP) 6,013, the compound that 458 conformations that also disclose the secondary structure in simulation biologically active peptides and proteinic inflection district limit.Obrecht has fully summarized synthetic and evaluation and their application (Advances in Med.Chem., 4,1-68,1999) in disease of the reverse turn mimetics of conformation restriction.
The present invention also satisfies these requirements, and provides further relevant advantage by the compound that the conformation that the simulation biologically active peptides and the secondary structure in proteinic inflection district are provided limits.
The Wnt signal pathway is regulated multiple different process, comprises that (people such as Moon, 1997, Trends Genet.13,157-162 take place and grow for cell growth, tumour; People such as Miller, 1999, Oncogene 18,7860-7872; Nusse and Varmus, 1992, Cell 69,1073-1087; Cadigan and Nusse, 1997, Genes Dev.11,3286-3305; Peifer and Polais, 2000 Science 287,1606-1609; Polakis 2000, Genes Dev.14,1837-1851).The Wnt signal pathway has been done abundant research in multiple different organism.The activation of transcribing of having found the white mediation of TCF4/ beta-catenin that the Wnt signal transduction causes in its biological function, play an important role (people such as Molenaar, 1996, Cell 86, people such as 391-399:Gat, 1998 Cell 95,605-614; People such as Orford, 1999J.Cell.Biol.146,855-868).
Under the situation that does not have the Wnt signal, tumor suppressor gene adenomatoid polyp and colorectal carcinoma gene (the APC) (people such as Su that interacts in vain with serine kinase glycogen synthase kinase (GSK)-3 β and beta-catenin simultaneously, 1993, Science 262,1734-1737; People such as Yost, 1996 GenesDev.10,1443-1454; People such as Hayashi, 1997, Proc.Natl.Acad.Sci.USA, 94,242-247; People such as Sakanaka, 1998, Proc.Natl.Acad.Sci.USA, 95,3020-3023; Sakanaka and William, 1999, J.Biol.Chem 274,14090-14093).The phosphorylation of the APC that GSK-3 β causes is regulated APC and the white interaction of beta-catenin, thereby can regulate the white semiotic function of beta-catenin (people such as B.Rubinfeld, Science 272,1023,1996).It is white that beta-catenin is stablized in the effect of Wnt signal, makes it transfer to nuclear, there the member of the lymphocyte enhanser factor (LEF1)/T-cytokine (TCF4) family of it and transcription factor interact (people such as Behrens, 1996Nature 382,638-642; People such as Hsu, 1998, Mol.Cell.Biol.18, people such as 4807-4818:Roose, 1999Science 285,1923-1926).
Shown recently a kind of known oncogene c-myc be beta-catenin white/target gene of transcribing of TCF4 mediation (people such as He, 1998 Science, 281 1509-1512; People such as Kolligs, 1999 Mol.Cell.Biol.19,5696-5706).Many other important function of gene comprise also participating in tumorigenic cyclin D1 and metalloprotease, have determined to be subjected to the TCF4/ beta-catenin to transcribe the adjusting of approach (people such as Crawford, 1999, Oncogene18,2883-2891 in vain; People such as Shtutman, 1999, Proc.Natl.Acad.Sci.USA., 11,5522-5527; Tetsu and McCormick, 1999 Nature, 398,422-426).
And the overexpression of having found several downstream media of Wnt signal effect is regulated apoptosis (people such as Moris, 1996, Proc.Natl.Acad.Sci.USA, 93,7950-7954; People such as He, 1999, Cell 99,335-345; People such as Orford, 1999J.Cell.Biol., 146,855-868; Strovel and Sussman, 1999, Exp.Cell.Res., 253,637-648).The apoptosis-induced s of the overexpression of APC in the human colorectal cancer cell (people such as Moris, 1996, Proc.Natl.Acad.Sci.USA., 93,7950-7954), the white ectopic expression of beta-catenin suppresses the relevant apoptosis of the forfeiture of adsorbing with extracellular matrix (people such as Orford, 1999, J.Cell Biol.146,855-868).The cell survival of the inhibition blocking-up Wnt-1-mediation that the TCF4/ beta-catenin that the dominant negative mutant expression of TCF4 causes is transcribed in vain, and make cell have susceptibility (people such as Shaoqiong Chen, 2001, J.Cell Biol. to apoptotic stimulus thing such as anticarcinogen, 152,1,87-96), and APC sudden change suppresses apoptosis (people such as Tao Zhang by allowing constitutive character survivin to express (a kind of known inhibitor of apoptosis protein matter), 2001, Cancer Research, 62,8664-8667).
Though do not find the sudden change of Wnt gene in people's cancer, APC that takes place in most colorectum tumour or the white sudden change of beta-catenin cause activating inadequately TCF4, overexpression c-myc and produce tumor growth (people such as Bubinfeld, 1997, Science, 275,1790-1792; People such as Morin, 1997, Science, 275,1787-1790; People such as Casa, 1999, Cell.Growth.Differ.10,369-376).In colorectal carcinoma 85% and multiple other the cancer tumor suppressor gene (APC) lose or inactivation (Kinzler and Vogelstein, 1996, Cell 87,159-170), the main effect of APC is the effect of the negative conditioning agent of Wnt signal transduction cascade.The core feature of this approach relates to by interacting with the macrocomplex based on Axin that comprises APC regulates the stable and location in the white kytoplasm storehouse of beta-catenin.This interaction causes the white phosphorylation of beta-catenin, thereby aims at it to degrade.
In the protein interaction test, identified CREB conjugated protein (CBP)/p300 at first, at first by with (the people such as Chrivia that combines of transcription factor CREB, 1993, Nature, 365,855-859), interaction by itself and adenovirus transforming protein E1A afterwards (people such as Stein, 1990, J.Viol., 64,4421-4427; People such as Eckner, 1994, Genes.Dev., 8,869-884).CBP has the potential that participates in the various kinds of cell function and comprise the transcriptional coactivator function (people such as Shikama, 1997, Trends.Cell.Biol., 7,230-236; Janknecht and Hunter, 1996, Nature, 383,22-23).CBP/p300 strengthen the siamois promotor (a kind of known Wnt target body) of the white mediation of beta-catenin activation (people such as Hecht, 2000, EMBO J.19,8,1839-1850).Beta-catenin directly combines the territory with the CREB of CBP in vain and interacts, and beta-catenin is white and CBP is collaborative to stimulate white transcription activating (Ken-Ichi Takemaru and Randall T.Moon, 2000J.Cell.Biol., 149 of TCF4/ beta-catenin, 2,249-254).
According to this background knowledge, the white and CBP complex body of the TCF4/ beta-catenin of Wnt approach can be considered to regulate the target molecule of cell growth, tumour generation and apoptosis etc.That is to say, thus need by suppress CBP block the TCF4/ beta-catenin in vain the approach of transcribing can be used for the treatment of the particularly compound of colorectal carcinoma of cancer.
Brief description of drawings
Fig. 1 shows about the IC of compound of the present invention for the SW480 cell
50The figure that measures wherein measures cell growth inhibition to the SW480 cell to obtain IC under the situation of the compound of the embodiment of different concns 4 preparations
50Value.Particularly, measure the inhibition degree of this test compound to Lampyridea and renilla luciferase activity.Found that the IC of the anti-SW480 cell growth of this test compound
50Open as table 4.Detailed method is identical with embodiment 6 disclosed methods.
Summary of the invention
The present invention relates to simulate the compound (also being called " reverse turn mimetics " and relevant chemical library thereof here) of the conformation restriction of the biological peptide and the secondary structure in protein inflection district.The present invention also openly comprises library and synthetic and the screening method of this compound.
Inflection model configuration of the present invention can be used as biologically active agent, includes, but is not limited to as diagnosis, prevents and/or treats agent.Inflection model configuration of the present invention library can be used for identifying this biologically active agent.In implementation process of the present invention, described library can comprise tens of to hundreds of independent inflection structures (also being called " member ") to thousands of (or more) here.
Compound of the present invention has following general formula (I):
Wherein A is-(CHR
3)-or-(C=O)-, B is-(CHR
4)-or-(C=O)-, D is-(CHR
5)-or-(C=O)-, E is-(ZR
6-or-(C=O)-, G is-(XR
7)
n-,-(CHR
7)-(NR
8)-,-(C=O)-(XR
9)-or-(C=O)-, W is-Y (C=O)-,-(C=O) NH-,-(SO
2)-or do not exist, Y is oxygen or sulphur, X and Z are nitrogen or CH independently, n=0 or 1; And R
1, R
2, R
3, R
4, R
5, R
6, R
7, R
8And R
9Identical or different and be independently selected from resistates, connector and the solid carrier of amino acid side chain moiety or derivatives thereof, described molecule and their steric isomer.
A therein is-(CHR
3)-, B is-(C=O)-, D is-(CHR
5)-, E is-(C=O)-, and G is-(XR
7)
n-embodiment in, compound of the present invention has following formula (II):
Wherein W, Y and n such as above definition, and R
1, R
2, R
3, R
5And R
7As definition in the following detailed description.
A therein is-(C=O)-, B is-(CHRR
4)-, D is-(C=O)-, E is-(ZR
6)-, and G is-(C=O)-(XR
9)-embodiment in, compound of the present invention has following formula (III):
Wherein W, Y and n such as above definition, Z is nitrogen or CH (if Z is CH, then X is a nitrogen), and R
1, R
2, R
4, R
6And R
9Definition as described in detail below.
A therein is-(C=O)-, B is-(CHR
4)-, D is-(C=O)-, E is-(ZR
6)-, and G is (XR
7)
n-embodiment in, compound of the present invention has following general formula (IV):
Wherein W, Y and n such as above definition, Z be nitrogen or CH (if Z is a nitrogen, then n is 0, and if Z is CH, then X be nitrogen and n is not 0), and R
1, R
2, R
4, R
6And R
7As definition in the following detailed description.
The invention still further relates to the library that comprises with the compound of following formula (I), and be used for the method in synthetic this library and be used to screen the method for described library with the identification of organism active compound.Also disclose and comprised compound of the present invention and pharmaceutically acceptable carrier or the combined composition of thinner.
Particularly, the present invention relates to comprise the pharmaceutical composition of these compounds, be used for the treatment of the disease that comprise cancer relevant with the Wnt signal pathway.The invention still further relates to the method that is used for the treatment of the disease that comprise cancer relevant with the Wnt signal pathway.
To be more clearly visible these and other aspect of the present invention with reference to accompanying drawing and following detailed description description.For this purpose, quote from various bibliographys here, they describe some method, compound and/or composition in more detail, and are all quoted as a reference.
Below with illustration the present invention in more detail.
In one aspect of the invention, the inflection model configuration with following formula (I) is disclosed:
Wherein A is-(CHR
3)-or-(C=O)-, B is-(CHR
4)-or-(C=O)-, D is-(CHR
5)-or-(C=O)-, E is-(ZR
6)-or-(C=O)-, G is-(XR
7)
n-,-(CHR
7)-(NR
8)-,-(C=O)-(XR
9)-or-(C=O)-, W is-Y (C=O)-,-(C=O) NH-,-(SO
2)-or do not exist, Y is oxygen or sulphur, X and Z are nitrogen or CH independently, n=0 or 1; And R
1, R
2, R
3, R
4, R
5, R
6, R
7, R
8And R
9Identical or different and be independently selected from resistates, connector and the solid carrier of amino acid side chain moiety or derivatives thereof, described molecule and their steric isomer.
More particularly, R
1, R
2, R
3, R
4, R
5, R
6, R
7, R
8And R
9Be independently selected from: amino C
2-5Alkyl, guanidine C
2-5Alkyl, C
1-4Alkyl guanidine radicals C
2-5Alkyl, two C
1-4Alkyl guanidine radicals-C
2-5Alkyl, amidino groups C
2-5Alkyl, C
1-4Alkyl amidine C
2-5Alkyl, two C
1-4Alkyl amidine C
2-5Alkyl, C
1-3(wherein said substituting group is independently selected from one or more amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to the phenyl of alkoxyl group, phenyl, replacement
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3Alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or hydroxyl), (wherein the substituting group on the benzyl is independently selected from one or more amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C for the benzyl of benzyl, replacement
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-3Alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or hydroxyl), (wherein said substituting group is independently selected from one or more amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C for the naphthyl of naphthyl, replacement
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3Alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or hydroxyl), (wherein said substituting group is independently selected from one or more amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C for two phenyl methyls of two phenyl methyl, replacement
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3Alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or hydroxyl), (wherein said substituting group is independently selected from one or more amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C for the pyridyl of pyridyl, replacement
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3Alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or hydroxyl), pyridyl C
1-4The pyridyl C of alkyl, replacement
1-4(wherein said pyridine substituting group is independently selected from one or more amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to alkyl
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3Alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or hydroxyl), pyrimidyl C
1-4The pyrimidyl C of alkyl, replacement
1-4(wherein said pyrimidine substituting group is independently selected from one or more amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to alkyl
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3Alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or hydroxyl), triazine-2-base-C
1-4The triazine of alkyl, replacement-2-base-C
1-4(wherein said triazine substituting group is independently selected from one or more amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to alkyl
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3Alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or hydroxyl), imidazoles C
1-4The imidazoles C of alkyl, replacement
1-4(wherein said imidazole substituent is independently selected from one or more amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to alkyl
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3Alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or hydroxyl), imidazolinyl C
1-4Alkyl, N-amidino groups piperazinyl-N-C
0-4Alkyl, hydroxyl C
2-5Alkyl, C
1-5Alkylamino C
2-5Alkyl, hydroxyl C
2-5Alkyl, C
1-5Alkylamino C
2-5Alkyl, C
1-5Dialkyl amido C
2-5Alkyl,
N-amidinopiperidinyl C
1-4The amino cyclohexyl C of alkyl and 4-
0-2Alkyl.
In one embodiment, R
1, R
2, E R
6R with G
7, R
8, R
9Identical or different, and the resistates of representation compound, and the R of A
3, B R
4Or the R of D
5Be selected from the amino acid side chain moiety or derivatives thereof.Terminology used here " resistates of compound " means at R
1, R
2, R
5, R
6, R
7, R
8And/or R
9Any part, reagent, compound, carrier, molecule, connector, amino acid, peptide or protein that position and inflection model configuration are covalently bound.This term also comprises amino acid side chain moiety and derivative thereof.
Any amino acid side chain moiety that terminology used here " amino acid side chain moiety " representative exists in naturally occurring protein includes, but is not limited to the naturally occurring amino acid side chain moiety that table 1 is determined.Other naturally occurring amino acid side chain moiety of the present invention includes, but is not limited to 3, the pendant moiety of 5-Dibromotyrosine, iodogorgoic acid, oxylysine, Gla, Tyrosine O-phosphate and phosphoserine.In addition, the glycosylation amino acid side chain also can be used to implement the present invention, includes, but is not limited to glycosylation Threonine, Serine and l-asparagine.
Table 1
Except naturally occurring amino acid side chain moiety, amino acid side chain moiety of the present invention also comprises its multiple derivative." derivative " of used here amino acid side chain moiety comprises modification and/or the change to naturally occurring amino acid side chain moiety.For example, the amino acid side chain moiety of L-Ala, Xie Ansuan, leucine, Isoleucine and phenylalanine generally can classify as lower alkanols alkyl, aryl or arylalkyl part.The derivative of amino acid side chain moiety comprise other straight or branched, ring-type or acyclic, replacement or unsubstituted, saturated or undersaturated lower alkanols alkyl, aryl or arylalkyl part.
Here used " lower alkane base section " comprises 1-12 carbon atom, and " lower alkanols aryl moiety " comprises 6-12 carbon atom, and " lower alkanols aralkyl moiety " comprises 7-12 carbon atom.Therefore, in one embodiment, the amino acid side chain derivative is selected from C
1-12Alkyl, C
6-12Aryl and C
7-12Arylalkyl, and in a more preferred embodiment, be selected from C
1-7Alkyl, C
6-10Aryl and C
7-11Arylalkyl.
Amino acid side chain derivative of the present invention also comprises the derivative of the replacement of lower alkanols alkyl, aryl and arylalkyl part, wherein said substituting group be selected from (but being not limited to) one or more following chemical parts :-OH ,-OR ,-COOH ,-COOR ,-CONH
2,-NH
2,-NHR ,-NRR ,-SH ,-SR ,-SO
2R ,-SO
2H ,-SOR and halogen (comprising F, Cl, Br and I), the R under the wherein various situations be independently selected from straight or branched, ring-type or acyclic, replacement or unsubstituted, saturated or undersaturated lower alkanols alkyl, aryl or aralkyl part.And, ring-type lower alkanols alkyl of the present invention, aryl and arylalkyl partly comprise naphthalene, and heterogeneous ring compound such as thiophene, pyrroles, furans, imidazoles, azoles, thiazole, pyrazoles, 3-pyrroline, tetramethyleneimine, pyridine, pyrimidine, purine, quinoline, isoquinoline 99.9 and carbazole.The amino acid side chain derivative also comprises the assorted alkyl derivative of the moieties of lower alkanols alkyl and aralkyl moiety, includes, but is not limited to alkyl and alkyl aryl phosphine acid esters and silane.
Representational R
1, R
2, R
5, R
6, R
7, R
8And R
9Partly specifically include, but is not limited to-OH ,-OR ,-COR ,-COOR ,-CONH
2,-CONR ,-CONRR ,-NH
2,-NHR ,-NRR ,-SO
2R and-COSR, the R under the wherein various situations be as above definition.
In another embodiment, except as amino acid side chain moiety or derivatives thereof (or R
1, R
2, R
5, R
6, R
7, R
8And R
9The residuum of the compound under the situation) outside, R
1, R
2, R
5, R
6, R
7, R
8Or R
9Can be to be beneficial to the connector that compound is connected with another part or compound.For example, compound of the present invention can be connected with one or more compound known such as vitamin H, is used for diagnosis or screening analysis.And, R
1, R
2, R
5, R
6, R
7, R
8Or R
9Can be that compound is connected to connector on the solid carrier (as being used for solid-phase peptide synthetic carrier), perhaps selectively can be carrier itself.In this embodiment, with another part or compound or with being connected of solid carrier preferably at R
1, R
2, R
7Or R
8The position, and more preferably at R
1Or R
2The position.
A therein is-(CHR
3)-, B is-(C=O)-, D is-(CHR
5)-, E is-(C=O)-, G is-(XR
7)
n-embodiment in, inflection simulated compound of the present invention has following formula (II):
R wherein
1, R
2, R
3, R
5, R
7, W, X and n such as above definition.In a preferred embodiment, R
1, R
2And R
7The residuum of representation compound, and R
3Or R
5Be selected from amino acid side chain moiety.
A therein is-(C=O)-, B is-(CHR
4)-, D is-(C=O)-, E is-(ZR
6)-, G is-(C=O)-and (XR
9)-embodiment in, inflection simulated compound of the present invention has following formula (III):
R wherein
1, R
2, R
4, R
6, R
9, W and X such as above definition, Z is nitrogen or CH (if Z is CH, then X is a nitrogen).In a preferred embodiment, R
1, R
2, R
6And R
9The residuum of representation compound, and R
4Be selected from amino acid side chain moiety.A therein is-(C=O)-, B is-(CHR
4)-, D is-(C=O)-, E is-(ZR
6)-, G is (XR
7)
n-more particular embodiment in, inflection simulated compound of the present invention has following formula (IV):
R wherein
1, R
2, R
4, R
6, R
7, W, X and n such as above definition, Z be nitrogen or CH (if Z is a nitrogen then n is 0, if Z is CH then X be nitrogen and n is not 0).In a preferred embodiment, R
1, R
2, R
6And R
7The residuum of representation compound, and R
4Be selected from amino acid side chain moiety.In this case, if Z and X are respectively CH, R then
6Or R
7Can be selected from amino acid side chain moiety.
Inflection model configuration of the present invention can be by using suitable initial ingredient (hereinafter referred to as " building block ") preparation.In brief, in the inflection model configuration with formula (II) synthetic, the first and second building block couplings are formed the first-the second intermediate product of combination, if necessary, with the 3rd and/or the 4th building block coupling with the 3rd-Di four intermediate products of forming combination (if perhaps can be commercially available, can use single the 3rd intermediate product), the first-the second intermediate product that will make up then and the 3rd-Di four intermediate products (or the 3rd intermediate product) coupling obtain the first-the second-Di, three-Di, four intermediate products (or the first-the second-Di, three intermediate products), and this product cyclisation is obtained inflection model configuration of the present invention.Selectively, the inflection model configuration of formula (II) can prepare by substep ground in solution each independent building block of coupling successively or by solid phase synthesis commonly used in solid-phase peptide is synthetic each independent building block of coupling successively.
In the context of the present invention, " first building block " has following formula S1:
R wherein
2As above definition, and R is for being applicable to peptide synthetic protecting group.Suitable R group comprises alkyl, and in preferred embodiments, R is a methyl.These first building blocks can be easily by CH (OR)
2-CHO or CH (OR)
2-CH
2-Hal (wherein Hal means halogen atom) is by reduction amination or displacement H
2N-R
2Substitution reaction and synthesize.
" second building block " of the present invention has following formula S2:
L wherein
1Be activated carboxylic group such as halogen atom, R
4As above definition, and P is for being applicable to peptide synthetic amino protecting group.Preferred protecting group comprises t-butyldimethylsilyl (TBDMS), tert-butoxycarbonyl (BOC), methoxycarbonyl (MOC), 9H-fluorenyl methoxy carbonyl (FMOC) and allyloxy carbonyl (Alloc).If L is-C (O) NHR, then-NHR can be carboxyl-protecting group.The amino acid of N-protected can be commercially available.For example, FMOC amino acid can obtain from multiple source.These compounds to the conversion of second building block of the present invention can easily realize by the amino acid whose hydroxy-acid group activation with N-protected.Suitable activatory hydroxy-acid group comprises that X wherein is the acyl halide of halogenide such as muriate or bromide; X wherein is the acid anhydrides of acyl group such as ethanoyl; reactive ester such as N-hydroxy-succinamide ester and phenyl-pentafluoride base ester, and the active intermediate product of other activation intermediate product as in the coupled reaction of using carbodiimide such as dicyclohexyl carbodiimide (DCC), forming.
As under the situation of second building block, this compound can be prepared by people such as Zaloom (J.Org Chem.46:5173-76,1981) disclosed reaction by the amino acid of correspondence at amino acid whose azido-derivative.
Selectively, first parts of the present invention can have following formula S1 ':
Wherein R such as above definition, and L
2Be leavings group such as halogen atom or tosyl group, and second parts of the present invention can have following formula S2 ':
R wherein
2, R
3With P such as above definition.
" the 3rd building block " of the present invention has following formula S3a or S3b:
Wherein G, E, L
1And L
2As above definition.The 3rd suitable building block can be commercially available from multiple source, perhaps can be by any known organic chemistry method preparation.
More particularly, the inflection model configuration of the present invention of synthesis type (II) by the following method: the first-the second intermediate product that makes the reaction of first building block and second building block obtain making up, make the first-the second intermediate product of combination react the first-the second-Di, three-Di, four intermediate products that obtain making up with the 3rd building block successively then, then this intermediate product cyclisation is obtained the inflection model configuration.
Have structure I ' the general synthetic of inflection can synthesize by following technology.By using coupling reagent such as phosgene first building block 1 and 2 couplings of second building block to be obtained the first-the second intermediate product 1-2 behind the N-deprotection as following illustrative combination:
R wherein
1, R
2, R
4, R
7, Fmoc, Moc and X such as above definition, and Pol represents polymeric carrier.
Synthesizing of representational building block of the present invention as preparing described in embodiment and the work embodiment.
Formula (III) and inflection model configuration (IV) can make by being similar to above disclosed model components synthetic technology, but wherein building block are carried out suitable modification.
As above-mentioned, the reverse turn mimetics of people's such as Kahn USP 6,013,458 can be used as biologically active agent, for example diagnoses, prevention and therapeutical agent.At this USP 6,013, the opiate receptor-binding activity that has presented representative reverse turn mimetics among 458 the embodiment 9, the reverse turn mimetics of wherein finding this invention suppresses combining of radiolabeled enkephalin derivative and δ and μ opiate acceptor effectively, and data wherein show the application of these reverse turn mimetics as receptor stimulant and potential pain killer.
Inflection model configuration of the present invention will can be used as biologically active agent, for example diagnose, prevention and therapeutical agent.
Therefore, because compound according to the present invention has the inflection model configuration, it can be used for regulating warm-blooded animal cell signaling transcription factor related peptides, comprises the compound of using the formula (I) of significant quantity to this animal.
And inflection model configuration of the present invention can also be used for suppressing the warm-blooded animal peptide effectively and combine with the PTB territory; Be used for regulating warm-blooded animal G protein coupled receptor (GPCR) and ionic channel; Be used to regulate the cytokine of warm-blooded animal.
Simultaneously, the compound of discoverable type (I) particularly the compound of formula (VI) suppress effectively or treat the disease of regulating, for example cancer, particularly colorectal carcinoma by the Wnt signal pathway.
R wherein
aFor having the aryl bicyclic of 8-11 ring members, it can have 1-3 heteroatoms that is selected from nitrogen, oxygen or sulphur; R
bFor having the monocyclic aryl of 5-7 ring members, it can have 1-2 heteroatoms that is selected from nitrogen, oxygen or sulphur; And the aromatic ring in the compound can have one or more substituting groups that are selected from halogenide, hydroxyl, cyano group, low alkyl group and lower alkoxy.
Therefore, an object of the present invention is to provide a kind of compound with general formula (VI) of safety and significant quantity and pharmaceutical composition of pharmaceutically acceptable carrier of comprising, described composition can be used for the treatment of by the Wnt signal pathway particularly the TCF4-beta-catenin white-disease that the CBP complex body is regulated.
And, the invention provides a kind of method that suppresses growth of tumour cell by the composition that uses the invention described above; A kind of by the composition that uses the invention described above the method for inducing apoptosis of tumour cell; A kind of by the composition that uses the invention described above treat by the TCF4-beta-catenin white-method of the disease that the CBP complex body is regulated; Treat the method for cancer such as colorectal carcinoma with a kind of by using composition of the present invention and other anticarcinogen such as 5 FU 5 fluorouracil (5-FU), taxol, cis-platinum, ametycin, Tegafur, Raltitrexed, capecitabine and irinotecan etc.
In an embodiment preferred of the present invention, that compound of the present invention has is following (6S, 10R)-configuration:
R wherein
aAnd R
bHave the implication identical with above definition.
In another aspect of this invention, the library that comprises inflection model configuration of the present invention is disclosed.Library of the present invention is in case by assembly, individual member that then can the Screening and Identification biologically active.For example, this library screening to the biological activity member can comprise that the combination of for example estimating the library member is active or estimate the effect of library member to functional analysis.Screening is generally finished by library member's (or subclass of library member) is contacted with target body interested such as antibody, enzyme, acceptor or clone.Here can be called " biological activity library member " or " biological activity stand-in " with the interactional library member of target body interested.For example, the biological activity stand-in can be can with the library member of antibody or receptors bind, library member that can inhibitory enzyme, perhaps can cause or antagonism for example with the library member of clone function associated reaction.In other words, library screening of the present invention is determined which library member can interact with one or more interested biological target bodys.And, if interact, then can be from the library member the active stand-in of identification of organism.Identify that from the library biological activity stand-in of single (or limited quantity) obtain the inflection model configuration of biologically active own, thereby, and can also be further used for significantly promotion to the evaluation of lead compound in these fields as diagnosis, prevention or therapeutical agent.
The synthetic of the peptide mimics in library of the present invention can be united of the present invention first, second and finish with the 3rd building block by using known peptide synthetic technology.More particularly, any aminoacid sequence can be added to the N-end and/or the C-end of the reverse turn mimetics of conformation restriction.For this purpose, can go up by known technology (for example referring to John M.Stewart and Janis D.Young at solid carrier (as the PAM resin), Solid Phase PeptideSynthesis, 1984, Pierce Chemical Comp., Rockford, Ill), perhaps on the resin that silyl connects, add (referring to people such as Randolph, J Am Chem.Soc.117:5712-14,1995) and synthesize stand-in by alcohol.
In addition, the combination of solution and solid phase synthesis technique can be used for synthetic peptide mimics of the present invention.For example, solid carrier can be used for the synthesizing linear peptide sequence, add that of sequence until inflection the conformation restriction.The inflection model configuration that the conformation that before suits by solution synthetic technology synthetic can be limited is added to solid phase synthesis (reverse turn mimetics that promptly has the conformation restriction of N-end and C-end can be used as the next amino acid that remains to be added on the linear peptides) as next " amino acid " then.Behind reverse turn mimetics structure calling sequence, can then add other amino acid to finish and solid carrier bonded peptide with the conformation restriction.Selectively, the peptide sequence of the terminal protection of LINEAR N-end and C-can synthesize on solid carrier, removes the inflection model configuration coupling of using known solution coupling technology to limit with conformation in solution then from carrier.
In another aspect of this invention, the method that is used to make up described library is disclosed.Traditional combinatorial chemistry technique (for example referring to people such as Gallop, J.Med.Chem.37:1233-1251,1994) allows by continuously agent combination being prepared a large amount of compounds apace to basic molecular skeleton.Combination technique has been used for structure and has derived from naturally occurring amino acid whose peptide library.For example, by obtain 20 quilts suitable protection with different amino acid whose 20 kinds of mixtures, and make the coupling of one of each and 20 amino acid, set up 400 (promptly 20
2) library of dipeptides.Repeating this process causes for 7 times preparation to comprise about 26,000,000,000 (promptly 20
8) peptide library of individual octapeptide.
Particularly, the peptide mimics in library of the present invention synthetic can be used known peptide synthetic technology and be finished, for example the general route in following [4,4,0] reverse turn mimetics library:
The FlexChemReactor Block that the synthetic use of the peptide mimics in library of the present invention has 96 hole flat boards finishes by known technology.In above route, ' Pol ' represents a kind of bromoacetal resin (Advanced ChemTech), and the process such as the following illustration that describe in detail.
Step 1
With the bromoacetal resin (37mg, 0.98mmol/g) and the R in DMSO
2The solution of-amine (1.4mL) places the Robbins block (FlexChem) with 96 hole flat boards.Reaction mixture is used rotary oven [Robbins Scientific] vibration 12 hours down in 60 ℃.With DMF, MeOH washing resin, wash with DCM then.
Step 2
The solution of the Fmoc amino acid that is available commercially (4 equivalent), PyBob (4 equivalent), HOAt (4 equivalent) and DIEA (12 equivalent) that will be in DMF is added to resin.Reaction mixture, with DMF, MeOH washing resin, is being washed with DCM after 12 hours then in vibration under the room temperature.
Step 3
By being added in 25% piperidines among the DMF in the DMF swollen resin, and reaction mixture was vibrated under room temperature 30 minutes before the reaction.Repeat this deprotection steps once more, and, wash with DCM then with DMF, methanol wash resin.The solution of hydrazine acid (hydrazine acid) (4 equivalent), HOBt (4 equivalent) and DIC (4 equivalent) that will be in DMF is added to resin, and reaction mixture was vibrated under room temperature 12 hours.With DMF, MeOH washing resin, wash with DCM then.
Step 4a (wherein hydrazine acid is the MOC carbamate)
The plastic resin treatment that with formic acid (the every hole of 1.2mL) step 3 is obtained under the room temperature 18 hours.After removing by filter resin, use SpeedVac[SAVANT] concentrating under reduced pressure filtrate obtains product, is oil.With 50% water/dilution in acetonitrile product, then in freezing back freeze-drying.
Step 4b (wherein the acid of Fmoc hydrazine is used for preparing urea by isocyanic ester)
Before reaction, be added in 25% piperidines among the DMF, and reaction mixture was vibrated under room temperature 30 minutes by DMF swollen resin.Repeat this deprotection steps once more, and, wash with DCM then with DMF, methanol wash resin.Toward before reaction by being added in the isocyanic ester (5 equivalent) among the DCM in the DCM swollen resin.Under the room temperature reaction mixture vibration after 12 hours, with DMF, MeOH washing resin, is washed with DCM then.With formic acid (the every hole of 1.2mL) under room temperature with plastic resin treatment 18 hours.After removing by filter resin, use SpeedVac[SAVANT] concentrating under reduced pressure filtrate obtains product, is oil.With 50% water/dilution in acetonitrile product, then in freezing back freeze-drying.
Step 4c (wherein the acid of Fmoc-hydrazine is used for preparing urea by the active amino manthanoate)
By being added in 25% piperidines among the DMF in the DMF swollen resin, and reaction mixture was vibrated under room temperature 30 minutes before the reaction.Repeat this deprotection steps once more,, wash with DCM then with DMF, MeOH washing resin.Toward before reaction by being added in chloroformic acid p-nitrophenyl ester (5 equivalent) and the diisopropylethylamine (5 equivalent) among the DCM in the DCM swollen resin.Reaction mixture, with DMF, MeOH washing resin, is being washed with DCM after 12 hours then in vibration under the room temperature.Be added in the primary amine among the DCM in the resin, at room temperature kept 12 hours, and, wash with DCM then with DMF, MeOH washing resin.At room temperature use formic acid (the every hole of 1.2mL) with plastic resin treatment 18 hours after the reaction.After removing by filter resin, use SpeedVac[SAVANT] concentrating under reduced pressure filtrate obtains product, is oil.With 50% water/dilution in acetonitrile product, then in freezing back freeze-drying.
For producing these member libraries, according to the synthetic crucial intermediate product hydrazine acid of the illustrative method of preparation embodiment.
Table 2 has shown can [4,4,0] prepared in accordance with the present invention reverse turn mimetics library, and its representational preparation such as embodiment 4 provide.
Reverse turn mimetics library, [table 2] [4,4,0]
| Numbering | R 2 | R 4 | R 7 | R 1-Y’ | Molecular weight | M+H |
| 1 | 2，4-Cl 2-benzyl | The 4-HO-benzyl | Allyl group | OCH 3 | 533 | 534 |
| 2 | 2，4-Cl 2-benzyl | 4-NO 2-benzyl | Allyl group | OCH 3 | 562 | 563 |
| 3 | 2，4-Cl 2-benzyl | 2，4-F 2-benzyl | Allyl group | OCH 3 | 553 | 554 |
| 4 | 2，4-Cl 2-benzyl | The 4-Cl-benzyl | Allyl group | OCH 3 | 552 | 553 |
| 5 | 2，4-Cl 2-benzyl | 2, the two phenylethyls of 2- | Allyl group | OCH 3 | 594 | 595 |
| 6 | 2，4-Cl 2-benzyl | The 3-t-BU-4-HO-benzyl | Allyl group | OCH 3 | 590 | 591 |
| 7 | 2，4-Cl 2-benzyl | The 4-Me-benzyl | Allyl group | OCH 3 | 531 | 532 |
| 8 | 2，4-Cl 2-benzyl | Cyclohexyl methyl | Allyl group | OCH 3 | 523 | 524 |
| 9 | 2，4-Cl 2-benzyl | The 4-F-benzyl | Allyl group | OCH 3 | 535 | 536 |
| 10 | 2，4-Cl 2-benzyl | The 2-Cl-benzyl | Allyl group | OCH 3 | 552 | 553 |
| 11 | 2，4-Cl 2-benzyl | 2，4-Cl 2-benzyl | Allyl group | OCH 3 | 586 | 587 |
| 12 | 2，4-Cl 2-benzyl | Naphthalene-2-ylmethyl | Allyl group | OCH 3 | 567 | 568 |
| 13 | 2，4-Cl 2-benzyl | The 4-HO-benzyl | Benzyl | OCH 3 | 583 | 584 |
| 14 | 2，4-Cl 2-benzyl | 4-NO 2-benzyl | Benzyl | OCH 3 | 612 | 613 |
| 15 | 2，4-Cl 2-benzyl | 2，4-F 2-benzyl | Benzyl | OCH 3 | 603 | 604 |
| 16 | 2，4-Cl 2-benzyl | The 4-Cl-benzyl | Benzyl | OCH 3 | 602 | 603 |
| 17 | 2，4-Cl 2-benzyl | 2, the two styroyls of 2- | Benzyl | OCH 3 | 644 | 645 |
| 18 | 2，4-Cl 2-benzyl | The 3-t-Bu-4-HO-benzyl | Benzyl | OCH 3 | 640 | 641 |
| 19 | 2，4-Cl 2-benzyl | The 4-Me-benzyl | Benzyl | OCH 3 | 582 | 583 |
| 20 | 2，4-Cl 2-benzyl | Cyclohexyl methyl | Benzyl | OCH 3 | 574 | 575 |
| 21 | 2，4-Cl 2-benzyl | The 4-F-benzyl | Benzyl | OCH 3 | 585 | 586 |
| 22 | 2，4-Cl 2-benzyl | The 2-Cl-benzyl | Benzyl | OCH 3 | 602 | 603 |
| 23 | 2，4-Cl 2-benzyl | 2，4-Cl 2-benzyl | Benzyl | OCH 3 | 636 | 637 |
| 24 | 2，4-Cl 2-benzyl | Naphthalene-2-ylmethyl | Benzyl | OCH 3 | 618 | 619 |
| 25 | 2，4-Cl 2-benzyl | The 4-HO-benzyl | Allyl group | OCH 3 | 479 | 480 |
| 26 | 2，4-Cl 2-benzyl | 4-NO 2-benzyl | Allyl group | OCH 3 | 508 | 509 |
| 27 | 2，4-Cl 2-benzyl | 2，4-F 2-benzyl | Allyl group | OCH 3 | 499 | 500 |
| 28 | 2，4Cl 2-benzyl | The 4-Cl-benzyl | Allyl group | OCH 3 | 497 | 498 |
| 29 | Styroyl | 2,2 pairs of phenylethyls | Allyl group | OCH 3 | 539 | 540 |
| 30 | Styroyl | The 3-t-Bu-4-HO-benzyl | Allyl group | OCH 3 | 535 | 536 |
| 31 | Styroyl | The 4-Me-benzyl | Allyl group | OCH 3 | 477 | 478 |
| 32 | Styroyl | Cyclohexyl methyl | Allyl group | OCH 3 | 469 | 470 |
| 33 | Styroyl | The 4-F-benzyl | Allyl group | OCH 3 | 481 | 482 |
| 34 | Styroyl | The 2-Cl-benzyl | Allyl group | OCH 3 | 497 | 498 |
| 35 | Styroyl | 2，4-Cl 2-benzyl | Allyl group | OCH 3 | 531 | 532 |
| 36 | Styroyl | Naphthalene-2-ylmethyl | Allyl group | OCH 3 | 513 | 514 |
| 37 | Styroyl | The 4-HO-benzyl | Benzyl | OCH 3 | 529 | 530 |
| 38 | Styroyl | 4-NO 2-benzyl | Benzyl | OCH 3 | 558 | 559 |
| 39 | Styroyl | 2，4-F 2-benzyl | Benzyl | OCH 3 | 549 | 550 |
| 40 | Styroyl | The 4-Cl-benzyl | Benzyl | OCH 3 | 547 | 548 |
| 41 | Styroyl | 2, the two phenylethyls of 2- | Benzyl | OCH 3 | 589 | 590 |
| 42 | Styroyl | The 3-t-Bu-4-HO-benzyl | Benzyl | OCH 3 | 585 | 586 |
| 43 | Styroyl | The 4-Me-benzyl | Benzyl | OCH 3 | 527 | 528 |
| 44 | Styroyl | Cyclohexyl-methyl | Benzyl | OCH 3 | 519 | 520 |
| 45 | Styroyl | The 4-F-benzyl | Benzyl | OCH 3 | 531 | 532 |
| 46 | Styroyl | The 2-Cl-benzyl | Benzyl | OCH 3 | 547 | 548 |
| 47 | Styroyl | 2，4-Cl 2-benzyl | Benzyl | OCH 3 | 582 | 583 |
| 48 | Styroyl | Naphthalene-2-ylmethyl | Benzyl | OCH 3 | 563 | 564 |
| 49 | Styroyl | The 4-HO-benzyl | Allyl group | OCH 3 | 497 | 498 |
| 50 | Styroyl | 4-NO 2-benzyl | Allyl group | OCH 3 | 526 | 527 |
| 51 | Styroyl | 2，4-F 2-benzyl | Allyl group | OCH 3 | 517 | 518 |
| 52 | Styroyl | The 4-Cl-benzyl | Allyl group | OCH 3 | 515 | 516 |
| 53 | The 4-F-phenylethyl | 2, the two phenylethyls of 2- | Allyl group | OCH 3 | 557 | 558 |
| 54 | The 4-F-phenylethyl | The 3-t-BU-4-HO-benzyl | Allyl group | OCH 3 | 553 | 554 |
| 55 | The 4-F-phenylethyl | The 4-Me-benzyl | Allyl group | OCH 3 | 495 | 496 |
| 56 | The 4-F-phenylethyl | Cyclohexyl-methyl | Allyl group | OCH 3 | 487 | 488 |
| 57 | The 4-F-phenylethyl | The 4-F-benzyl | Allyl group | OCH 3 | 499 | 500 |
| 58 | The 4-F-phenylethyl | The 2-Cl-benzyl | Allyl group | OCH 3 | 515 | 516 |
| 59 | The 4-F-phenylethyl | 2，4-Cl 2-benzyl | Allyl group | OCH 3 | 549 | 550 |
| 60 | The 4-F-phenylethyl | Naphthalene-2-ylmethyl | Allyl group | OCH 3 | 531 | 532 |
| 61 | The 4-F-phenylethyl | The 4-HO-benzyl | Benzyl | OCH 3 | 547 | 548 |
| 62 | The 4-F-phenylethyl | 4-NO 2-benzyl | Benzyl | OCH 3 | 576 | 577 |
| 63 | The 4-F-phenylethyl | 2，4-F 2-benzyl | Benzyl | OCH 3 | 567 | 568 |
| 64 | The 4-F-phenylethyl | The 4-Cl-benzyl | Benzyl | OCH 3 | 565 | 566 |
| 65 | The 4-F-phenylethyl | 2, the two phenylethyls of 2- | Benzyl | OCH 3 | 607 | 608 |
| 66 | The 4-F-phenylethyl | The 3-t-BU-4-HO-benzyl | Benzyl | OCH 3 | 603 | 604 |
| 67 | The 4-F-phenylethyl | The 4-Me-benzyl | Benzyl | OCH 3 | 545 | 546 |
| 68 | The 4-F-phenylethyl | Cyclohexyl-methyl | Benzyl | OCH 3 | 537 | 538 |
| 69 | The 4-F-phenylethyl | The 4-F-benzyl | Benzyl | OCH 3 | 549 | 550 |
| 70 | The 4-F-phenylethyl | The 2-Cl-benzyl | Benzyl | OCH 3 | 565 | 566 |
| 71 | The 4-F-phenylethyl | 2，4-Cl 2-benzyl | Benzyl | OCH 3 | 599 | 600 |
| 72 | The 4-F-phenylethyl | Naphthalene-2-ylmethyl | Benzyl | OCH 3 | 581 | 582 |
| 73 | The 4-F-phenylethyl | The 4-HO-benzyl | Allyl group | OCH 3 | 509 | 510 |
| 74 | The 4-F-phenylethyl | 4-NO 2-benzyl | Allyl group | OCH 3 | 538 | 539 |
| 75 | The 4-F-phenylethyl | 2，4-F 2-benzyl | Allyl group | OCH 3 | 529 | 530 |
| 76 | The 4-F-phenylethyl | The 4-Cl-benzyl | Allyl group | OCH 3 | 527 | 528 |
| 77 | The 4-MeO-phenylethyl | 2, the two phenylethyls of 2- | Allyl group | OCH 3 | 569 | 570 |
| 78 | The 4-MeO-phenylethyl | The 3-t-Bu-4-HO-benzyl | Allyl group | OCH 3 | 565 | 566 |
| 79 | The 4-MeO-phenylethyl | The 4-Me-benzyl | Allyl group | OCH 3 | 507 | 508 |
| 80 | The 4-MeO-phenylethyl | Cyclohexyl-methyl | Allyl group | OCH 3 | 499 | 500 |
| 81 | The 4-MeO-phenylethyl | The 4-F-benzyl | Allyl group | OCH 3 | 511 | 512 |
| 82 | The 4-MeO-phenylethyl | The 2-Cl-benzyl | Allyl group | OCH 3 | 527 | 528 |
| 83 | The 4-MeO-phenylethyl | 2，4-Cl 2-benzyl | Allyl group | OCH 3 | 561 | 562 |
| 84 | The 4-MeO-phenylethyl | Naphthalene-2-ylmethyl | Allyl group | OCH 3 | 543 | 544 |
| 85 | The 4-MeO-phenylethyl | The 4-HO-benzyl | Benzyl | OCH 3 | 559 | 560 |
| 86 | The 4-MeO-phenylethyl | 4-NO 2-benzyl | Benzyl | OCH 3 | 588 | 589 |
| 87 | The 4-MeO-phenylethyl | 2，4-F 2-benzyl | Benzyl | OCH 3 | 579 | 580 |
| 88 | The 4-MeO-phenylethyl | The 4-Cl-benzyl | Benzyl | OCH 3 | 577 | 578 |
| 89 | The 4-MeO-phenylethyl | 2, the two phenylethyls of 2- | Benzyl | OCH 3 | 619 | 620 |
| 90 | The 4-MeO-phenylethyl | The 3-t-Bu-4-HO-benzyl | Benzyl | OCH 3 | 615 | 616 |
| 91 | The 4-MeO-phenylethyl | The 4-Me-benzyl | Benzyl | OCH 3 | 557 | 558 |
| 92 | The 4-MeO-phenylethyl | Cyclohexyl methyl | Benzyl | OCH 3 | 549 | 550 |
| 93 | The 4-MeO-phenylethyl | The 4-F-benzyl | Benzyl | OCH 3 | 561 | 562 |
| 94 | The 4-MeO-phenylethyl | The 2-Cl-benzyl | Benzyl | OCH 3 | 577 | 578 |
| 95 | The 4-MeO-phenylethyl | 2，4-Cl 2-benzyl | Benzyl | OCH 3 | 612 | 613 |
| 96 | The 4-MeO-phenylethyl | Naphthalene-2-ylmethyl | Benzyl | OCH 3 | 593 | 594 |
| 97 | Isopentyl | The 4-HO-benzyl | The styryl methyl | OCH 3 | 521 | 522 |
| 98 | Isopentyl | 4-NO 2-benzyl | The styryl methyl | OCH 3 | 550 | 551 |
| 99 | Isopentyl | 2，4-F 2-benzyl | The styryl methyl | OCH 3 | 541 | 542 |
| 100 | Isopentyl | The 4-Cl-benzyl | The styryl methyl | OCH 3 | 539 | 540 |
| 101 | Isopentyl | 2, the two phenylethyls of 2- | The styryl methyl | OCH 3 | 581 | 582 |
| 102 | Isopentyl | The 3-t-Bu-4-HO-benzyl | The styryl methyl | OCH 3 | 497 | 498 |
| 103 | Isopentyl | The 4-Me-benzyl | The styryl methyl | OCH 3 | 519 | 520 |
| 104 | Isopentyl | Cyclohexyl methyl | The styryl methyl | OCH 3 | 511 | 512 |
| 105 | Isopentyl | The 4-F-benzyl | The styryl methyl | OCH 3 | 523 | 524 |
| 106 | Isopentyl | The 2-Cl-benzyl | The styryl methyl | OCH 3 | 539 | 540 |
| 107 | Isopentyl | 2，4-Cl 2-benzyl | The styryl methyl | OCH 3 | 574 | 575 |
| 108 | Isopentyl | Naphthalene-2-ylmethyl | The styryl methyl | OCH 3 | 555 | 556 |
| 109 | Isopentyl | The 4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 563 | 564 |
| 110 | Isopentyl | 4-NO 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 592 | 593 |
| 111 | Isopentyl | 2，4-F 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 583 | 584 |
| 112 | Isopentyl | The 4-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 582 | 583 |
| 113 | Isopentyl | 2, the two phenylethyls of 2- | 2，6-Cl 2-benzyl | OCH 3 | 624 | 625 |
| 114 | Isopentyl | The 3-t-Bu-4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 540 | 541 |
| 115 | Isopentyl | The 4-Me-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 562 | 563 |
| 116 | Isopentyl | Cyclohexyl methyl | 2，6-Cl 2-benzyl | OCH 3 | 554 | 555 |
| 17 | Isopentyl | The 4-F-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 565 | 566 |
| 118 | Isopentyl | The 2-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 582 | 583 |
| 119 | Isopentyl | 2，4-Cl 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 616 | 617 |
| 120 | Isopentyl | Naphthalene-2-ylmethyl | 2，6-Cl 2-benzyl | OCH 3 | 598 | 599 |
| 121 | The 3-MeO-propyl group | The 4-HO-benzyl | The styryl methyl | OCH 3 | 523 | 524 |
| 122 | The 3-MeO-propyl group | 4-NO 2-benzyl | The styryl methyl | OCH 3 | 552 | 553 |
| 123 | The 3-MeO-propyl group | 2，4-F 2-benzyl | The styryl methyl | OCH 3 | 543 | 544 |
| 124 | The 3-MeO-propyl group | The 4-Cl-benzyl | The styryl methyl | OCH 3 | 541 | 542 |
| 125 | The 3-MeO-propyl group | 2, the two phenylethyls of 2- | The styryl methyl | OCH 3 | 583 | 584 |
| 126 | The 3-MeO-propyl group | The 3-t-Bu-4-HO-benzyl | The styryl methyl | OCH 3 | 499 | 500 |
| 127 | The 3-MeO-propyl group | The 4-Me-benzyl | The styryl methyl | OCH 3 | 521 | 522 |
| 128 | The 3-MeO-propyl group | Cyclohexyl-methyl | The styryl methyl | OCH 3 | 513 | 514 |
| 129 | The 3-MeO-propyl group | The 4-F-benzyl | The styryl methyl | OCH 3 | 525 | 526 |
| 130 | The 3-MeO-propyl group | The 2-Cl-benzyl | The styryl methyl | OCH 3 | 541 | 542 |
| 131 | The 3-MeO-propyl group | 2，4-Cl 2-benzyl | The styryl methyl | OCH 3 | 575 | 576 |
| 132 | The 3-MeO-propyl group | Naphthalene-2-ylmethyl | The styryl methyl | OCH 3 | 557 | 558 |
| 133 | The 3-MeO-propyl group | The 4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 565 | 566 |
| 134 | The 3-MeO-propyl group | 4-NO 2Benzyl | 2，6-Cl 2-benzyl | OCH 3 | 594 | 595 |
| 135 | The 3-MeO-propyl group | 2，4-F 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 585 | 586 |
| 136 | The 3-MeO-propyl group | The 4-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 584 | 585 |
| 137 | The 3-MeO-propyl group | 2, the two phenylethyls of 2- | 2，6-Cl 2-benzyl | OCH 3 | 626 | 627 |
| 138 | The 3-MeO-propyl group | The 3-t-Bu-4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 541 | 542 |
| 139 | The 3-MeO-propyl group | The 4-Me-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 563 | 564 |
| 140 | The 3-MeO-propyl group | Cyclohexyl-methyl | 2，6-Cl 2-benzyl | OCH 3 | 556 | 557 |
| 141 | The 3-MeO-propyl group | The 4-F-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 567 | 568 |
| 142 | The 3-MeO-propyl group | The 2-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 584 | 585 |
| 143 | The 3-MeO-propyl group | 2，4-Cl 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 618 | 619 |
| 144 | The 3-MeO-propyl group | Naphthalene-2-ylmethyl | 2，6-Cl 2-benzyl | OCH 3 | 600 | 601 |
| 145 | The 4-MeO-phenylethyl | The 4-HO-benzyl | The styryl methyl | OCH 3 | 585 | 586 |
| 146 | The 4-MeO-phenylethyl | 4-NO 2-benzyl | The styryl methyl | OCH 3 | 614 | 615 |
| 147 | The 4-MeO-phenylethyl | 2，4-F 2-benzyl | The styryl methyl | OCH 3 | 605 | 606 |
| 148 | The 4-MeO-phenylethyl | The 4-Cl-benzyl | The styryl methyl | OCH 3 | 603 | 604 |
| 149 | The 4-MeO-phenylethyl | 2, the two phenylethyls of 2- | The styryl methyl | OCH 3 | 645 | 646 |
| 150 | The 4-MeO-phenylethyl | The 3-t-Bu-4-HO-benzyl | The styryl methyl | OCH 3 | 561 | 562 |
| 151 | The 4-MeO-phenylethyl | The 4-Me-benzyl | The styryl methyl | OCH 3 | 583 | 584 |
| 152 | The 4-MeO-phenylethyl | Cyclohexyl-methyl | The styryl methyl | OCH 3 | 575 | 576 |
| 153 | The 4-MeO-phenylethyl | The 4-F-benzyl | The styryl methyl | OCH 3 | 587 | 588 |
| 154 | The 4-MeO-phenylethyl | The 2-Cl-benzyl | The styryl methyl | OCH 3 | 603 | 604 |
| 155 | The 4-MeO-phenylethyl | 2，4-Cl 2-benzyl | The styryl methyl | OCH 3 | 638 | 639 |
| 156 | The 4-MeO-phenylethyl | Naphthalene-2-ylmethyl | The styryl methyl | OCH 3 | 619 | 620 |
| 157 | The 4-MeO-phenylethyl | The 4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 628 | 629 |
| 158 | The 4-MeO-phenylethyl | 4-NO 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 657 | 658 |
| 159 | 4-MeO-benzyl ethyl | 2, the 4-F-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 648 | 649 |
| 160 | The 4-MeO-phenylethyl | The 4-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 646 | 647 |
| 161 | The 4-MeO-phenylethyl | 2, the two phenylethyls of 2- | 2，6-Cl 2-benzyl | OCH 3 | 688 | 689 |
| 162 | The 4-MeO-phenylethyl | The 3-t-Bu-4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 604 | 605 |
| 163 | The 4-MeO-phenylethyl | The 4-Me-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 626 | 627 |
| 164 | The 4-MeO-phenylethyl | Cyclohexyl methyl | 2，6-Cl 2-benzyl | OCH 3 | 618 | 619 |
| 165 | The 4-MeO-phenylethyl | The 4-F-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 630 | 631 |
| 166 | The 4-MeO-phenylethyl | The 2-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 646 | 647 |
| 167 | The 4-MeO-phenylethyl | 2，4-Cl 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 680 | 681 |
| 168 | The 4-MeO-phenylethyl | Naphthalene-2-ylmethyl | 2，6-Cl 2-benzyl | OCH 3 | 662 | 663 |
| 169 | Tetrahydrofuran (THF)-2-ylmethyl | The 4-HO-benzyl | The styryl methyl | OCH 3 | 535 | 536 |
| 170 | Tetrahydrofuran (THF)-2-ylmethyl | 4-NO 2-benzyl | The styryl methyl | OCH 3 | 564 | 565 |
| 171 | Tetrahydrofuran (THF)-2-ylmethyl | 2，4F 2-benzyl | The styryl methyl | OCH 3 | 555 | 556 |
| 172 | Tetrahydrofuran (THF)-2-ylmethyl | The 4-Cl-benzyl | The styryl methyl | OCH 3 | 553 | 554 |
| 173 | Tetrahydrofuran (THF)-2-ylmethyl | 2, the two phenylethyls of 2- | The styryl methyl | OCH 3 | 595 | 596 |
| 174 | Tetrahydrofuran (THF)-2-ylmethyl | The 3-t-Bu-4-HO-benzyl | The styryl methyl | OCH 3 | 511 | 512 |
| 175 | Tetrahydrofuran (THF)-2-ylmethyl | The 4-Me-benzyl | The styryl methyl | OCH 3 | 533 | 534 |
| 176 | Tetrahydrofuran (THF)-2-ylmethyl | Cyclohexyl-methyl | The styryl methyl | OCH 3 | 525 | 526 |
| 177 | Tetrahydrofuran (THF)-2-ylmethyl | The 4-F-benzyl | The styryl methyl | OCH 3 | 537 | 538 |
| 178 | Tetrahydrofuran (THF)-2-ylmethyl | The 2-Cl-benzyl | The styryl methyl | OCH 3 | 553 | 554 |
| 179 | Tetrahydrofuran (THF)-2-ylmethyl | 2，4-Cl 2-benzyl | The styryl methyl | OCH 3 | 588 | 589 |
| 180 | Tetrahydrofuran (THF)-2-ylmethyl | Naphthalene-2-ylmethyl | The styryl methyl | OCH 3 | 569 | 570 |
| 181 | Tetrahydrofuran (THF)-2-ylmethyl | The 4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 577 | 578 |
| 182 | Tetrahydrofuran (THF)-2-ylmethyl | 4-NO 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 606 | 607 |
| 183 | Tetrahydrofuran (THF)-2-ylmethyl | 2，4-F 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 597 | 598 |
| 184 | Tetrahydrofuran (THF)-2-ylmethyl | The 4-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 596 | 597 |
| 185 | Tetrahydrofuran (THF)-2-ylmethyl | 2, the two phenylethyls of 2- | 2，6-Cl 2-benzyl | OCH 3 | 638 | 639 |
| 186 | Tetrahydrofuran (THF)-2-ylmethyl | The 3-t-Bu-4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 553 | 554 |
| 187 | Tetrahydrofuran (THF)-2-ylmethyl | The 4-Me-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 575 | 576 |
| 188 | Tetrahydrofuran (THF)-2-ylmethyl | Cyclohexyl-methyl | 2，6-Cl 2-benzyl | OCH 3 | 568 | 569 |
| 189 | Tetrahydrofuran (THF)-2-ylmethyl | The 4-F-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 579 | 580 |
| 190 | Tetrahydrofuran (THF)-2-ylmethyl | The 2-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 596 | 597 |
| 191 | Tetrahydrofuran (THF)-2-ylmethyl | 2，4-Cl 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 630 | 631 |
| 192 | Tetrahydrofuran (THF)-2-ylmethyl | Naphthalene-2-ylmethyl | 2，6-Cl 2-benzyl | OCH 3 | 612 | 613 |
| 193 | Styroyl | The 4-HO-benzyl | Methyl | (4-Me-phenyl) amino | 528 | 529 |
| 194 | Styroyl | The 4-HO-benzyl | Methyl | (4-Cl-phenyl) amino | 548 | 549 |
| 195 | Styroyl | The 4-HO-benzyl | Methyl | Phenyl amino | 514 | 515 |
| 196 | Styroyl | The 4-HO-benzyl | Methyl | ((R)-α-Jia Jibianji) amino | 542 | 543 |
| 197 | Styroyl | The 4-HO-benzyl | Methyl | Benzylamino | 528 | 529 |
| 198 | Styroyl | The 4-HO-benzyl | Methyl | (4-MeO-phenyl) amino | 544 | 545 |
| 199 | Styroyl | The 4-HO-benzyl | Methyl | (4-Br-phenyl) amino | 592 | 593 |
| 200 | Styroyl | The 4-HO-benzyl | Methyl | (4-CF 3-phenyl) amino | 582 | 583 |
| 201 | Styroyl | The 4-HO-benzyl | Methyl | Amyl group amino | 508 | 509 |
| 202 | Styroyl | The 4-HO-benzyl | Methyl | (2-phenylethyl) amino | 542 | 543 |
| 203 | Styroyl | The 4-HO-benzyl | Methyl | (4-MeO-benzyl) amino | 558 | 559 |
| 204 | Styroyl | The 4-HO-benzyl | Methyl | Cyclohexyl amino | 520 | 521 |
| 205 | 2, the two phenylethyls of 2- | The 4-HO-benzyl | Methyl | (4-Me-phenyl) amino | 604 | 605 |
| 206 | 2, the two phenylethyls of 2- | The 4-HO-benzyl | Methyl | (4-Cl-phenyl) amino | 624 | 625 |
| 207 | 2, the two phenylethyls of 2- | The 4-HO-benzyl | Methyl | Phenyl amino | 590 | 591 |
| 208 | 2, the two phenylethyls of 2- | The 4-HO-benzyl | Methyl | ((R)-α-Jia Jibianji) amino | 618 | 619 |
| 209 | 2, the two phenylethyls of 2- | The 4-HO-benzyl | Methyl | Benzylamino | 604 | 605 |
| 210 | 2, the two phenylethyls of 2- | The 4-HO-benzyl | Methyl | (4-MeO-phenyl) amino | 620 | 621 |
| 211 | 2, the two phenylethyls of 2- | The HO-benzyl | Methyl | (4-Br-phenyl) amino | 669 | 670 |
| 212 | 2, the two phenylethyls of 2- | The 4-HO-benzyl | Methyl | (4-CF 3-phenyl) amino | 658 | 659 |
| 213 | 2, the two phenylethyls of 2- | The 4-HO-benzyl | Methyl | Amyl group amino | 584 | 585 |
| 214 | 2, the two phenylethyls of 2- | The 4-HO-benzyl | Methyl | (2-phenylethyl) amino | 618 | 619 |
| 215 | 2, the two phenylethyls of 2- | The 4-HO-benzyl | Methyl | (4-MeO-benzyl) amino | 634 | 635 |
| 216 | 2, the two phenylethyls of 2- | The 4-HO-benzyl | Methyl | Cyclohexyl amino | 596 | 597 |
| 217 | Styroyl | 3，4-Cl 2-benzyl | Methyl | (4-MeO-phenyl) amino | 581 | 582 |
| 218 | Styroyl | 3，4-Cl 2-benzyl | Methyl | (4-Cl-phenyl) amino | 601 | 602 |
| 219 | Styroyl | 3，4-Cl 2-benzyl | Methyl | Phenyl amino | 556 | 567 |
| 220 | Styroyl | 3，4-Cl 2-benzyl | Methyl | ((R)-α-Jia Jibianji) amino | 595 | 596 |
| 221 | Styroyl | 3，4-Cl 2-benzyl | Methyl | Benzylamino | 581 | 582 |
| 222 | Styroyl | 3，4-Cl 2-benzyl | Methyl | (4-MeO-phenyl) amino | 597 | 598 |
| 223 | Styroyl | 3，4-Cl 2-benzyl | Methyl | (4-Br-phenyl) amino | 645 | 646 |
| 224 | Styroyl | 3，4-Cl 2-benzyl | Methyl | (4-CF 3-benzyl) amino | 634 | 635 |
| 225 | Styroyl | 3，4-Cl 2-benzyl | Methyl | Amyl group amino | 561 | 562 |
| 226 | Styroyl | 3，4-Cl 2-benzyl | Methyl | (2-benzyl ethyl) amino | 595 | 596 |
| 227 | Styroyl | 3，4-Cl 2-benzyl | Methyl | (4-MeO-benzyl) amino | 611 | 612 |
| 228 | Styroyl | 3，4-Cl 2-benzyl | Methyl | Cyclohexyl amino | 573 | 574 |
| 229 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | (4-Me-phenyl) amino | 657 | 658 |
| 230 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | (4-Cl-phenyl) amino | 677 | 678 |
| 231 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | Phenyl amino | 643 | 644 |
| 232 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | ((R)-α-Jia Jibianji) amino | 671 | 672 |
| 233 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | Benzylamino | 657 | 658 |
| 234 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | (4-MeO-phenyl) amino | 673 | 674 |
| 235 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | (4-Br-phenyl) amino | 721 | 722 |
| 236 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | (4-CF 3-phenyl) amino | 711 | 712 |
| 237 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | Amyl group amino | 637 | 638 |
| 238 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | (2-phenylethyl) amino | 671 | 672 |
| 239 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | (4-MeO-benzyl) amino | 687 | 688 |
| 240 | 2, the two phenylethyls of 2- | 3，4-Cl 2-benzyl | Methyl | Cyclohexyl amino | 649 | 650 |
| 241 | Isopentyl | The 4-HO-benzyl | Methyl | (4-Me-phenyl) amino | 478 | 479 |
| 242 | Isopentyl | The 4-HO-benzyl | Methyl | (4-Cl-phenyl) amino | 498 | 499 |
| 243 | Isopentyl | The 4-HO-benzyl | Methyl | Phenyl amino | 464 | 465 |
| 244 | Isopentyl | The 4-HO-benzyl | Methyl | ((R)-α-Jia Jibianji) amino | 492 | 493 |
| 245 | Isopentyl | The 4-HO-benzyl | Methyl | Benzylamino | 478 | 479 |
| 246 | Isopentyl | The 4-HO-benzyl | Methyl | (4-MeO-phenyl) amino | 494 | 495 |
| 247 | Isopentyl | The 4-HO-benzyl | Methyl | (4-Br-phenyl) amino | 542 | 543 |
| 248 | Isopentyl | The 4-HO-benzyl | Methyl | (4-CF 3-benzyl) amino | 532 | 533 |
| 249 | Isopentyl | The 4-HO-benzyl | Methyl | The amyl group chloro | 458 | 459 |
| 250 | Isopentyl | The 4-HO-benzyl | Methyl | (2-phenylethyl) amino | 492 | 493 |
| 251 | Isopentyl | The 4-HO-benzyl | Methyl | (4-MeO-benzyl) amino | 508 | 509 |
| 252 | Isopentyl | The 4-HO-benzyl | Methyl | Cyclohexyl amino | 470 | 471 |
| 253 | Isopentyl | The 4-HO-benzyl | Methyl | (4-Me-phenyl) amino | 554 | 555 |
| 254 | Isopentyl | The 4-HO-benzyl | Methyl | (4-Cl-phenyl) amino | 574 | 575 |
| 255 | Isopentyl | The 4-HO-benzyl | Methyl | Phenyl amino | 540 | 541 |
| 256 | Isopentyl | The 4-HO-benzyl | Methyl | ((R)-α-Jia Jibianji) amino | 568 | 569 |
| 257 | Isopentyl | The 4-HO-benzyl | Methyl | Benzylamino | 554 | 555 |
| 258 | Isopentyl | The 4-HO-benzyl | Methyl | (4-MeO-phenyl) amino | 570 | 571 |
| 259 | Isopentyl | The 4-HO-benzyl | Methyl | (4-Br-phenyl) amino | 619 | 620 |
| 260 | Isopentyl | The 4-HO-benzyl | Methyl | (4-CF 3-phenyl) amino | 608 | 609 |
| 261 | Isopentyl | The 4-HO-benzyl | Methyl | Amyl group amino | 534 | 535 |
| 262 | Isopentyl | The 4-HO-benzyl | Methyl | (2-phenylethyl) amino | 568 | 569 |
| 263 | Isopentyl | The 4-HO-benzyl | Methyl | (4-MeO-benzyl) amino | 584 | 585 |
| 264 | Isopentyl | The 4-HO-benzyl | Methyl | Cyclohexyl amino | 546 | 547 |
| 265 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-Me-phenyl) amino | 526 | 527 |
| 266 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-Cl-phenyl) amino | 546 | 547 |
| 267 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | Phenyl amino | 512 | 513 |
| 268 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | ((R)-α-Jia Jibianji) amino | 540 | 541 |
| 269 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | Benzylamino | 526 | 527 |
| 270 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-MeO-phenyl) amino | 542 | 543 |
| 271 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-Br-phenyl) amino | 591 | 592 |
| 272 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-CF 3-phenyl) amino | 580 | 581 |
| 273 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | Amyl group amino | 506 | 507 |
| 274 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (2-phenylethyl) amino | 540 | 541 |
| 275 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-MeO-benzyl) amino | 556 | 557 |
| 276 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | Cyclohexyl amino | 518 | 519 |
| 277 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-Me-phenyl) amino | 602 | 603 |
| 278 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-Cl-phenyl) amino | 622 | 623 |
| 279 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | Phenyl amino | 588 | 589 |
| 280 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | ((R)-α-Jia Jibianji) amino | 616 | 617 |
| 281 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | Benzylamino | 602 | 603 |
| 282 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-MeO-phenyl) amino | 618 | 619 |
| 283 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-Br-phenyl) amino | 667 | 668 |
| 284 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-CF 3-phenyl) amino | 656 | 657 |
| 285 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | Amyl group amino | 582 | 583 |
| 286 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (2-phenylethyl) amino | 616 | 617 |
| 287 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | (4-MeO-benzyl) amino | 632 | 633 |
| 288 | The 4-methyl-benzyl | 3，4-Cl 2-benzyl | Methyl | Cyclohexyl amino | 594 | 595 |
| 289 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | (N-Cbz-3-indoles ethyl) amino | 751 | 752 |
| 290 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | (naphthalene-2-ylmethyl) amino | 614 | 615 |
| 291 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | (2-phenylethyl) amino | 578 | 579 |
| 292 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | [2-(4-MeO-phenyl) ethyl] amino | 608 | 609 |
| 293 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | (3-CF 3-benzyl) amino | 632 | 633 |
| 294 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | (4-MeO-benzyl) amino | 594 | 595 |
| 295 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | (4-F-phenylethyl) amino | 596 | 597 |
| 296 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | (3，4Cl 2-benzyl) amino | 633 | 634 |
| 297 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | (2-HO-ethyl) amino | 518 | 519 |
| 298 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | (3-MeO-propyl group) amino | 546 | 547 |
| 299 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | (tetrahydrofuran (THF)-2-ylmethyl) amino | 558 | 559 |
| 300 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Methyl | (cyclohexylmethyl) amino | 570 | 571 |
| 301 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | (N-Cbz-3-indoles ethyl) amino | 779 | 780 |
| 302 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | (naphthalene-2-ylmethyl) amino | 642 | 643 |
| 303 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | (2-phenylethyl) amino | 606 | 607 |
| 304 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | [2-(4-MeO-phenyl) ethyl] amino | 636 | 637 |
| 305 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | (3-CF 3-benzyl) amino | 660 | 661 |
| 306 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | (4-MeO-benzyl) amino | 622 | 623 |
| 307 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | (4-F-phenylethyl) amino | 624 | 625 |
| 308 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | (3，4-Cl 2-benzyl) amino | 661 | 662 |
| 309 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | (2-HO-ethyl) amino | 546 | 547 |
| 310 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | (3-MeO-propyl group) amino | 574 | 575 |
| 311 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | (tetrahydrofuran (THF)-2-ylmethyl) amino | 586 | 587 |
| 312 | Naphthalene-1-ylmethyl | The 4-HO-benzyl | Propyl group | (cyclohexylmethyl) amino | 598 | 599 |
| 313 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | (N-Cbz-3-indoles ethyl) amino | 771 | 772 |
| 314 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | (naphthalene-2-ylmethyl) amino | 634 | 635 |
| 315 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | (2-phenylethyl) amino | 598 | 599 |
| 316 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | [2-(4-MeO-phenyl) ethyl] amino | 628 | 659 |
| 317 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | (3-CF 3-benzyl) amino | 652 | 653 |
| 318 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | (4-MeO-benzyl) amino | 614 | 615 |
| 319 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | (4-F-phenylethyl) amino | 616 | 617 |
| 320 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | (3，4-Cl 2-benzyl) amino | 653 | 654 |
| 321 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | (2-HO-ethyl) amino | 538 | 539 |
| 322 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | (3-MeO-propyl group) amino | 566 | 567 |
| 323 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | (tetrahydrofuran (THF)-2-ylmethyl) amino | 578 | 579 |
| 324 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Methyl | (cyclohexylmethyl) amino | 590 | 591 |
| 325 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | (N-Chz-3-indoles ethyl) amino | 779 | 800 |
| 326 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | (naphthalene-2-ylmethyl) amino | 662 | 663 |
| 327 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | (2-phenylethyl) amino | 626 | 627 |
| 328 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | [2-(4-MeO-phenyl) ethyl] amino | 656 | 657 |
| 329 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | (3-CF 3-benzyl) amino | 680 | 681 |
| 330 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | (4-MeO-benzyl) amino | 642 | 643 |
| 331 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | (4-F-phenylethyl) amino | 644 | 645 |
| 332 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | (3，4-Cl 2-benzyl) amino | 681 | 682 |
| 333 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | (2-HO-ethyl) amino | 566 | 567 |
| 334 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | (3-MeO-propyl group) amino | 594 | 595 |
| 335 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | (tetrahydrofuran (THF)-2-ylmethyl) amino | 606 | 607 |
| 336 | Naphthalene-1-ylmethyl | 3，4-F 2-benzyl | Propyl group | (cyclohexylmethyl) amino | 618 | 619 |
| 337 | Naphthalene-1-ylmethyl | 4-xenyl-methyl | Methyl | (N-Cbz-3-indoles ethyl) amino | 811 | 812 |
| 338 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Methyl | (naphthalene-2-ylmethyl) amino | 674 | 675 |
| 339 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Methyl | (2-phenylethyl) amino | 638 | 639 |
| 340 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Methyl | [2-(4-MeO-phenyl) ethyl] amino | 668 | 669 |
| 341 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Methyl | (3-CF 3-benzyl) amino | 692 | 693 |
| 342 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Methyl | (4-MeO-benzyl) amino | 654 | 655 |
| 343 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Methyl | (4-F-phenylethyl) amino | 656 | 657 |
| 344 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Methyl | (3, the 4-Cl-benzyl) amino | 693 | 694 |
| 345 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Methyl | (2-HO-ethyl) amino | 578 | 579 |
| 346 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Methyl | (3-MeO-propyl group) amino | 606 | 607 |
| 347 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Methyl | (tetrahydrofuran (THF)-2-ylmethyl) amino | 618 | 619 |
| 348 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Methyl | (cyclohexyl methyl) amino | 630 | 631 |
| 349 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | (N-Cbz-3-indoles ethyl) amino | 839 | 840 |
| 350 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | (naphthalene-2-ylmethyl) amino | 702 | 703 |
| 351 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | (2-phenylethyl) amino | 666 | 667 |
| 352 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | [2-(4-MeO-phenyl) ethyl] amino | 696 | 697 |
| 353 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | (3-CF 3-benzyl) amino | 720 | 721 |
| 354 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | (4-MeO-benzyl) amino | 682 | 683 |
| 355 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | (4-F-phenylethyl) amino | 684 | 685 |
| 356 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | (3，4-Cl 2-benzyl) amino | 721 | 722 |
| 357 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | (2-HO-ethyl) amino | 606 | 607 |
| 358 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | (3-MeO-propyl group) amino | 634 | 635 |
| 359 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | (tetrahydrofuran (THF)-2-ylmethyl) amino | 646 | 647 |
| 360 | Naphthalene-1-ylmethyl | 4-xenyl methyl | Propyl group | (cyclohexyl methyl) amino | 658 | 659 |
| 361 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | (N-Cbz-3-indyl) amino | 807 | 808 |
| 362 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | (naphthalene-2-ylmethyl) amino | 670 | 671 |
| 363 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | (2-phenylethyl) amino | 634 | 635 |
| 364 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | [2-(4-MeO-phenyl)] amino | 664 | 665 |
| 365 | Naphthalene-1-ylmethyl | The 3-t-Bu-HO-benzyl | Methyl | (3-CF 3-benzyl) amino | 688 | 689 |
| 366 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | (4-MeO-benzyl) amino | 650 | 651 |
| 367 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | (4-F-phenylethyl) amino | 652 | 653 |
| 368 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | (3，4-Cl 2-benzyl) amino | 689 | 690 |
| 369 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | (2-HO-ethyl) amino | 574 | 575 |
| 370 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | (3-MeO-propyl group) amino | 602 | 603 |
| 371 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | (tetrahydrofuran (THF)-2-ylmethyl) amino | 614 | 615 |
| 372 | Naphthalene 1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | (cyclohexyl methyl) amino | 626 | 627 |
| 373 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | (N-Cbz-3-indoles ethyl) amino | 835 | 836 |
| 374 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | (naphthalene-2-ylmethyl) amino | 698 | 699 |
| 375 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | (2-phenylethyl) amino | 662 | 663 |
| 376 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | [2-(4-MeO-benzyl) ethyl] amino | 692 | 693 |
| 377 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | (3-CF 3-benzyl) amino | 716 | 717 |
| 378 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | (4-MeO-benzyl) amino | 678 | 679 |
| 379 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | (4-F-phenylethyl) amino | 680 | 681 |
| 380 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | (3，4-Cl 2-benzyl) amino | 717 | 718 |
| 381 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | (2-HO-ethyl) amino | 602 | 603 |
| 382 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | (3-MeO-propyl group) amino | 630 | 631 |
| 383 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | (tetrahydrofuran (THF)-2-ylmethyl) amino | 642 | 643 |
| 384 | Naphthalene-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Propyl group | (cyclohexyl methyl) amino | 654 | 655 |
| 385 | The 4-methoxy-benzyl | OCH 3 | The 5-F-benzyl | OCH 3 | 470 | 471 |
| 386 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | The styryl methyl | OCH 3 | 591 | 592 |
| 387 | Naphthyl-1-ylmethyl | 4-NO 2-benzyl | The styryl methyl | OCH 3 | 620 | 621 |
| 388 | Naphthyl-1-ylmethyl | 3，4-F 2-benzyl | The styryl methyl | OCH 3 | 611 | 612 |
| 389 | Naphthyl-1-ylmethyl | The 4-Cl-benzyl | The styryl methyl | OCH 3 | 609 | 610 |
| 390 | Naphthyl-1-ylmethyl | 4-benzyl-benzyl | The styryl methyl | OCH 3 | 651 | 652 |
| 391 | Naphthyl-1-ylmethyl | The 3-t-Bu-4-HO benzyl | The styryl methyl | OCH 3 | 647 | 648 |
| 392 | Naphthyl-1-ylmethyl | 4-methyl-benzyl | The styryl methyl | OCH 3 | 589 | 590 |
| 393 | Naphthyl-1-ylmethyl | Cyclohexyl methyl | The styryl methyl | OCH 3 | 581 | 582 |
| 394 | Naphthyl-1-ylmethyl | The 4-F-benzyl | The styryl methyl | OCH 3 | 593 | 594 |
| 395 | Naphthyl-1-ylmethyl | The 2-Cl-benzyl | The styryl methyl | OCH 3 | 609 | 610 |
| 396 | Naphthyl-1-ylmethyl | 3，4-Cl 2-benzyl | The styryl methyl | OCH 3 | 644 | 645 |
| 397 | Naphthyl-1-ylmethyl | Naphthyl-1-ylmethyl | The styryl methyl | OCH 3 | 625 | 626 |
| 398 | 3，4-Cl 2-benzyl | The 4-HO-benzyl | The styryl methyl | OCH 3 | 610 | 611 |
| 399 | 3，4-Cl 2-benzyl | 4-NO 2-benzyl | The styryl methyl | OCH 3 | 639 | 640 |
| 400 | 3，4-Cl 2-benzyl | 3，4-F 2-benzyl | The styryl methyl | OCH 3 | 629 | 630 |
| 401 | 3，4-Cl 2-benzyl | The 4-Cl-benzyl | The styryl methyl | OCH 3 | 628 | 629 |
| 402 | 3，4-Cl 2-benzyl | 4-phenyl-benzyl | The styryl methyl | OCH 3 | 670 | 671 |
| 403 | 3，4-Cl 2-benzyl | The 3-t-Bu-4-HO-benzyl | The styryl methyl | OCH 3 | 666 | 667 |
| 404 | 3，4-Cl 2-benzyl | 4-methyl-benzyl | The styryl methyl | OCH 3 | 608 | 609 |
| 405 | 3，4-Cl 2-benzyl | Cyclohexyl methyl | The styryl methyl | OCH 3 | 600 | 601 |
| 406 | 3，4-Cl 2-benzyl | The 4-F-benzyl | The styryl methyl | OCH 3 | 611 | 612 |
| 407 | 3，4-Cl 2-benzyl | The 2-Cl-benzyl | The styryl methyl | OCH 3 | 628 | 629 |
| 408 | 3，4-Cl 2-benzyl | 3，4-Cl 2-benzyl | The styryl methyl | OCH 3 | 662 | 663 |
| 409 | 3，4-Cl 2-benzyl | Naphthyl-1-ylmethyl | The styryl methyl | OCH 3 | 644 | 645 |
| 410 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 634 | 635 |
| 411 | Naphthyl-1-ylmethyl | 4-NO 2Benzyl | 2，6-Cl 2-benzyl | OCH 3 | 663 | 664 |
| 412 | Naphthyl-1-ylmethyl | 3，4-F 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 654 | 655 |
| 413 | Naphthyl-1-ylmethyl | The 4-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 652 | 653 |
| 414 | Naphthyl-1-ylmethyl | 4-phenyl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 694 | 695 |
| 415 | Naphthyl-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 690 | 691 |
| 416 | Naphthyl-1-ylmethyl | 4-methyl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 632 | 633 |
| 417 | Naphthyl-1-ylmethyl | Cyclohexyl methyl | 2，6-Cl 2-benzyl | OCH 3 | 624 | 625 |
| 418 | Naphthyl-1-ylmethyl | The 4-F-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 636 | 637 |
| 419 | Naphthyl-1-ylmethyl | The 2-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 652 | 653 |
| 420 | Naphthyl-1-ylmethyl | 3, the 4-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 686 | 687 |
| 421 | Naphthyl-1-ylmethyl | Naphthyl-1-ylmethyl | 2，6-Cl 2-benzyl | OCH 3 | 668 | 669 |
| 422 | 3，4-Cl 2-benzyl | The 4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 652 | 653 |
| 423 | 3，4-Cl 2-benzyl | 4-NO 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 681 | 682 |
| 424 | 3，4-Cl 2-benzyl | 3，4-F 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 672 | 673 |
| 425 | 3，4-Cl 2-benzyl | The 4-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 671 | 672 |
| 426 | 3，4-Cl 2-benzyl | 4-phenyl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 712 | 713 |
| 427 | 3，4-Cl 2-benzyl | The 3-t-Bu-4-HO-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 708 | 709 |
| 428 | 3，4-Cl 2-benzyl | 4-methyl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 650 | 651 |
| 429 | 3，4-Cl 2-benzyl | Cyclohexyl methyl | 2，6-Cl 2-benzyl | OCH 3 | 642 | 643 |
| 430 | 3，4-Cl 2-benzyl | The 4-F-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 654 | 655 |
| 431 | 3，4-Cl 2-benzyl | The 2-Cl-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 671 | 672 |
| 432 | 3，4-Cl 2-benzyl | 3，4-Cl 2-benzyl | 2，6-Cl 2-benzyl | OCH 3 | 705 | 706 |
| 433 | 3，4-Cl 2-benzyl | Naphthyl-1-ylmethyl | 2，6-Cl 2-benzyl | OCH 3 | 686 | 687 |
| 434 | 2-piperidines-1-base-ethyl | (S)-the 4-HO-benzyl | Methyl | Benzylamino | 535 | 536 |
| 435 | 3，4-Cl 2-benzyl | (S)-the 4-HO-benzyl | Methyl | 2-piperidines-1-ethylamino | 604 | 605 |
| 436 | 3，4-Cl 2-benzyl | (S)-the 4-HO-benzyl | Methyl | 2-(1-methyl-tetramethyleneimine-2-yl)-ethylamino | 604 | 605 |
| 437 | The 3-pyridylmethyl | (S)-the 4-HO-benzyl | Methyl | 3, the 4-Cl-benzylamino | 583 | 584 |
| 438 | 2-morpholine-4-base-ethyl | (S)-the 4-HO-benzyl | Methyl | 3，4-Cl 2-benzylamino | 606 | 607 |
| 439 | 3，4-Cl 2-benzyl | (S)-the 4-HO-benzyl | Methyl | 3-pyridylmethyl amino | 583 | 584 |
| 440 | 3，4-Cl 2-benzyl | (S)-the 4-HO-benzyl | Methyl | 2-morpholine-4-base ethylamino | 606 | 607 |
| 441 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 3-imidazoles-1-base-propyl group amino | 582 | 583 |
| 442 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 4-amino-benzene ethylamino | 593 | 594 |
| 443 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 3-pyridylmethyl amino | 565 | 566 |
| 444 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 2-(3-pyridyl ethyl) amino | 579 | 580 |
| 445 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 4-pyridylmethyl amino | 565 | 566 |
| 446 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Benzyloxycarbonyl amino | 622 | 623 |
| 447 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | The 4-F-benzylamino | 582 | 583 |
| 448 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 4-CO 2The H-benzylamino | 608 | 609 |
| 449 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 4-CF 3-benzylamino | 632 | 633 |
| 450 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | (S)-alpha-methyl-benzyl amino | 578 | 579 |
| 451 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | (R)-alpha-methyl-benzyl amino | 578 | 579 |
| 452 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | The 2-F-benzylamino | 582 | 583 |
| 453 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 2,3-dimethoxy-benzyl amino | 624 | 625 |
| 454 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Cyano methyl amino | 513 | 514 |
| 455 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | The phenyl diazanyl | 565 | 566 |
| 456 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 4-aminobenzyl amino | 579 | 580 |
| 457 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | (S, S) 2-[(2-hydroxyl-1-methyl-2-phenyl-ethyl)-methyl-formamyl]-ethyl }-amino | 693 | 694 |
| 458 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | [4-(1,3-dioxo-1,3-dihydro-isoindole-2-ylmethyl) cyclohexyl]-methylamino | 715 | 716 |
| 459 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Indane-1-base is amino | 590 | 591 |
| 460 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Phenylglycocoll | 622 | 623 |
| 461 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 2，6-F 2-benzylamino | 600 | 601 |
| 462 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 3-F-benzyl amino | 582 | 583 |
| 463 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Benzimidazolyl-2 radicals-Ji-amino | 604 | 605 |
| 464 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Diphenyl-methyl amino | 640 | 641 |
| 465 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Furans-2-base-methylamino | 554 | 555 |
| 466 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 4-dimethylamino-benzylamino | 607 | 608 |
| 467 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Thio-furan-2-base-methylamino | 584 | 585 |
| 468 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 4-NO 2-benzylamino | 609 | 610 |
| 469 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | BnO | 565 | 566 |
| 470 | 4-methoxyl group-naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 594 | 595 |
| 471 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Styroyl | 563 | 564 |
| 472 | Naphthyl-1-ylmethyl | 4-methoxyl group-benzyl | Methyl | Benzylamino | 578 | 579 |
| 473 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | 4-CF 3-phenyl amino | 618 | 619 |
| 474 | Naphthyl-1-ylmethyl | 4-NO 2-benzyl | Methyl | 4-CF 3-phenyl amino | 647 | 648 |
| 475 | Naphthyl-1-ylmethyl | 4-NO 2-benzyl | Methyl | Benzyl-amino | 593 | 594 |
| 476 | Benzyl | Naphthyl-1-ylmethyl | The 4-CN-benzyl | OCH 3 | 574 | 575 |
| 477 | Thio-furan-2-base-methyl | Naphthyl-1-ylmethyl | The 4-CN-benzyl | OCH 3 | 594 | 595 |
| 478 | 4-dimethylamino base-benzyl | Naphthyl-1-ylmethyl | The 4-CN-benzyl | OCH 3 | 617 | 618 |
| 479 | Styroyl | Naphthyl-1-ylmethyl | The 4-CN-benzyl | OCH 3 | 588 | 589 |
| 480 | 8-quinoline-1-base-methyl | The 4-HO-benzyl | Methyl | Benzylamino | 565 | 566 |
| 481 | The 4-pyridylmethyl | Naphthyl-1-ylmethyl | Benzyl | OCH 3 | 550 | 551 |
| 482 | 3, the 4-dimethoxy-benzyl | Naphthyl-1-ylmethyl | Benzyl | OCH 3 | 609 | 610 |
| 483 | 3,4-dimethoxy-styroyl | Naphthyl-1-ylmethyl | Benzyl | OCH 3 | 623 | 624 |
| 484 | Thio-furan-2-base-methyl | Naphthyl-1-ylmethyl | Benzyl | OCH 3 | 569 | 570 |
| 485 | Naphthyl-1-ylmethyl | The 3-pyridylmethyl | Methyl | Benzylamino | 549 | 550 |
| 486 | Naphthyl-1-ylmethyl | PFBBR | Methyl | Benzylamino | 638 | 639 |
| 487 | Naphthyl-1-ylmethyl | The 3-F-4-HO-benzyl | Methyl | Benzylamino | 582 | 583 |
| 488 | The 4-F-styroyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 598 | 599 |
| 489 | 4-anisole ethyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 610 | 611 |
| 490 | 3,4-dimethoxy-styroyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 640 | 641 |
| 491 | Naphthyl-1-ylmethyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 616 | 617 |
| 492 | 3, the 4-dimethoxy-benzyl | Naphthyl-1-ylmethyl | The 4-CN-benzyl | OCH 3 | 634 | 635 |
| 493 | 3,4-dimethyl-styroyl | Naphthyl-1-ylmethyl | The 4-CN-benzyl | OCH 3 | 648 | 649 |
| 494 | 4-quinoline-1-base-methyl | The 4-HO-benzyl | Methyl | Benzylamino | 565 | 566 |
| 495 | The 2-pyridylmethyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 567 | 568 |
| 496 | The 3-pyridylmethyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 567 | 568 |
| 497 | 3, the 4-dimethoxy | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 626 | 627 |
| 498 | 4-methyl-benzyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 580 | 581 |
| 499 | Thio-furan-2-base-methyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 572 | 573 |
| 500 | 4-CF 3-benzyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 634 | 635 |
| 501 | 2，6-F 2-benzyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 602 | 603 |
| 502 | The 4-F-benzyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 584 | 585 |
| 503 | Thio-furan-2-base-ethyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 586 | 587 |
| 504 | 3，4-Cl 2-benzyl | 4-methyl-benzyl | Methyl | 4-CF 3-phenyl amino | 634 | 635 |
| 505 | 4-CO 2The H-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 558 | 559 |
| 506 | Naphthyl-1-ylmethyl | The 3-t-Bu-4-HO-benzyl | Methyl | Benzylamino | 620 | 621 |
| 507 | Naphthyl-1-ylmethyl | 3，4-(OH) 2-benzyl | Methyl | Benzylamino | 580 | 581 |
| 508 | The 2-F-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 532 | 533 |
| 509 | The 3-F-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 532 | 533 |
| 510 | The 4-F-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 532 | 533 |
| 511 | 2，4-F 2-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 550 | 551 |
| 512 | 2，6-F 2-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 550 | 551 |
| 513 | 2，5-F 2-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 550 | 551 |
| 514 | 3-CF 3-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 582 | 583 |
| 515 | 4-CF 3-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 582 | 583 |
| 516 | 3，4，5-F 3-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 568 | 569 |
| 517 | The 2-Cl-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 548 | 549 |
| 518 | The 3-Cl-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 548 | 549 |
| 519 | 2，4-Cl 2-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 582 | 583 |
| 520 | (S)-aminomethyl phenyl | The 4-HO-benzyl | Methyl | Benzylamino | 528 | 529 |
| 521 | (R)-aminomethyl phenyl | The 4-HO-benzyl | Methyl | Benzylamino | 528 | 529 |
| 522 | 4-methyl-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 528 | 529 |
| 523 | The 4-methoxy-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 544 | 545 |
| 524 | 3, the 4-dimethoxy-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 574 | 575 |
| 525 | Furans-2-base-methylamino | The 4-HO-benzyl | Methyl | Benzylamino | 504 | 505 |
| 526 | (R)-methyl naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 578 | 579 |
| 527 | (S)-methyl naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 578 | 579 |
| 528 | Naphthyl-1-ylmethyl | 3-oxygen-pyridine-1-ylmethyl | Methyl | Benzylamino | 565 | 566 |
| 529 | (R)-the alpha-methyl-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 578 | 579 |
| 530 | Naphthyl-2-ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 564 | 565 |
| 531 | 4-F-naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 582 | 583 |
| 532 | The 2-methoxy-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 544 | 545 |
| 533 | The 4-Cl-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 548 | 549 |
| 534 | 3，4-Cl 2-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 582 | 583 |
| 535 | 2-CF 3The O benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 598 | 599 |
| 536 | 2-CF 3The S benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 614 | 615 |
| 537 | 2-CF 3Benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 582 | 583 |
| 538 | 5-quinoline-1-base-methyl | The 4-HO-benzyl | Methyl | Benzylamino | 565 | 566 |
| 539 | 8-quinoline-1-base-methyl | The 3-t-Bu-4-HO-benzyl | Methyl | Benzylamino | 621 | 622 |
| 540 | 8-quinoline-1-base-methyl | 4-NO 2-benzyl | Methyl | Benzylamino | 594 | 595 |
| 541 | 8-quinoline-1-base-methyl | (1H-pyrroles-2-base-)-methyl | Methyl | Benzylamino | 538 | 539 |
| 542 | Naphthyl-1-base-methyl | 4-benzyloxy-carbonylamino benzyl | Methyl | Benzylamino | 697 | 698 |
| 543 | 2，3-Cl 2-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 582 | 583 |
| 544 | PFBBR | The 4-HO-benzyl | Methyl | Benzylamino | 604 | 605 |
| 545 | Benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 514 | 515 |
| 546 | Quinoxaline-5-base-methyl | The 4-HO-benzyl | Methyl | Benzylamino | 566 | 567 |
| 547 | 8-quinoline-1-base-methyl | The 3-pyridylmethyl | Methyl | Benzylamino | 550 | 551 |
| 548 | 8-quinoline-1-base-methyl | PFBBR | Methyl | Benzylamino | 639 | 640 |
| 549 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino (thiocarbamide) | 580 | 581 |
| 550 | Naphthyl-1-ylmethyl | 4-amino-benzyl | Methyl | Benzylamino | 563 | 564 |
| 551 | 3,4,5-trimethoxy benzyl | 4-amino-benzyl | Methyl | Benzylamino | 603 | 604 |
| 552 | Naphthyl-1-ylmethyl | The 4-pyridylmethyl | Methyl | Benzylamino | 549 | 550 |
| 553 | Naphthyl-1-ylmethyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 550 | 551 |
| 554 | 2-HO-3-methoxyl group-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 560 | 561 |
| 555 | Naphthyl-1-ylmethyl | 3-nitro-4-HO-benzyl | Methyl | Benzylamino | 609 | 610 |
| 556 | Naphthyl-1-ylmethyl | 4-CO 2H-CH 2The O-benzyl | Methyl | Benzylamino | 622 | 623 |
| 557 | Naphthyl-1-ylmethyl | 1-naphthoyl base amino-methyl | Methyl | Benzylamino | 641 | 642 |
| 558 | Naphthyl-1-ylmethyl | 4-Oxopyridyl methyl | Methyl | Benzylamino | 565 | 566 |
| 559 | The 4-F-alpha-methyl-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 546 | 547 |
| 560 | Naphthyl-1-ylmethyl | The benzoyl-amido ethyl | Methyl | Benzylamino | 605 | 606 |
| 561 | 8-quinoline-1-base-methyl | 3，4-(OH) 2-benzyl | Methyl | Benzylamino | 581 | 582 |
| 562 | 4-N, N-dimethylamino-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 557 | 558 |
| 563 | Naphthyl-1-ylmethyl | (R) 4-F-benzyl | Methyl | Benzylamino | 609 | 610 |
| 564 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | The 2-chloroethyl amino | 536 | 537 |
| 565 | Naphthyl-1-ylmethyl | The 4-HO-styroyl | Methyl | Benzylamino | 578 | 579 |
| 566 | The 4-F-benzyl | 3-F, the 4-HO-benzyl | Methyl | Benzylamino | 550 | 551 |
| 567 | 2，4-F 2-benzyl | 3-F, the 4-HO-benzyl | Methyl | Benzylamino | 568 | 569 |
| 568 | 3-CF 3Benzyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 568 | 569 |
| 569 | (S)-methyl naphthyl-1-ylmethyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 514 | 515 |
| 570 | (R)-methyl naphthyl-1-ylmethyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 514 | 515 |
| 571 | 2，3，6-F 3-benzyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 554 | 555 |
| 572 | The 3-F-benzyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 518 | 519 |
| 573 | The 4-Cl-benzyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 534 | 535 |
| 574 | The 3-Cl-benzyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 534 | 535 |
| 575 | The 2-Cl-benzyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 534 | 535 |
| 576 | 3，4-Cl 2-benzyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 568 | 569 |
| 577 | 3-CF 3The O-benzyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 584 | 585 |
| 578 | The 4-F-benzyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 518 | 519 |
| 579 | 2，4-F 2-benzyl | (R) 4-HO-phenyl | Methyl | Benzylamino | 536 | 537 |
| 580 | 3-(2-chloro-ethyl)-urea groups]-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 634 | 635 |
| 581 | The 3-aminobenzyl | The 4-HO-benzyl | Methyl | Benzylamino | 529 | 530 |
| 582 | 3-N-methylamino benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 543 | 544 |
| 583 | 3-N, N-dimethylamino benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 557 | 558 |
| 584 | 1H-benzoglyoxaline-4-ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 554 | 555 |
| 585 | The 2-HO-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 530 | 531 |
| 586 | The 2-picolyl | The 4-HO-benzyl | Methyl | Benzylamino | 515 | 516 |
| 587 | The 4-pyridylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 515 | 516 |
| 588 | 8-quinoline-2-ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 565 | 566 |
| 289 | 8-cumarone-4-ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 554 | 555 |
| 590 | Naphthyl-1-ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 550 | 551 |
| 591 | The 4-F-benzyl | The 4-HO-phenyl | Methyl | Benzylamino | 518 | 519 |
| 592 | 2，4-F 2-benzyl | The 4-HO-phenyl | Methyl | Benzylamino | 536 | 537 |
| 593 | (R)-the toluyl ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 542 | 543 |
| 594 | (S)-the toluyl ylmethyl | The 4-HO-benzyl | Methyl | Benzylamino | 542 | 543 |
| 595 | 1,2,3,4-four-hydrogen-naphthalene-2-base | The 4-HO-benzyl | Methyl | Benzylamino | 554 | 555 |
| 596 | Naphthyl-1-ylmethyl | 3, the 4-dimethoxy-benzyl | Methyl | Benzylamino | 608 | 609 |
| 597 | 2-dimethylamino-6-F-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 575 | 576 |
| 598 | 2-dimethylamino benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 557 | 558 |
| 599 | Naphthyl-1-ylmethyl | The 4-CN-benzyl | Methyl | Benzylamino | 573 | 574 |
| 600 | 4-F-2-CF 3-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 599 | 600 |
| 601 | 4-Cl-2-dimethylamino benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 591 | 592 |
| 602 | 3-N, N-ethylmethylamino-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 571 | 572 |
| 603 | 3-diethylin benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 585 | 586 |
| 604 | 4-Cl-3-dimethylamino benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 591 | 592 |
| 605 | 4-F-2-dimethylamino benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 575 | 576 |
| 606 | 3，5-(CH 3) 2-2-dimethylamino-benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 585 | 586 |
| 607 | 3-(CH 3)-2-dimethylamino benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 571 | 572 |
| 608 | 6-(CH 3)-2-dimethylamino benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 571 | 572 |
| 609 | 3，4-F 2-2-dimethylamino benzyl | The 4-HO-benzyl | Methyl | Benzylamino | 593 | 594 |
In addition, the synthetic of the peptide mimics in library of the present invention can adopt the general route in following [4,3,0] reverse turn mimetics library to finish.
The FlexChem Reactor Block that the synthetic use of the peptide mimics in two ring template libraries of the present invention has 96 hole flat boards finishes by known technology.In above route, ' Pol ' represents bromoacetal resin (Advanced ChemTech), and detailed process such as following.
Step 1
The solution (2M solution) of bromoacetal resin (1.6mmol/g) and the R1 amine in DMSO is placed 96 hole Robbins block (FlexChem).Reaction mixture is used rotary oven [Robbins Scientific] vibration 12 hours down in 60 ℃.With DMF, MeOH washing resin, wash with DCM then.
Step 2
The solution of the Fmoc amino acid that is available commercially (4 equivalent), PyBob (4 equivalent), HOAt (4 equivalent) and DIEA (12 equivalent) that will be in DMF is added to resin.Reaction mixture, with DMF, MeOH washing resin, is being washed with DCM after 12 hours then in vibration under the room temperature.
Step 3
Preceding toward reaction by being added in 25% piperidines among the DMF in the DMF swollen resin.In that reaction mixture is repeated this deprotection steps in vibration under the room temperature after 30 minutes once more, use DMF, methanol wash resin then, wash with DCM then.The solution of hydrazine urea chloride (4 equivalent), HOBt (4 equivalent) and DIC (4 equivalent) that will be in DMF is added to resin.Reaction mixture, with DMF, MeOH washing resin, is being washed with DCM after 12 hours then in vibration under the room temperature.
Step 4
Preceding toward reaction by being added in 25% piperidines among the DMF in the DMF swollen resin.In that reaction mixture is repeated this deprotection steps in vibration under the room temperature after 30 minutes once more, use DMF, methanol wash resin then, wash with DCM then.R that will be in DCM
1-isocyanic ester (5 equivalent) passes through DCM swollen resin before being added to reaction.Reaction mixture, with DMF, MeOH washing resin, is being washed with DCM after 12 hours then in vibration under the room temperature.
Step 5
Under the room temperature with formic acid (the every hole of 1.2mL) with plastic resin treatment 18 hours.After removing by filter resin, use SpeedVac[SAVANT] concentrating under reduced pressure filtrate obtains product, is oil.With 50% water/dilution in acetonitrile product, then in freezing back freeze-drying.
Table 3 has shown can [4,3,0] prepared in accordance with the present invention reverse turn mimetics library, and its representational preparation such as embodiment 5 provide.
Reverse turn mimetics library, [table 3] [4,3,0]
In the present invention further on the other hand, the biological activity in screening library and isolating biologically active library member's method are disclosed.Biological activity is screened by multiple technologies and method in library of the present invention.Usually, screening is analyzed and can followingly be carried out: (1) makes the stand-in in library contact with interested biological target body such as acceptor, so that between the stand-in in library and the target body combination takes place, (2) by people (Nature 354:82-84 such as suitable analysis such as Lam, 1991) or the disclosed calorimetric analysis of people (Biotechnology 12:1008-1011,1994) (quoting these two here as a reference) such as Griminski detect binding events.In a preferred embodiment, the library member is in solution and target body is fixed on the solid phase.Selectively, the library can be fixed on solid phase, and can survey by it is contacted with target body in the solution.
Following table 4 shows compound that is used for biological activity test and the IC thereof that selects from library of the present invention
50Value, described IC
50Value is by embodiment 6 described reporter gene assay determinations.
The IC of [table 4] selected library compound
50(μ M)
Find the compound of general formula (I) in the present invention, particularly the compound of general formula (VI) be because its specificity can suppress the transcription activating of the cancer cells of CBP mediation in conjunction with CBP, and it obtains the support of the CBP and the compound generation immunoprecipitation of the present invention of SW480 cell.
Compound of the present invention can also suppress the intracellular survivin of SW480 expresses, thus the carcinogenic activity of anticancer.Compound of the present invention can be used for anticancer, thereby can be used to regulate the cell growth.What support these results is, compound of the present invention shows further that also it can induce the caspase-3 activation in the SW480 cell, thus in cell apoptotic activity.Compound of the present invention can also be advantageously used in the apoptosis of inducing cell.
Be the carcinogenic activity of proof cancer cells, carry out external MTS cytotoxicity analysis test by the following method.
Cell toxicity test
SW480 or HCT116 cell are placed 96 hole microplates (10
4Cells/well), and at 37 ℃ cultivated 24 hours down.TCF4 compound pair cell with different concns was handled 24 hours.20 μ l MTS solution (Promega) are added to every hole, and cultivated 2 hours down at 37 ℃.Measure cell survival by using microplate to read the light absorption ratio that plate device (Molecular Device) reads under the 490nm, and calculate the cytotoxicity of every kind of concentration compound.
Growth-inhibiting is analyzed:
SW480 or HCT116 cell are placed 96 hole microplates (10
4Cells/well), and at 37 ℃ cultivated 24 hours down.With 20 μ l [3-(4,5-dimethylthiazole-2-yl)-5-(3-carboxyl phenyl)-2-(4-sulfophenyl)-2H-tetrazolium , inner salt] (MTS) solution (Promega) be added to every hole, and after cultivating 2 hours under 37 ℃, read light absorption ratio (negative control), handled 48 hours with the TCF4 compound pair cell of different concns then.20 μ l MTS solution (Promega) are added to every hole, and cultivated 2 hours down at 37 ℃.Under 490nm, read light absorption ratio and measure cell survival by using microplate to read plate device (Molecular Device), and calculate the cytotoxicity of every kind of concentration compound.
The result of the carcinogenic activity of selected library compound is as shown in table 5.
[table 5] is by carrying out the carcinogenic activity that the analyses of MTS or sulphur rhodamine B (sulforhodamine B) obtain to selected library compound
In another aspect of this invention, a kind of have general formula pharmaceutical composition of compound of compound, particularly general formula (VI) of (I) of comprising is disclosed.For the preparation of drug combination that contains The compounds of this invention, those skilled in the art can use known knowledge and technology in the association area.Known variety carrier and other additive can be used to prepare composition of the present invention.Pharmaceutical composition of the present invention can the standard manner administration to be used for illness to be treated, for example by oral, rectal administration or administered parenterally.
For these purposes, compound of the present invention can be made such as following form by method as known in the art: tablet, capsule, the aqueous solution or oil solution or suspension, (lipid) but emulsion dispersed powders, suppository, ointment, breast frost, drops and the aseptic injection aqueous solution or oil solution or suspension.
Suitable pharmaceutical composition of the present invention is to be suitable for the oral pharmaceutical composition of unit dosage form, as contains tablet or the capsule of about 1mg to about 1g The compounds of this invention.
On the other hand, pharmaceutical composition of the present invention is the pharmaceutical composition that is suitable for intravenously, subcutaneous or intramuscularly.For example the patient can accept the The compounds of this invention of about 1 μ g/kg to about 1g/kg intravenously, subcutaneous or intramuscular dosage.Can use intravenously, subcutaneous and intramuscular dosage by the mode of injecting.Selectively, can use intravenous dosages by continuous infusion in for some time.
Selectively, the patient accepts to approximate greatly the day oral dosage of parenteral dosage every day, and use composition 1-4 every day.
Following table is illustrated in treats among the mankind or the inclusion compound of prophylactic applications or the representative drugs formulation of its pharmacy acceptable salt:
| Tablet 1 | The mg/ |
| Compound | |
| 100 | |
| Lactose Ph.Eur. | 179 |
| Cross-linked carboxymethyl cellulose sodium | 12.0 |
| Polyvinylpyrrolidone | 6 |
| Magnesium Stearate | 3.0 |
| Tablet 2 | The mg/ |
| Compound | |
| 50 | |
| Lactose Ph.Eur. | 229 |
| Cross-linked carboxymethyl cellulose sodium | 12.0 |
| Polyvinylpyrrolidone | 6 |
| Magnesium Stearate | 3.0 |
| Tablet 3 | The mg/ sheet |
| Compound | 1.0 |
| Lactose Ph.Eur. | 92 |
| Cross-linked carboxymethyl cellulose sodium | 4.0 |
| Polyvinylpyrrolidone | 2.0 |
| Magnesium Stearate | 1.0 |
| Capsule | The mg/ capsule |
| Compound | 10 |
| Lactose Ph.Eur. | 389 |
| Cross-linked | 100 |
| Magnesium Stearate | 1.0 |
| Injection I | (50mg/ml) |
| Compound | 0.5％w/v |
| Isotonic aqueous solution | To 100% |
The pharmaceutical composition of the compound of the compound that comprises general formula (I), particularly general formula (VI) can be used for the treatment of the disease, particularly cancer of being regulated by the Wnt signal pathway, more specifically is colorectal carcinoma.
In another aspect of this invention, disclose a kind of method that is used to suppress experimenter's growth of tumour cell, described method comprises compound of the present invention from significant quantity to thin tumour cell that use safety and.Comprise this compound compositions and can also be used to suppress tumour cell.Therefore, this method can be used for the treatment of the cancer of mammalian subject.It can be advantageously used in the treatment colorectal carcinoma.
In another aspect of this invention, disclose a kind of method that is used for the treatment of the disease of being regulated by the Wnt signal pathway, wherein said method comprises the compound of using the compound with general formula (I), particularly general formula (VI) of safety and significant quantity to the patient.The pharmaceutical composition that comprises compound of the present invention also can be used for this purpose.In this, find to have the compound of general formula (I) in the present invention, particularly the compound of general formula (VI) or the pharmaceutical composition that comprises it can be used for the treatment of the disease of being regulated by TCF4-β catenin-CBP complex body, and described complex body is considered to be responsible for causing the overexpression of the cancer cells relevant with the Wnt signal pathway.Therefore, the compounds for treating of the compound that another aspect of the present invention provides a kind of use to have general formula (I), particularly general formula (VI) is by the method for the disease of TCF4-β catenin-CBP complex body adjusting.
And, since treatment for cancer also with induce experimenter's cancer cells generation apoptosis closely related, therefore the invention still further relates to the method for compound cancer cell specific induction of apoptosis of the compound, particularly general formula (VI) of a kind of use general formula (I).
According to the known 5-FU[Fluracil of prior art; 5-fluoro-2,4 (1H, 3H)-pyrimidine dione] can inducing culture mouth cancer cells generation apoptosis (people such as D.Tong, Oral Oncology36,2000236-241).But also known colorectal carcinoma has susceptibility (people such as D.Arango, Cancer Research 61,2001 4910-4915) to 5-FU.Therefore in the present invention, preparation has the combination of compounds of the compound, particularly general formula (VI) of the 5-FU of definite antitumour activity and formula of the present invention (I), and tests at SW480 clone.Found that 5-FU and The compounds of this invention, particularly growth has significant effect as the SW480 cell to the TCF4 combination of compounds to anticancer.
Therefore, another aspect of the present invention provides a kind of treatment method for cancer, described method comprises the compound of the compound with general formula (I), particularly general formula (VI) of using the claim 1 of safety and significant quantity to the experimenter, and other carcinostatic agent such as 5-Fu.
Shown that compound of the present invention suppresses the expression of survivin.People such as Blanc-Brude, Nat.Medicine 8:987 (2002) have shown that survivin is the crucial conditioning agent of smooth muscle cell apoptosis, and it plays an important role in the pathologic tube wall is reinvented.Therefore, the present invention provides the method for a kind of treatment or the prevention restenosis relevant with angioplasty on the other hand, and described method comprises the reverse turn mimetics of the present invention of using safety and significant quantity to the experimenter that these needs are arranged.In one embodiment, the present invention treats restenosis, uses the alleviating of seriousness, scope or degree etc. that reverse turn mimetics of the present invention is realized restenosis promptly for the experimenter suffer from restenosis.In another embodiment, prevention of restenosis of the present invention uses the alleviating of expection seriousness, scope or degree etc. that reverse turn mimetics of the present invention is realized restenosis promptly for new or extra restenosis can take place in expection experimenter.Optional described experimenter is a mammalian subject.
Shown that compound of the present invention suppresses the TCF/B-catenin and transcribes.People such as Rodova, J.Biol.Chem.277:29577 (2002) have shown that the PKD-1 promotor is the target body of B-catenin/TCF approach.Therefore, the present invention provides the method for a kind of treatment or prevention POLYCYSTIC KIDNEY DISEASE on the other hand, and described method comprises the reverse turn mimetics of the present invention of using safety and significant quantity to the experimenter that these needs are arranged.In one embodiment, the present invention treats POLYCYSTIC KIDNEY DISEASE, uses the alleviating of seriousness, scope or degree etc. that reverse turn mimetics of the present invention is realized POLYCYSTIC KIDNEY DISEASE promptly for the experimenter suffer from POLYCYSTIC KIDNEY DISEASE.In another embodiment, the present invention prevents POLYCYSTIC KIDNEY DISEASE, uses the alleviating of expection seriousness, scope or degree etc. that reverse turn mimetics of the present invention is realized POLYCYSTIC KIDNEY DISEASE promptly for new or extra POLYCYSTIC KIDNEY DISEASE can take place in expection experimenter.Optional described experimenter is a mammalian subject.
Shown that compound of the present invention suppresses the expression of Wnt signal effect.People such as Hanai, JCell Bio.158:529 (2002) have shown that a kind of known anti-angiogenesis blood vessel endothelium chalone (endostatin) suppresses the effect of Wnt signal.Therefore, the present invention provides a kind of treatment or prevention abnormal vascular to generate the method for disease on the other hand, and described method comprises the reverse turn mimetics of the present invention of using safety and significant quantity to the experimenter that these needs are arranged.In one embodiment, the present invention treats abnormal vascular and generates disease, uses reverse turn mimetics of the present invention promptly for the experimenter who suffers from abnormal vascular generation disease and realizes that abnormal vascular generates alleviating of severity of disease, scope or degree etc.In another embodiment, the present invention prevents abnormal vascular to generate disease, experimenter that new or extra abnormal vascular generates disease can be taken place promptly for expection and uses reverse turn mimetics of the present invention and realize that abnormal vascular generates the alleviating of expection seriousness, scope or degree etc. of disease.Optional described experimenter is a mammalian subject.
Shown that bonded of the present invention suppresses the expression of Wnt signal effect.People such as Sen, P.N.A.S. (USA) 97:2791 (2000) have shown that Wnt and Fz that the Mammals that suffers from rheumatoid arthritis shows in the RA synovial tissue express increase.Therefore, the present invention provides the method for a kind of treatment or prevention rheumatoid arthritis disease on the other hand, and described method comprises the reverse turn mimetics of the present invention of using safety and significant quantity to the experimenter that these needs are arranged.In one embodiment, the present invention treats the rheumatoid arthritis disease, uses reverse turn mimetics of the present invention promptly for the experimenter who suffers from the rheumatoid arthritis disease and realizes alleviating of rheumatoid arthritis severity of disease, scope or degree etc.In another embodiment, the present invention prevents the rheumatoid arthritis disease, can become the experimenter of new or extra rheumatoid arthritis disease to use the alleviating of expection seriousness, scope or degree etc. that reverse turn mimetics of the present invention is realized the rheumatoid arthritis disease promptly for expection.Optional described experimenter is a mammalian subject.
Shown that compound of the present invention suppresses the expression of Wnt signal effect.People such as Uthoff, Int.J.Oncol 19:803 (2001) have shown that difference takes place raises disorderly fz (Wnt approach molecule) in ulcerative colitis (patient compares with regional ileitis).Therefore, the present invention provides the method for a kind of treatment or prevention of ulcerative colitis on the other hand, and described method comprises the reverse turn mimetics of the present invention of using safety and significant quantity to the experimenter that these needs are arranged.In one embodiment, the present invention treats ulcerative colitis, uses the alleviating of seriousness, scope or degree etc. that reverse turn mimetics of the present invention is realized ulcerative colitis promptly for the experimenter suffer from ulcerative colitis.In another embodiment, prevention of ulcerative colitis of the present invention uses the alleviating of expection seriousness, scope or degree etc. that reverse turn mimetics of the present invention is realized ulcerative colitis promptly for new or extra ulcerative colitis can take place in expection experimenter.Optional described experimenter is a mammalian subject.
Preferred forms of the present invention
Following non-limiting example illustration compound of the present invention, composition and methods for using them.
Embodiment
Preparation embodiment 1:(N-Fmoc-N '-R
3-diazanyl)-preparation of acetate
(1) preparation of N-Fmoc-N '-methyl hydrazine
Be equipped with a glass stopper and a calcium pipe for 2L, two neck, round-bottomed flask.Be added in methyl hydrazine sulfate (20g, 139mmol) solution and the DiBoc (33g, solution 153mmol) that are added among the THF among the THF (300mL).In 2 hours, drip saturated sodium bicarbonate aqueous solution (500mL) and vigorous stirring by addition funnel.After 6 hours, slowly be added in Fmoc-Cl (39g, solution 153mmol) among the THF.The suspension of gained was stirred 6 hours down in 0 ℃.With EA (500mL) extraction mixture, and keep organic layer.With dried over sodium sulfate solution and vacuum-evaporation.The not purified next step of proceeding.
Be equipped with a glass stopper and a calcium pipe for 1L, two neck, round-bottomed flask.Be added in the solution of the reaction mixture among the MeOH (300mL), slowly add dense HCl (30mL, magnetic agitation 12N) and in ice-water bath, and stir and spend the night by addition funnel.With EA (1000mL) extraction mixture, and keep organic layer.Use dried over sodium sulfate solution, and vacuum-evaporation.With normal hexane and EA the residue crystallized purifying is obtained product (32.2g, 83%).
1HNMR(DMSO-D
6)δ7.90-7.88(d，J＝6Hz，2H，)，δ7.73-7.70(d，J＝9Hz，2H，)，7.44-7.31(m，4H)，4.52-4.50(d，J＝6Hz，2H)，4.31-4.26(t，J＝6Hz，1H)，2.69(s，1H)
The preparation of (2) (N-Fmoc-N '-methyl-diazanyl)-tert.-butyl acetate
Give 1L, two neck, round-bottomed flask be equipped with a glass stopper and with the reflux exchanger of a calcium pipe coupling.Be added in N-Fmoc-N '-methyl-hydrazine (20g, solution 75mmol) in the toluene (300mL).Slowly be added in tert.-butyl bromide acetic ester (22g, solution 111mmol) in the toluene (50mL).Slowly add Cs
2CO
3(49g, 149mmol).Slow adding NaI (11g, 74mmol), and vigorous stirring.Reaction mixture was stirred 1 day down in reflux temperature.Mixture is filtered, and (500mL) extract organic layer with ethyl acetate [EA].Use dried over sodium sulfate solution, and vacuum-evaporation.Use hexane: EA=2: 1 solution is made the chromatogram purifying with product and is obtained product (19.8g, 70%).
1H-NMR(CDCl
3-d)δ7.78-7.75(d，J＝9Hz，2H，)，δ7.61-7.59(d，J＝6Hz，2H，)，7.43-7.26(m，4H)，4.42-4.40(d，J＝6Hz，2H)，4.23(b，1H)，3.57(s，2H)，2.78(s，3H)，1.50(s，9H)
The preparation of (3) (N-Fmoc-N '-methyl-diazanyl)-acetate
Be equipped with the reflux exchanger of a glass stopper and and calcium pipe coupling for 1L, two neck, round-bottomed flask.Add (N-Fmoc-N '-methyl-diazanyl)-tert.-butyl acetate (20g, 52mmol).Slowly add HCl solution (150mL, the solution of 4M in two alkane) and vigorous stirring in ice-water bath.To react mixed thing stirred 1 day down in RT.Reduce pressure solution concentrated fully in 40 ℃.Add saturated NaHCO
3The aqueous solution (100mL), and with diethyl ether (100mL) washing water layer.Slowly drip dense HCl (pH2-3) down at 0 ℃.The extraction mixture, and the reservation organic layer (500mL, MC).With dried over sodium sulfate solution and vacuum-evaporation.With normal hexane and ethyl acetate the resistates recrystallization purifying is obtained product (12g, 72%).
1H-NMR(DMSO-d
6)δ12.38(s，1H)，8.56(b，1H)，7.89-7.86(d，J＝9Hz，2H，)，δ7.70-7.67(d，J＝9Hz，2H，)，7.43-7.29(m，4H)，4.29-4.27(d，J＝6Hz，2H)，4.25-4.20(t，J＝6Hz，1H)，3.47(s，2H)，2.56(s，3H)
Preparation embodiment 2:(N-Moc-N '-R
7-diazanyl)-preparation of acetate
The preparation of (1) (N '-methoxycarbonyl-diazanyl)-ethyl acetate
With the carbazic acid methyl esters (50g 0.55mol) is dissolved in DMF (300ml), then with ethyl bromoacetate (68ml, 0.555mol), (77g 0.555mol) is added to reaction vessel to salt of wormwood.Mixture heating up to 50 ℃ is continued 5 hours.After reaction is finished, mixture is filtered, with the EtOAc dilution, and with salt water washing (3 times).With column purification crude product (eluent: Hex/EtOAc=4/1).
Pdt:72g (water white oil)
(2) [N-R
7-N '-methoxycarbonyl-diazanyl]-ethyl acetate
With ethyl ester (10g, 0.05mol), salt of wormwood (6.9g, 0.05mol) and R
3(14.1g 0.06mol) is dissolved in DMF (200ml) to-bromide, and mixture heating up to 50 ℃ is continued 5 hours.After reaction is finished, mixture is filtered, with the EA dilution, and with salt water washing (3 times).With chromatography (eluent: Hex/EtOAc=4/1) purifying crude product.
(3) [N-R
7-N '-methoxycarbonyl-diazanyl]-acetate
With the alkylation ethyl ester (9.5g, 0.03mol) be dissolved in THF/ water (1/1, ml), and add down 2N NaOH (28.3ml) solution at 0 ℃.Mixture was stirred 2 hours down in RT.After detecting less than starting ester with UV, use the EA diluting soln, separate then.With 1N HCl water layer is acidified to pH 3-4, and with DCM extract compounds (3 times).Use MgSO
4The dry organic layer that merges, and evaporation obtains a kind of yellow solid.
Embodiment 1
(1) N
β-Moc-N
αThe preparation of-benzyl-diazanyl glycine
Prepare this compound according to literature method.(people such as Cheguillaume, Synlett 2000,3, and 331)
(2) 1-methoxycarbonyl-2,8-dibenzyl-6-methyl-4,7-dioxo-six hydrogen-pyrazine be the preparation of [2,1-c] [1,2,4] triazine also
With the bromoacetal resin (60mg, 0.98mmol/g) and the benzyl amine aqueous solution in DMSO (2.5ml, 2M) be placed on the band nut bottle in.Use rotary oven [RobbinsScientific] with reaction mixture vibration 12 hours down at 60 ℃.Filter and collect resin,, wash with DCM then with the DMF washing.
Will be at Fmoc-L-Ala (4 equivalent), the HATU[PerSeptive Biosystems among the NMP (Advanced ChemTech)] solution of (4 equivalent) and DIEA (4 equivalent) is added to resin.Reaction mixture, is being filtered and collecting resin after 4 hours in vibration under the room temperature, and, washing with DMF then with DMF, DCM washing.
Be added in 20% piperidines among the DMF in the resin.At room temperature the reaction mixture vibration after 8 minutes, is filtered and collected resin, and, wash with DMF then with DMF, DCM washing.
N that will be in DMF
β-Moc-N
α-benzyl-diazanyl glycine (4 equivalent), HOBT[Advanced Chem Tech] solution of (4 equivalent) and DIC (4 equivalent) is added to the resin of above preparation.At room temperature the reaction mixture vibration after 3 hours, is filtered and collected resin, and, wash with MeOH then with DMF, DCM washing.Vacuum-drying resin at room temperature.
With formic acid (2.5ml) resin was handled under room temperature 18 hours.Remove by filter after the resin, concentrating under reduced pressure filtrate obtains product, is oil.
1H-NMR(400MHz，CDCl
3)δppm；1.51(d，3H)，2.99(m，1H)，3.39(d，1H)，3.69(m，1H)，3.75(m，1H)，3.82(s，3H)，4.02(d，1H)，4.24(d，1H)，4.39(d，1H)，4.75(d，1H)，5.14(q，1H)，5.58(dd，1H)，7.10-7.38(m，10H)。
Embodiment 2
(1) preparation of N '-Fmoc-N-methyl-diazanyl carbonyl chloride
Will be at 15ml CH
2Cl
2With the saturated NaHCO of 15ml
3N-methyl hydrazine formic acid 9H-fluorenes in the aqueous solution-(107mg, ice-cold biphasic mixture 0.4mmol) stirs 9-base methyl esters fast, and disposable toluene (1.03ml, 2mmol) the 1.93M phosgene in of being added in.Reaction mixture was stirred 30 minutes, collect organic phase, use CH
2Cl
2Aqueous phase extracted.Use MgSO
4The dry organic phase that merges is filtered and concentrating under reduced pressure obtains 128mg (97%) urea chloride, is a kind of foam solid.[note: the phosgene steam is highly toxic.In ventilating hood, use it].This product is used for following solid phase synthesis without being further purified.
(2) 2,5-dimethyl-7-benzyl-3, the preparation of 6-dioxo-six hydrogen-[1,2,4] triazolo [4,5-a] pyrazine-1-formic acid benzyl acid amides
With the bromoacetal resin (30mg, 0.98mmol/g) and the benzyl amine aqueous solution in DMSO (1.5ml, 2M) be placed on the band nut bottle in.Use rotary oven [RobbinsScientific] with reaction mixture vibration 12 hours down at 60 ℃.Filter and collect resin,, wash with DCM then with the DMF washing.
Will be at Fmoc-L-Ala (3 equivalent), the HATU[PerSeptive Biosystems among the NMP (Advanced ChemTech)] solution of (3 equivalent) and DIEA (3 equivalent) is added to resin.Reaction mixture, is being filtered and collecting resin after 4 hours in vibration under the room temperature, and, washing with DMF then with DMF, DCM washing.
Be added in 20% piperidines among the DMF in the resin.At room temperature the reaction mixture vibration after 8 minutes, is filtered and collected resin, and, wash with DMF then with DMF, DCM washing.
The N '-Fmoc-N-methyl-diazanyl carbonyl chloride (5 equivalent) that will the above step (1) in DCM obtains, the solution of DIEA (5 equivalent) are added to the resin of above preparation.At room temperature the reaction mixture vibration after 4 hours, is filtered and collected resin, and wash with DMF, DCM and DMF.
Be added in 20% piperidines (is 10ml for the 1g resin) among the DMF in the resin.At room temperature the reaction mixture vibration after 8 minutes, is filtered and collected resin, and, wash with DMF then with DMF, DCM washing.
The mixture that is used in isocyanic acid benzyl ester (4 equivalent) among the DCM and DIEA (4 equivalent) under the room temperature was with plastic resin treatment 4 hours.Then, filter and collect resin, and, wash with MeOH then with DMF, DCM washing.Under the room temperature with resin vacuum-drying.
Under the room temperature with formic acid with plastic resin treatment 14 hours.After removing by filter resin, filtrate decompression concentrated obtain product, be a kind of oil.
1H-NMR(400MHz，CDCl
3)δppm；1.48(d，3H)，2.98(s，3H)，3.18(m，1H)，3.46(m，1H)，4.37-4.74(m，5H)，5.66(dd，1H)，6.18(m，1H)，7.10-7.40(m，10H)。
Embodiment 3
2,5,7-trimethylammonium-3,6-dioxo-six hydrogen-[1,2,4] triazolo [4,5-a] pyrazine-1-formic acid benzyl acid amides
Prepare title compound according to the method identical with embodiment 2.
1H-NMR(400MHz，CDCl
3)δppm；1.48(d，3H)，2.99(s，3H)，3.03(s，3H)，3.38(m，1H)，3.53(dd，1H)，4.36(dd，1H)，4.52(q，1H)，4.59(dd，1H)，5.72(dd，1H)，6.19(br.t，1H)，7.10-7.38(m，5H)。
Embodiment 4
2-methyl-5-(para hydroxybenzene ylmethyl)-7-naphthyl methyl-3, the preparation of 6-dioxo-six hydrogen-[1,2,4] triazolo [4,5-a] pyrazine-1-formic acid benzyl acid amides
With the bromoacetal resin (30mg, 0.98mmol/g) and the naphthyl methyl amine aqueous solution in DMSO (1.5ml, 2M) be placed on the band nut bottle in.Use rotary oven [Robbins Scientific] with reaction mixture vibration 12 hours down at 60 ℃.Filter and collect resin,, wash with DCM then with the DMF washing.
Will be at Fmoc-Tyr (OBut)-OH (3 equivalent), the HATU[PerSeptive Biosystems among the NMP (Advanced ChemTech)] solution of (3 equivalent) and DIEA (3 equivalent) is added to resin.Reaction mixture, is being filtered and collecting resin after 4 hours in vibration under the room temperature, and, washing with DMF then with DMF, DCM washing.
Be added in 20% piperidines among the DMF in the resin.At room temperature the reaction mixture vibration after 8 minutes, is filtered and collected resin, and, wash with DMF then with DMF, DCM washing.
N '-Fmoc-N-methyl-diazanyl carbonyl chloride (5 equivalent) that will be in DCM, the solution of DIEA (5 equivalent) are added to the resin of above preparation.At room temperature the reaction mixture vibration after 4 hours, is filtered and collected resin, and wash with DMF, DCM and DMF.
Be added in 20% piperidines (is 10ml for the 1g resin) among the DMF in the resin.Under the room temperature reaction mixture vibration after 8 minutes, is filtered and collected resin,, wash with DMF then with DMF, DCM washing resin.
The mixture that is used in isocyanic acid benzyl ester (4 equivalent) among the DCM and DIEA (4 equivalent) under the room temperature was with plastic resin treatment 4 hours.Then, filter and collect resin, and, wash with MeOH then with DMF, DCM washing.Under the room temperature with resin vacuum-drying.
Under the room temperature with formic acid with plastic resin treatment 14 hours.After removing by filter resin, filtrate decompression concentrated obtain product, be a kind of oil.
1H-NMR(400MHz，CDCl
3)δppm；2.80-2.98(m，5H)，3.21-3.37(m，2H)，4.22-4.52(m，2H)，4.59(t，1H)，4.71(d，1H)，5.02(dd，1H)，5.35(d，1H)，5.51(d，1H)，6.66(t，2H)，6.94(dd，2H)，7.21-8.21(m，12H).
Embodiment 5
2-methyl-6-(para hydroxybenzene ylmethyl)-8-naphthyl-4,7-dioxo-six hydrogen-pyrazine be the preparation of [2,1-c] [1,2,4] triazine-1-formic acid benzyl acid amides also
With the bromoacetal resin (60mg, 0.98mmol/g) and the ALPHA-NAPHTHYL AMINE solution in DMSO (2.5ml, 2M) be placed on the band nut bottle in.Use rotary oven [RobbinsScientific] with reaction mixture vibration 12 hours down at 60 ℃.Filter and collect resin,, wash with DCM then with the DMF washing.
Will be at Fmoc-Tyr (OBut)-OH (4 equivalent), the HATU[PerSeptive Biosystems among the NMP (Advanced ChemTech)] solution of (4 equivalent) and DIEA (4 equivalent) is added to resin.Reaction mixture, is being filtered and collecting resin after 4 hours in vibration under the room temperature, and, washing with DMF then with DMF, DCM washing.
Be added in 20% piperidines among the DMF in the resin.At room temperature the reaction mixture vibration after 8 minutes, is filtered and collected resin, and, wash with DMF then with DMF, DCM washing.
N β-Fmoc-N α-benzyl-diazanyl glycine (4 equivalent), HOBT[Advanced ChemTech that will be in DMF] solution of (4 equivalent) and DIC (4 equivalent) is added to the resin of above preparation.Under the room temperature reaction mixture vibration after 3 hours, is filtered and collected resin, and, wash with DCM then with the DMF washing.Be added in 20% piperidines (is 10ml for the 1g resin) among the DMF in the resin.Under the room temperature reaction mixture vibration after 8 minutes, is filtered and collected resin, and, wash with DMF then with DMF, DCM washing.
The mixture that is used in isocyanic acid benzyl ester (4 equivalent) among the DCM and DIEA (4 equivalent) under the room temperature was with plastic resin treatment 4 hours.Then, filter and collect resin, and, wash with MeOH then with DMF, DCM washing.Under the room temperature with after the resin vacuum-drying, under the room temperature with formic acid (2.5ml) with plastic resin treatment 18 hours.Remove by filter resin, and concentrating under reduced pressure filtrate obtains product, be a kind of oil.
1H-NMR(400MHz，CDCl
3)δppm：2.73(s，3H)，3.13(d，1H)，3.21-3.38(m，3H)，3.55(d，1H)，3.75(t，1H)，4.22(dd，1H)，4.36(dd，1H)，4.79(d，1H)，5.22(t，1H)，5.47(m，2H)，6.68(d，2H)，6.99(d，2H)，7.21-8.21(m，12H)；
MS(m/z，ESI)564.1(MH
+)586.3(MNa
+).
Embodiment 6
About measuring IC at the SW480 cell
50Bioanalysis and the cell toxicity test of pair cell system carry out by the following method:
Test compound preparation in embodiment 4.
Reporter gene is analyzed
Use Superfect
TMTransfection reagent (Qiagen, 301307) transfection SW480 cell.Simply with the cell tryptase protease digestion, and be placed on 6 hole flat boards (5 * 10 preceding 1 day of transfection
5Cells/well), thus they are converged at transfection 50-80% on the same day.
Do not contain the DNA of dilution 4 micrograms (TOPFlash) and 1 microgram (pRL-null) in the substratum of serum at 150 μ l, and add 30 μ l Superfect
TMTransfection reagent.At room temperature the DNA-Superfect mixture was cultivated 15 minutes, 1ml 10%FBS DMEM is added to carries out other 3 hours cultivation in this complex body then.When forming complex body, with not containing antibiotic PBS with the cell washing secondary.
With DNA-Superfect
TMThe transfection reagent complex body is applied to cell, then at 37 ℃ and 5%CO
2The middle cultivation 3 hours.After the cultivation, add the recovery media that contains 10%FBS, so that final volume is 1.18ml.After carrying out cultivating in 3 hours, harvested cell, and inoculate 96 hole flat boards (3 * 10
4Cells/well).At 37 ℃ and 5%CO
2After the middle overnight incubation, cell was handled 24 hours with test compound.At last, (Promega E1960) checks activity by the luciferase analysis.
The above compound of Fig. 1 illustration is to the IC of SW480 cell
50Measurement result.
Sulphur rhodamine B (SRB) is analyzed
By of the growth-inhibiting effect of the above compound of sulphur rhodamine B assay determination to following cell.To place every hole of 96 hole flat boards at the SW480 cell in the 100 μ l substratum, and make its attached wall 24 hours.Compound is added to the ultimate density to obtain expecting in the hole, and flat board was cultivated 48 hours down in 37 ℃.Be added to every hole by lentamente that 100 μ l are cold (4 ℃) 10% trichoroacetic acid(TCA) then, cultivated 1 hour and fixed cell down at 4 ℃ subsequently.With deionized water flat board is washed 5 times, and make it air-dry.Then by 100 μ lSRB solution (0.4%SRB (w/v) in 1% acetate (v/v)) being added in the hole 15 minutes and with cell dyeing.After the dyeing, with 1% acetate wash fast dull and stereotyped 5 times removing any unconjugated dyestuff, and it is air-dry.With 10mmol/L Tris alkali (pH 10.5) the bonded dyestuff is dissolved, then to dull and stereotyped reading.On plate reading machine, under the wavelength of 515nm, read optical density(OD) (OD) with Molecular Device.Growth-inhibiting is expressed as relative viability (% contrast), and calculates GI by concentration-response curve after the log/ probability transforms
50
The vitro cytotoxicity of the compound that [table 6] embodiment 4 obtains (SRB) is analyzed
| The source | Cell | Embodiment 4 | Cis-platinum | 5-FU |
| Colon | T84 | 1.134 | ＞10 | 1.816 |
| LOVO | 0.532 | ＞10 | 1.029 | |
| HT29 | 1.694 | ＞10 | 5.334 | |
| DLD-1 | 1.775 | ＞10 | ＞10 | |
| COLO205 | 1.136 | ＞10 | 1.130 | |
| CACO-2 | 1.201 | ＞10 | 0.451 | |
| SW480-Kribb | 1.137 | ＞10 | ＞10 | |
| SW480-CWP | 0.980 | 4.502 | ＞10 | |
| SW620 | 1.426 | ＞10 | 5.570 | |
| KM12 | 1.451 | ＞10 | 2.729 | |
| HCT15 | 2.042 | ＞10 | 1.179 | |
| HCT116 | 0.96 | ＞10 | 1.039 | |
| HCC2998 | 1.047 | ＞10 | 5.486 | |
| 786-0 | 1.417 | 3.347 | 0.584 | |
| Leukemia | HL60 | 1.243 | ＞10 | 7.010 |
| RPMI8226 | 1.1.177 | ＞10 | ＞10 | |
| K562/VIN | 1.640 | ＞10 | 7.071 | |
| K562/ADR | 7.682 | ＞10 | ＞10 | |
| K562 | 1.247 | ＞10 | 6.133 | |
| Prostate gland | PC3 | 1.207 | ＞10 | ＞10 |
| HT1080 | 1.469 | ＞10 | 0.798 | |
| Lung | A549 | 1.386 | ＞10 | 1.007 |
| NCI H460 | 1.498 | ＞10 | 1.397 | |
| NCI H23 | 1.296 | 5.176 | 2.254 | |
| Kidney | 293 | 0.731 | 6.641 | 2.015 |
| CAKI-1 | 0.467 | ＞10 | 0.925 | |
| ACHN | 1.263 | 5.019 | 5.062 | |
| Melanoma | RPMI7951 | 0.936 | 5.010 | 0.920 |
| M14 | 2.289 | 3.447 | 1.225 | |
| HMV-II | 4.834 | 3.190 | 0.695 | |
| HMV-I | 1.153 | 5.478 | 2.110 | |
| G361 | 0.584 | 4.827 | 1.539 | |
| CRL1579 | 1.830 | 0.699 | ＞10 | |
| A431 | 1.083 | 3.722 | 0.404 | |
| A253 | 1.398 | 2.084 | 2.926 | |
| UACC62 | 0.563 | ＞10 | 1.093 | |
| SK-MEL-28 | 1.291 | ＞10 | ＞10 | |
| SK-MEL-5 | 0.888 | ＞10 | 2.434 | |
| LOX-IMVI | 1.526 | ＞10 | ＞10 | |
| A375 | 1.391 | ＞10 | 1.464 | |
| Mammary gland | MCF7/ADR | 9.487 | 9.907 | ＞10 |
| MCF7 | 7.355 | ＞10 | 1.751 |
Though be appreciated that here and described particular of the present invention for illustrative purpose, can under the situation that does not deviate from design of the present invention and scope, make multiple remodeling.Therefore, the present invention is unrestricted except that appended claim.
Industrial applicibility
Expression, the TCF/B-catenin that the compound of the present invention of the secondary structure in the inflection district of simulation biologically active peptides and proteins can suppress survivin transcribed the expression with the Wnt signal function. Therefore, it is a kind of for suppressing the mammalian subject growth of tumour cell that the present invention can provide, with other antineoplastic therapeutic alliance cancer, treatment or prevent disease generate pharmaceutical composition and/or the method for disease, rheumatoid arthritis disease and ulcerative colitis such as the ISR relevant with angioplasty, POLYCYSTIC KIDNEY DISEASE, abnormal vascular, and a kind of method of identification of organism reactive compound, and library of compounds.
Claims (13)
1. the compound that has following general formula (I):
Wherein A be-(C=O)-, B is-(CHR
4)-, D is-(C=O)-, E is-(ZR
6)-, G is-(XR
7)
n-, W is-Y (C=O)-,-(C=O) NH-,-(SO
2)-or do not exist, Y is oxygen or sulphur, X and Z are CH, n=1; And R
1, R
2, R
4, R
6And R
7Identical or different and be independently selected from amino acid side chain moiety, amino acid side chain derivative, connector and solid carrier.
2. the compound of claim 1, wherein R
1, R
2, R
4, R
6And R
7Be independently selected from: amino C
2-5Alkyl, guanidine radicals C
2-5Alkyl, C
1-4Alkyl guanidine radicals C
2-5Alkyl, two C
1-4Alkyl guanidine radicals-C
2-5Alkyl, amidino groups C
2-5Alkyl, C
1-4Alkyl amidine C
2-5Alkyl, two C
1-4Alkyl amidine C
2-5Alkyl, C
1-3(wherein said substituting group is independently selected from amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to the phenyl of alkoxyl group, phenyl, replacement
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3One or more in alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or the hydroxyl), (wherein the substituting group on the benzyl is independently selected from amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to the benzyl of benzyl, replacement
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-3One or more in alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or the hydroxyl), (wherein said substituting group is independently selected from amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to the naphthyl of naphthyl, replacement
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3One or more in alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or the hydroxyl), (wherein said substituting group is independently selected from amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to two phenyl methyls of two phenyl methyl, replacement
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3One or more in alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or the hydroxyl), (wherein said substituting group is independently selected from amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to the pyridyl of pyridyl, replacement
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3One or more in alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or the hydroxyl), pyridyl C
1-4The pyridyl C of alkyl, replacement
1-4(wherein said pyridine substituting group is independently selected from amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to alkyl
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3One or more in alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or the hydroxyl), pyrimidyl C
1-4The pyrimidyl C of alkyl, replacement
1-4(wherein said pyrimidine substituting group is independently selected from amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to alkyl
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3One or more in alkoxyl group or nitro, carboxyl, cyano group, alkylsulfonyl or the hydroxyl), triazine-2-base-C
1-4The triazine of alkyl, replacement-2-base-C
1-4(wherein said triazine substituting group is independently selected from amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to alkyl
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3One or more in alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or the hydroxyl), imidazoles C
1-4The imidazoles C of alkyl, replacement
1-4(wherein said imidazole substituent is independently selected from amino, amidino groups, guanidine radicals, diazanyl, amino hydrazone group, C to alkyl
1-4Alkylamino, C
1-4Dialkyl amido, halogen, perfluoro C
1-4Alkyl, C
1-4Alkyl, C
1-3One or more in alkoxyl group, nitro, carboxyl, cyano group, alkylsulfonyl or the hydroxyl), imidazolinyl C
1-4Alkyl, N-amidino groups piperazinyl-N-C
0-4Alkyl, hydroxyl C
2-5Alkyl, C
1-5Alkylamino C
2-5Alkyl, hydroxyl C
2-5Alkyl, C
1-5Alkylamino C
2-5Alkyl, C
1-5Dialkyl amido C
2-5Alkyl, N-amidinopiperidinyl C
1-4Alkyl and 4-aminocyclohexyl C
0-2Alkyl.
3. the compound of claim 2, wherein R
1, R
2, R
4, R
6Or R
7Be connected on solid carrier or the solid carrier derivative.
4. pharmaceutical composition comprises among the claim 1-3 each compound and pharmaceutically acceptable carrier.
5. the compound of each of claim 1-3 is used for suppressing the purposes of the medicine of mammalian subject growth of tumour cell in preparation.
6. the purposes of claim 5, wherein said tumour cell is a colorectal cell.
7. the compound of each of claim 1-3 and other antitumour drug are combined in the purposes in the medicine for preparing the treatment cancer.
8. the purposes of claim 7, wherein said antitumour drug is selected from 5-FU, taxol, cis-platinum, ametycin, Tegafur, Raltitrexed, capecitabine and irinotecan.
9. the purposes of the compound of each of claim 1-3 in the medicine of preparation treatment or the prevention restenosis relevant with angioplasty.
10. the purposes of the compound of each of claim 1-3 in the medicine of preparation treatment or prevention POLYCYSTIC KIDNEY DISEASE.
11. the purposes of the compound of each of claim 1-3 in the medicine of preparation treatment or prevention abnormal vascular generation disease.
12. the purposes of the compound of each of claim 1-3 in the medicine of preparation treatment or prevention rheumatoid arthritis disease.
13. the purposes of the compound of each of claim 1-3 in the medicine of preparation treatment or prevention of ulcerative colitis.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US97647001A | 2001-10-12 | 2001-10-12 | |
| US09/976,470 | 2001-10-12 | ||
| US10/087,443 | 2002-03-01 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB028225678A Division CN100475816C (en) | 2001-10-12 | 2002-10-11 | Reverse-turn mimetics and method relating thereto |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1872857A true CN1872857A (en) | 2006-12-06 |
Family
ID=37483476
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 200610093786 Pending CN1872856A (en) | 2001-10-12 | 2002-10-11 | Reverse-turn mimetics and method relating thereto |
| CN 200610093787 Pending CN1872857A (en) | 2001-10-12 | 2002-10-11 | Reverse-turn mimetics and method relating thereto |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 200610093786 Pending CN1872856A (en) | 2001-10-12 | 2002-10-11 | Reverse-turn mimetics and method relating thereto |
Country Status (1)
| Country | Link |
|---|---|
| CN (2) | CN1872856A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101270142B (en) * | 2008-04-17 | 2011-09-21 | 大连大学 | Method for preparing oil tea saponin |
| CN105017034B (en) * | 2014-04-17 | 2019-02-15 | 中国科学院上海药物研究所 | Alkamine compound, preparation method, the medical composition and its use comprising such compound |
-
2002
- 2002-10-11 CN CN 200610093786 patent/CN1872856A/en active Pending
- 2002-10-11 CN CN 200610093787 patent/CN1872857A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CN1872856A (en) | 2006-12-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1585770A (en) | Reverse-turn mimetics and method relating thereto | |
| US10906907B2 (en) | Tert-butyl (s)-(1-(5-fluoro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)propyl)carbamate precursor of a quinazolinone inhibitor of human phosphatidylinositol 3-kinase delta and a process for preparing thereof | |
| CN1156477C (en) | Alkylamino substituted bicyclic nitrogen heterocycles as inhibitors of P38 protein kinase | |
| CN1942472A (en) | Reverse-turn mimetics and method relating thereto | |
| CN1137123C (en) | Azolo triazizes and pyrimidines | |
| US20100069333A1 (en) | Alpha-helix mimetics and method relating to the treatment of cancer stem cells | |
| Zak et al. | Discovery and optimization of C-2 methyl imidazopyrrolopyridines as potent and orally bioavailable JAK1 inhibitors with selectivity over JAK2 | |
| CN1798746A (en) | Reverse-turn mimetics and method relating thereto | |
| JP2020526543A (en) | Inhibitor of leucine-rich repeat kinase 2 | |
| CN1440403A (en) | Quinazoline ditosylate salt compounds | |
| EA008241B1 (en) | Inhibitors of human phosphatidyl-inositol 3-kinase delta | |
| CN1882591A (en) | 5,7-diaminopyrazolo '4,3-d!pyrimidines with pde-5 inhibiting activity | |
| CN1681818A (en) | Azaindole kinase inhibitors | |
| CN1599729A (en) | HIV protease inhibitors, compositions containing the same, their pharmaceutical uses and materials for their synthesis | |
| CN1820009A (en) | Pyrrolo[3,4-c]pyrazole derivatives active as kinase inhibitors | |
| CN1409711A (en) | Fused naphthalene dinitrogen compound useful as HIV reverse transcriptase inhibitors | |
| JP5759999B2 (en) | N-((1R, 2S, 5R) -5- (TERT-butylamino) -2-((S) -3- (7-TERT-butylpyrazolo [1,5-a] [1,3,5] triazine -4-ylamino) -2-oxopyrrolidin-1-yl) cyclohexyl) acetamide, dual modulator of chemokine receptor activity, crystal form and process | |
| JP2018504441A (en) | Novel fluorinated derivatives as EGFR inhibitors useful in the treatment of cancer | |
| CN1694705A (en) | Novel pyrazolopyrimidines as cyclin dependent kinase inhibitors | |
| CN1229335C (en) | Nervinolin derivatives | |
| CN1966506A (en) | Pyrromonazole pyrimidinone derivatives, method of producing them and use thereof | |
| JP2020506966A (en) | Compound | |
| CN1872857A (en) | Reverse-turn mimetics and method relating thereto | |
| US10039769B2 (en) | Substituted triazolobenzodiazepines | |
| CN1160075C (en) | Use of heterocyclic amide compound for producing IgE antibody production inhibitor |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |