FR2034481A1 - (2,3-epoxypropyl)-phosphonic acid derivs with - antibacterial activity - Google Patents
(2,3-epoxypropyl)-phosphonic acid derivs with - antibacterial activityInfo
- Publication number
- FR2034481A1 FR2034481A1 FR7002085A FR7002085A FR2034481A1 FR 2034481 A1 FR2034481 A1 FR 2034481A1 FR 7002085 A FR7002085 A FR 7002085A FR 7002085 A FR7002085 A FR 7002085A FR 2034481 A1 FR2034481 A1 FR 2034481A1
- Authority
- FR
- France
- Prior art keywords
- antibacterial activity
- epoxypropyl
- phosphonic acid
- acid derivs
- nr1r2
- 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.)
- Withdrawn
Links
- 230000000844 anti-bacterial effect Effects 0.000 title abstract 2
- CYACGDOQOAHSLC-UHFFFAOYSA-N oxiran-2-ylmethylphosphonic acid Chemical compound OP(O)(=O)CC1CO1 CYACGDOQOAHSLC-UHFFFAOYSA-N 0.000 title 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- -1 R1 and R2 are H Chemical group 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/65502—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a three-membered ring
- C07F9/65505—Phosphonic acids containing oxirane groups; esters thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/44—Amides thereof
- C07F9/4461—Amides thereof the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4465—Amides thereof the amide moiety containing a substituent or a structure which is considered as characteristic of aliphatic amines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Mixtures of the (+) - and (-)-isomers of cpds. of formula (I) (where R1 is H or lower alkyl, X is O or S, and Y and Z are -OR, -SR, -NR1 R2, -NR-CHR-COOH, -NR- OR, -NR-NR1R2, -NR-N=CR1R2, -NR-C(=NR)-NR1 R2, -NH-CX-XR, -NH-CX- NR1R2, -N=C=X, -O-COR, -N3 or halogen, Y and Z not simultaneously being alkoxy; R is H or hydrocarbyl, R1 and R2 are H, hydrocarbyl, alkoxy or acyl) and salts of those cpds. in which Y and/or Z is -OH or -SH and cyclic derivs. in which Y and Z are linked through the residue of a polyfunctional hydrocarbon cpd. are new and have antibacterial activity. Processes for their manufacture and intermediates in such processes are also claimed.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US79357069A | 1969-01-23 | 1969-01-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
FR2034481A1 true FR2034481A1 (en) | 1970-12-11 |
Family
ID=25160219
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR7002085A Withdrawn FR2034481A1 (en) | 1969-01-23 | 1970-01-21 | (2,3-epoxypropyl)-phosphonic acid derivs with - antibacterial activity |
Country Status (4)
Country | Link |
---|---|
BR (1) | BR6914868D0 (en) |
DE (1) | DE2002807A1 (en) |
FR (1) | FR2034481A1 (en) |
NL (1) | NL7000226A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2833266A1 (en) * | 2001-12-11 | 2003-06-13 | Mayoly Spindler Lab | NOVEL PHOSPHONATE DERIVATIVES, PROCESS FOR THEIR PREPARATION, THEIR USE AS MODULATORS OF TGAMMA9 DELTA2 LYMPHOCYTE ACTIVITY |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2270021A1 (en) | 2009-06-18 | 2011-01-05 | Centre National de la Recherche Scientifique | Phosphonates synthons for the synthesis of phosphonates derivatives showing better bioavailability |
-
1969
- 1969-12-08 BR BR21486869A patent/BR6914868D0/en unknown
-
1970
- 1970-01-08 NL NL7000226A patent/NL7000226A/xx unknown
- 1970-01-21 FR FR7002085A patent/FR2034481A1/en not_active Withdrawn
- 1970-01-22 DE DE19702002807 patent/DE2002807A1/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2833266A1 (en) * | 2001-12-11 | 2003-06-13 | Mayoly Spindler Lab | NOVEL PHOSPHONATE DERIVATIVES, PROCESS FOR THEIR PREPARATION, THEIR USE AS MODULATORS OF TGAMMA9 DELTA2 LYMPHOCYTE ACTIVITY |
WO2003050128A1 (en) * | 2001-12-11 | 2003-06-19 | Laboratoire Mayoly Spindler | Phosphonates useful as modulators of t $g(g)9$g(d)2 lymphocyte activity |
JP2005511748A (en) * | 2001-12-11 | 2005-04-28 | ラボラトワール マヨリー スピンドレ | Phosphonates useful as modulators of T-gamma-9-delta-2 lymphocyte activity |
US8017596B2 (en) | 2001-12-11 | 2011-09-13 | Innate Pharma, S.A. | Phosphonates useful as modulators of T-γ-9-δ-2 activity |
Also Published As
Publication number | Publication date |
---|---|
NL7000226A (en) | 1970-07-27 |
BR6914868D0 (en) | 1973-03-20 |
DE2002807A1 (en) | 1970-07-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
ST | Notification of lapse |