JP5052730B2

JP5052730B2 - ステロイド由来抗生物質

ステロイド由来抗生物質 Download PDF

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Publication number: JP5052730B2
Authority: JP; Japan
Prior art keywords: compound; mmol; added; compounds; side chain
Prior art date: 2000-08-15
Legal status : Expired - Fee Related

Application number

JP2002519479A

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English (en)

Japanese (ja)

Other versions

JP2004506645A5 (enExample

JP2004506645A (ja

Inventor

ポールビー．サベッジ

チュンチョンリ

Original Assignee

ブリガムヤングユニバーシティ

Priority date

2000-08-15

Filing date

2001-08-15

Publication date

2012-10-17

2001-08-15 Application filed by ブリガムヤングユニバーシティ filed Critical ブリガムヤングユニバーシティ

2004-03-04 Publication of JP2004506645A publication Critical patent/JP2004506645A/ja

2005-03-17 Publication of JP2004506645A5 publication Critical patent/JP2004506645A5/ja

2012-10-17 Application granted granted Critical

2012-10-17 Publication of JP5052730B2 publication Critical patent/JP5052730B2/ja

2021-08-15 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

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239000003242 anti bacterial agent Substances 0.000 title description 38
229940088710 antibiotic agent Drugs 0.000 title description 33
150000003431 steroids Chemical class 0.000 title description 27
150000001875 compounds Chemical class 0.000 claims description 294
238000000034 method Methods 0.000 claims description 35
-1 amino, carboxy, cyano, methylsulfonylamino Chemical group 0.000 claims description 28
230000035699 permeability Effects 0.000 claims description 16
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical group NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims description 14
235000001014 amino acid Nutrition 0.000 claims description 13
229940024606 amino acid Drugs 0.000 claims description 13
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
125000006239 protecting group Chemical group 0.000 claims description 13
150000001413 amino acids Chemical class 0.000 claims description 12
125000003118 aryl group Chemical group 0.000 claims description 10
125000002431 aminoalkoxy group Chemical group 0.000 claims description 9
208000022362 bacterial infectious disease Diseases 0.000 claims description 9
239000008194 pharmaceutical composition Substances 0.000 claims description 9
229920006395 saturated elastomer Polymers 0.000 claims description 9
208000035143 Bacterial infection Diseases 0.000 claims description 8
125000003545 alkoxy group Chemical group 0.000 claims description 8
125000001188 haloalkyl group Chemical group 0.000 claims description 8
208000015181 infectious disease Diseases 0.000 claims description 8
230000000813 microbial effect Effects 0.000 claims description 8
125000001424 substituent group Chemical group 0.000 claims description 8
239000004471 Glycine Substances 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 7
125000005096 aminoalkylaminocarbonyl group Chemical group 0.000 claims description 7
125000005123 aminoalkylcarboxy group Chemical group 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
125000003277 amino group Chemical group 0.000 claims description 6
125000005416 guanidinoalkyloxy group Chemical group 0.000 claims description 5
125000003710 aryl alkyl group Chemical group 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical group C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims description 3
125000004423 acyloxy group Chemical group 0.000 claims description 3
235000004279 alanine Nutrition 0.000 claims description 3
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
150000003839 salts Chemical class 0.000 claims description 3
238000006467 substitution reaction Methods 0.000 claims description 3
AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 claims description 2
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235000018417 cysteine Nutrition 0.000 claims description 2
XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims description 2
239000003814 drug Substances 0.000 claims description 2
230000002708 enhancing effect Effects 0.000 claims description 2
238000000338 in vitro Methods 0.000 claims description 2
125000000979 2-amino-2-oxoethyl group Chemical group [H]C([*])([H])C(=O)N([H])[H] 0.000 claims 2
125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
125000002653 sulfanylmethyl group Chemical group [H]SC([H])([H])[*] 0.000 claims 1
125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 219
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235000019439 ethyl acetate Nutrition 0.000 description 69
239000002904 solvent Substances 0.000 description 69
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VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 43
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BHQCQFFYRZLCQQ-OELDTZBJSA-N cholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 BHQCQFFYRZLCQQ-OELDTZBJSA-N 0.000 description 31
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QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 18
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JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 17
QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 16
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YJQPYGGHQPGBLI-KGSXXDOSSA-N novobiocin Chemical compound O1C(C)(C)[C@H](OC)[C@@H](OC(N)=O)[C@@H](O)[C@@H]1OC1=CC=C(C(O)=C(NC(=O)C=2C=C(CC=C(C)C)C(O)=CC=2)C(=O)O2)C2=C1C YJQPYGGHQPGBLI-KGSXXDOSSA-N 0.000 description 16
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RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 15
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125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 14
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RIWRFSMVIUAEBX-UHFFFAOYSA-N n-methyl-1-phenylmethanamine Chemical compound CNCC1=CC=CC=C1 RIWRFSMVIUAEBX-UHFFFAOYSA-N 0.000 description 12
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