U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C29H38N4O9.C16H18N2O5S
Molecular Weight 937.023
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PENIMEPICYCLINE

SMILES

[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@@]2([H])NC(=O)COC3=CC=CC=C3)C(O)=O.[H][C@@]45C[C@@]6([H])C(C(=O)C7=C(O)C=CC=C7[C@@]6(C)O)=C(O)[C@]4(O)C(=O)C(C(=O)NCN8CCN(CCO)CC8)=C(O)[C@H]5N(C)C

InChI

InChIKey=MEGKRPMNPGTIIG-VNYBMUHKSA-N
InChI=1S/C29H38N4O9.C16H18N2O5S/c1-28(41)15-5-4-6-18(35)19(15)23(36)20-16(28)13-17-22(31(2)3)24(37)21(26(39)29(17,42)25(20)38)27(40)30-14-33-9-7-32(8-10-33)11-12-34;1-16(2)12(15(21)22)18-13(20)11(14(18)24-16)17-10(19)8-23-9-6-4-3-5-7-9/h4-6,16-17,22,34-35,37-38,41-42H,7-14H2,1-3H3,(H,30,40);3-7,11-12,14H,8H2,1-2H3,(H,17,19)(H,21,22)/t16-,17-,22-,28+,29-;11-,12+,14-/m01/s1

HIDE SMILES / InChI
Penimepicycline is a salt of beta-lactam antibiotic penicillin V and tetracycline antibiotic pipacycline. Penimepicycline exerts a bactericidal action on the streptococci, and a bacteriostatic action on various gram-positive and gram-negative bacilli, as well as on the penicillin-resistant staphylococci. In the 1960s it was studied in Japan for the treatment of urological, respiratory, gynecological and other infections.

Approval Year

Patents
Name Type Language
PENIMEPICYCLINE
INN   MI   WHO-DD  
INN  
Official Name English
PENETRACYNE
Brand Name English
PENIMEPICYCLINE [MI]
Common Name English
CRISEOCIL
Brand Name English
Penimepicycline [WHO-DD]
Common Name English
GEOTRICYN
Brand Name English
MEPICYCLINE PENICILLINATE
Common Name English
penimepicycline [INN]
Common Name English
Classification Tree Code System Code
WHO-ATC J01AA10
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
WHO-VATC QJ01AA10
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
225-002-0
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY
MERCK INDEX
m868
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY Merck Index
SMS_ID
100000082501
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY
CHEBI
75258
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY
WIKIPEDIA
Penimepicycline
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY
CAS
4599-60-4
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY
FDA UNII
3RGQ4B6E87
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
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DRUG BANK
DB13264
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY
DRUG CENTRAL
2084
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY
NCI_THESAURUS
C166691
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY
EVMPD
SUB09668MIG
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID20905088
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY
MESH
C005470
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY
INN
1271
Created by admin on Sat Dec 16 17:52:58 GMT 2023 , Edited by admin on Sat Dec 16 17:52:58 GMT 2023
PRIMARY