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

Details

Stereochemistry ABSOLUTE
Molecular Formula C25H43N13O10
Molecular Weight 685.69
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of ENVIOMYCIN

SMILES

[H][C@@]1(CCNC(=N)N1)[C@]2([H])NC(=O)\C(NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@H](CNC2=O)NC(=O)C[C@@H](N)[C@H](O)CCN)=C\NC(N)=O

InChI

InChIKey=HPWIIERXAFODPP-GHBBWTPBSA-N
InChI=1S/C25H43N13O10/c26-3-1-16(41)10(27)5-17(42)33-12-6-31-23(47)18(11-2-4-30-24(28)37-11)38-20(44)13(7-32-25(29)48)34-21(45)14(8-39)36-22(46)15(9-40)35-19(12)43/h7,10-12,14-16,18,39-41H,1-6,8-9,26-27H2,(H,31,47)(H,33,42)(H,34,45)(H,35,43)(H,36,46)(H,38,44)(H3,28,30,37)(H3,29,32,48)/b13-7-/t10-,11-,12+,14+,15+,16-,18+/m1/s1

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including: https://www.ncbi.nlm.nih.gov/pubmed/2539957 | https://www.ncbi.nlm.nih.gov/pubmed/17571483

Enviomycin, antimicrobial drug, was isolated in Japan from fermentation broth of Syteptomyces griseoverticillatus var tuberacticus. This drug, a water-soluble, basic peptide, is effective against tubercle bacilli as well as some gram-positive and gram-negative bacteria. It is related to viomycin and cepreomycin in some of its physicochemical properties. It is used for the treatment of Mycobacterium avium caused lung diseases.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[A case of pulmonary Mycobacterium fortuitum infection successfully treated with Kampo treatments].
2006 Aug
[Case of pulmonary multi-drug resistant tuberculosis with left destroyed lung, treated with pneumonectomy].
2007 Jul
[Case of multi-drug resistant pulmonary tuberculosis with bilateral cavitary lesions successfully treated by surgical treatment].
2007 Nov
Patents

Sample Use Guides

1 g/day three times weekly
Route of Administration: Unknown
In Vitro Use Guide
Enviomycin is bactericidal against Mycobacterium avium strain 13887 with MIC=1.6 ug/ml.
Name Type Language
ENVIOMYCIN
INN   MART.   MI   WHO-DD  
INN  
Official Name English
((15-(3,6-DIAMINO-4-HYDROXYHEXANAMIDO)-3-(HEXAHYDRO-2-IMINO-4-PYRIMIDINYL)-9,12-BIS(HYDROXYMETHYL-2,5,8,11,14-PENTAOXO-1,4,7,10,13-PENTAAZACYCLOHEXADEC-6-YLIDENE)METHYL)UREA
Common Name English
ENVIOMYCIN [MI]
Common Name English
Enviomycin [WHO-DD]
Common Name English
enviomycin [INN]
Common Name English
TUBERACTINOMYCIN N
MI  
Common Name English
ENVIOMYCIN [MART.]
Common Name English
TUBERACTINOMYCIN N [MI]
Common Name English
Code System Code Type Description
DRUG CENTRAL
3180
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
SMS_ID
100000080241
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
ChEMBL
CHEMBL2146142
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
MERCK INDEX
m4924
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY Merck Index
FDA UNII
XU299C23A2
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
CAS
33103-22-9
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
EVMPD
SUB06554MIG
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
WIKIPEDIA
Enviomycin
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
EPA CompTox
DTXSID901027569
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
DRUG BANK
DB08993
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
INN
3577
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
NCI_THESAURUS
C169954
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
PUBCHEM
20055267
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
MESH
D004776
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY
MERCK INDEX
m11253
Created by admin on Fri Dec 15 16:19:48 GMT 2023 , Edited by admin on Fri Dec 15 16:19:48 GMT 2023
PRIMARY Merck Index