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

Details

Stereochemistry ABSOLUTE
Molecular Formula C16H19N3O6
Molecular Weight 349.3386
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MITOMYCIN A

SMILES

COC1=C(C)C(=O)C2=C([C@@H](COC(N)=O)[C@@]3(OC)[C@H]4N[C@H]4CN23)C1=O

InChI

InChIKey=HYFMSAFINFJTFH-NGSRAFSJSA-N
InChI=1S/C16H19N3O6/c1-6-11(20)10-9(12(21)13(6)23-2)7(5-25-15(17)22)16(24-3)14-8(18-14)4-19(10)16/h7-8,14,18H,4-5H2,1-3H3,(H2,17,22)/t7-,8+,14+,16-/m1/s1

HIDE SMILES / InChI

Molecular Formula C16H19N3O6
Molecular Weight 349.3386
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Cardiotoxicity of mitomycin A, mitomycin C, and seven N7 analogs in vitro.
1992
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:03:55 GMT 2025
Edited
by admin
on Mon Mar 31 22:03:55 GMT 2025
Record UNII
87TMG6FJHV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MITOMYCIN A
MI  
Common Name English
NSC-75986
Preferred Name English
6-METHOXY ANALOG OF MITOMYCIN C
Common Name English
AZIRINO(2',3':3,4)PYRROLO(1,2-A)INDOLE-4,7-DIONE, 8-(((AMINOCARBONYL)OXY)METHYL)-1,1A,2,8,8A,8B-HEXAHYDRO-6,8A-DIMETHOXY-5-METHYL-, (1AS,8S,8AR,8BS)-
Systematic Name English
MITOMYCIN A [MI]
Common Name English
MITOMYCIN IMPURITY B [EP IMPURITY]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C663
Created by admin on Mon Mar 31 22:03:55 GMT 2025 , Edited by admin on Mon Mar 31 22:03:55 GMT 2025
Code System Code Type Description
MERCK INDEX
m7570
Created by admin on Mon Mar 31 22:03:55 GMT 2025 , Edited by admin on Mon Mar 31 22:03:55 GMT 2025
PRIMARY Merck Index
NCI_THESAURUS
C1164
Created by admin on Mon Mar 31 22:03:55 GMT 2025 , Edited by admin on Mon Mar 31 22:03:55 GMT 2025
PRIMARY NCIT
CAS
4055-39-4
Created by admin on Mon Mar 31 22:03:55 GMT 2025 , Edited by admin on Mon Mar 31 22:03:55 GMT 2025
PRIMARY
FDA UNII
87TMG6FJHV
Created by admin on Mon Mar 31 22:03:55 GMT 2025 , Edited by admin on Mon Mar 31 22:03:55 GMT 2025
PRIMARY
HSDB
3418
Created by admin on Mon Mar 31 22:03:55 GMT 2025 , Edited by admin on Mon Mar 31 22:03:55 GMT 2025
PRIMARY
PUBCHEM
19972
Created by admin on Mon Mar 31 22:03:55 GMT 2025 , Edited by admin on Mon Mar 31 22:03:55 GMT 2025
PRIMARY
EPA CompTox
DTXSID201318131
Created by admin on Mon Mar 31 22:03:55 GMT 2025 , Edited by admin on Mon Mar 31 22:03:55 GMT 2025
PRIMARY
NSC
75986
Created by admin on Mon Mar 31 22:03:55 GMT 2025 , Edited by admin on Mon Mar 31 22:03:55 GMT 2025
PRIMARY
CHEBI
84589
Created by admin on Mon Mar 31 22:03:55 GMT 2025 , Edited by admin on Mon Mar 31 22:03:55 GMT 2025
PRIMARY
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