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Details

Stereochemistry UNKNOWN
Molecular Formula C51H64N12O12S2
Molecular Weight 1101.257
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ECHINOMYCIN

SMILES

CSC1SC[C@@H]2N(C)C(=O)[C@H](C)NC(=O)[C@@H](COC(=O)[C@H](C(C)C)N(C)C(=O)[C@H]1N(C)C(=O)[C@H](C)NC(=O)[C@@H](COC(=O)[C@H](C(C)C)N(C)C2=O)NC(=O)C3=NC4=C(C=CC=C4)N=C3)NC(=O)C5=NC6=C(C=CC=C6)N=C5

InChI

InChIKey=AUJXLBOHYWTPFV-VITLIGDRSA-N
InChI=1S/C51H64N12O12S2/c1-25(2)38-49(72)74-22-36(59-42(65)34-21-53-30-17-13-15-19-32(30)57-34)44(67)55-28(6)46(69)63(10)40-48(71)62(9)39(26(3)4)50(73)75-23-35(58-41(64)33-20-52-29-16-12-14-18-31(29)56-33)43(66)54-27(5)45(68)60(7)37(47(70)61(38)8)24-77-51(40)76-11/h12-21,25-28,35-40,51H,22-24H2,1-11H3,(H,54,66)(H,55,67)(H,58,64)(H,59,65)/t27-,28-,35+,36+,37-,38-,39-,40+,51?/m0/s1

HIDE SMILES / InChI

Molecular Formula C51H64N12O12S2
Molecular Weight 1101.257
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 8 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:25:34 UTC 2023
Edited
by admin
on Sat Dec 16 08:25:34 UTC 2023
Record UNII
TG824J6RQT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ECHINOMYCIN
MI  
Common Name English
NSC-13502
Code English
LEVOMYCIN
Common Name English
N-(2-QUINOXALINYLCARBONYL)-O-(N-(2-QUINOXALINYLCARBONYL)-D-SERYL-L-ALANYL-3-MERCAPTO-N,S-DIMETHYLCYSTEINYL-N-METHYL-L-VALYL)-D-SERYL-L-ALANYL-N-METHYLCYSTEINYL-N-METHYL L-VALINE (8->1)-LACTONE CYCLIC (3->7)-THIOESTER
Systematic Name English
QUINOMYCIN A
Common Name English
NSC-526417
Code English
SK-302B
Code English
ECHINOMYCIN [MI]
Common Name English
ANTIBIOTIC A-654I
Code English
L-VALINE, N-(2-QUINOXALINYLCARBONYL)-O-(N-(2-QUINOXALINYLCARBONYL)-D-SERYL-L-ALANYL-3-MERCAPTO-N,S-DIMETHYLCYSTEINYL-N-METHYL-L-VALYL)-D-SERYL-L-ALANYL-N-METHYLCYSTEINYL-N-METHYL-, (8->1)-LACTONE, CYCLIC (3->7)-THIOETHER
Systematic Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 479815
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
FDA ORPHAN DRUG 549016
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
NCI_THESAURUS C582
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
Code System Code Type Description
CAS
512-64-1
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY
FDA UNII
TG824J6RQT
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY
MESH
D004448
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY
NCI_THESAURUS
C462
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY
CAS
1403-88-9
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
ALTERNATIVE
WIKIPEDIA
ECHINOMYCIN
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY
SMS_ID
100000178234
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY
NSC
13502
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY
NSC
526417
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY
DRUG BANK
DB15582
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY
EPA CompTox
DTXSID5031266
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY
MERCK INDEX
m4814
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY Merck Index
PUBCHEM
6857732
Created by admin on Sat Dec 16 08:25:34 UTC 2023 , Edited by admin on Sat Dec 16 08:25:34 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY