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Details

Stereochemistry RACEMIC
Molecular Formula C59H103N3O18
Molecular Weight 1142.4584
Optical Activity ( + / - )
Defined Stereocenters 0 / 22
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of Scopafungin

SMILES

CC(CCC\C=C\CCCN(C)C(N)=N)CC(C)C1OC(=O)C(C)C(O)\C=C\C(C)C(O)C(C)C(O)C(C)C(O)CCCC(O)CC2(O)OC(CC(O)C2O)CC(CC(O)CC(O)C(C)C(O)\C=C\C=C\C1C)OC(=O)CC(O)=O

InChI

InChIKey=RSODTZFJSFMTPQ-NBURPXERSA-N
InChI=1S/C59H103N3O18/c1-34(19-14-12-10-11-13-17-26-62(9)58(60)61)27-37(4)55-36(3)20-15-16-22-46(65)38(5)49(68)29-43(64)28-44(78-52(72)32-51(70)71)30-45-31-50(69)56(75)59(77,80-45)33-42(63)21-18-23-47(66)39(6)54(74)41(8)53(73)35(2)24-25-48(67)40(7)57(76)79-55/h10-11,15-16,20,22,24-25,34-50,53-56,63-69,73-75,77H,12-14,17-19,21,23,26-33H2,1-9H3,(H3,60,61)(H,70,71)/b11-10+,20-15+,22-16+,25-24+

HIDE SMILES / InChI

Molecular Formula C59H103N3O18
Molecular Weight 1142.4584
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 22
E/Z Centers 1
Optical Activity UNSPECIFIED

Scopafungin (also known as GE4800) is an inhibitor of oxidative phosphorylation in mitochondria. Scopafungin also inhibits, in vitro, a variety of pathogenic fungi, yeasts, and gram-positive bacteria.

Approval Year

PubMed

PubMed

TitleDatePubMed
Scopafungin, a crystalline antibiotic produced by Streptomyces hygroscopicus var. enhygrus var. nova.
1971 Sep
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:53:55 GMT 2023
Edited
by admin
on Sat Dec 16 09:53:55 GMT 2023
Record UNII
LOE3K7R62G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Scopafungin
USAN  
USAN  
Official Name English
ANTIBIOTIC DERIVED FROM STREPTOMYCES HYGROSCOPICUS VARIANT
Common Name English
NIPHIMYCIN I.ALPHA.
Common Name English
SCOPAFUNGIN [USAN]
Common Name English
U-29479
Code English
NSC-107041
Code English
PROPANEDIOIC ACID, 1-(5,7,9,19,23,25,27,31,33,34,35-UNDECAHYDROXY-15-(11-((IMINO(METHYLAMINO)METHYL)AMINO)-1,3-DIMETHYL-7-UNDECEN-1-YL)-8,14,18,22,26,30-HEXAMETHYL-17-OXO-16,37-DIOXABICYCLO(31.3.1)HEPTATRIACONTA-10,12,20-TRIEN-3-YL) ESTER
Common Name English
U-29,479
Code English
Classification Tree Code System Code
NCI_THESAURUS C514
Created by admin on Sat Dec 16 09:53:55 GMT 2023 , Edited by admin on Sat Dec 16 09:53:55 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2103935
Created by admin on Sat Dec 16 09:53:55 GMT 2023 , Edited by admin on Sat Dec 16 09:53:55 GMT 2023
PRIMARY
NCI_THESAURUS
C152311
Created by admin on Sat Dec 16 09:53:55 GMT 2023 , Edited by admin on Sat Dec 16 09:53:55 GMT 2023
PRIMARY
PUBCHEM
9963519
Created by admin on Sat Dec 16 09:53:55 GMT 2023 , Edited by admin on Sat Dec 16 09:53:55 GMT 2023
PRIMARY
CAS
1059503-09-1
Created by admin on Sat Dec 16 09:53:55 GMT 2023 , Edited by admin on Sat Dec 16 09:53:55 GMT 2023
ALTERNATIVE
CAS
11056-18-1
Created by admin on Sat Dec 16 09:53:55 GMT 2023 , Edited by admin on Sat Dec 16 09:53:55 GMT 2023
PRIMARY
FDA UNII
LOE3K7R62G
Created by admin on Sat Dec 16 09:53:55 GMT 2023 , Edited by admin on Sat Dec 16 09:53:55 GMT 2023
PRIMARY
EPA CompTox
DTXSID301318310
Created by admin on Sat Dec 16 09:53:55 GMT 2023 , Edited by admin on Sat Dec 16 09:53:55 GMT 2023
PRIMARY
NSC
107041
Created by admin on Sat Dec 16 09:53:55 GMT 2023 , Edited by admin on Sat Dec 16 09:53:55 GMT 2023
PRIMARY
KEGG
D05809
Created by admin on Sat Dec 16 09:53:55 GMT 2023 , Edited by admin on Sat Dec 16 09:53:55 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY