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Details

Stereochemistry UNKNOWN
Molecular Formula C36H53NO13
Molecular Weight 707.8049
Optical Activity UNSPECIFIED
Defined Stereocenters 13 / 14
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LUCIMYCIN

SMILES

[H][C@]12C[C@@H](O[C@]3([H])O[C@H](C)[C@@H](O)[C@H](N)[C@@H]3O)\C=C\C=C\C=C\C=C\CC(CCCC)OC(=O)\C=C\[C@H]4O[C@@H]4C[C@H](O)C[C@](O)(C[C@H](O)[C@H]1C(O)=O)O2

InChI

InChIKey=MUAOHYJGHYFDSA-YZMLMZOASA-N
InChI=1S/C36H53NO13/c1-3-4-12-23-13-10-8-6-5-7-9-11-14-24(48-35-33(42)31(37)32(41)21(2)46-35)18-28-30(34(43)44)25(39)20-36(45,50-28)19-22(38)17-27-26(49-27)15-16-29(40)47-23/h5-11,14-16,21-28,30-33,35,38-39,41-42,45H,3-4,12-13,17-20,37H2,1-2H3,(H,43,44)/b6-5+,9-7+,10-8+,14-11+,16-15+/t21-,22+,23?,24+,25+,26-,27-,28+,30-,31+,32-,33+,35+,36-/m1/s1

HIDE SMILES / InChI

Molecular Formula C36H53NO13
Molecular Weight 707.8049
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 13 / 14
E/Z Centers 0
Optical Activity UNSPECIFIED

Lucimycin (lucensomycin or etruscomycin) is a polyene antibiotic with antimycotic activity. Originally it was isolated from Streptomyces lucensis n. sp.

Approval Year

PubMed

PubMed

TitleDatePubMed
[On the antimycotic activity in vitro of a new antibiotic (etruscomycin) isolated from Streptomyces lucensis n. sp].
1962 Nov-Dec
In vitro studies with a new antimycotic agent: lucensomycin.
1962 Oct
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:02:51 GMT 2023
Edited
by admin
on Fri Dec 15 16:02:51 GMT 2023
Record UNII
3K1B4B63D0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LUCIMYCIN
INN  
INN  
Official Name English
ETRUSCOMYCIN
Common Name English
NSC-143257
Code English
lucimycin [INN]
Common Name English
FI-1163
Code English
LUCENSOMYCIN [MI]
Common Name English
ANTIBIOTIC FI-1163
Code English
LEUCENSOMYCIN
Common Name English
LUCENSOMYCIN
MI  
Common Name English
ETRUSCOMICINA
Common Name English
6,11,28-TRIOXATRICYCLO(22.3.1.05,7)OCTACOSA-8,14,16,18,20-PENTAENE-25-CARBOXYLIC ACID, 22-((3-AMINO-3,6-DIDEOXY-.BETA.-D-MANNOPYRANOSYL)OXY)-12-BUTYL-1,3,26-TRIHYDROXY-10-OXO-
Common Name English
Code System Code Type Description
FDA UNII
3K1B4B63D0
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
CAS
13058-67-8
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
PUBCHEM
118984381
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
CAS
1384655-66-6
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
ALTERNATIVE
ECHA (EC/EINECS)
235-950-7
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
NSC
143257
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
WIKIPEDIA
LUCIMYCIN
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
SMS_ID
300000034357
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
EPA CompTox
DTXSID201016933
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
INN
1360
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106433
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
MERCK INDEX
m6921
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY Merck Index
DRUG CENTRAL
3329
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
NCI_THESAURUS
C166679
Created by admin on Fri Dec 15 16:02:51 GMT 2023 , Edited by admin on Fri Dec 15 16:02:51 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY