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Details

Stereochemistry ABSOLUTE
Molecular Formula C65H95NO21
Molecular Weight 1226.4439
Optical Activity UNSPECIFIED
Defined Stereocenters 22 / 22
E/Z Centers 7
Charge 0

SHOW SMILES / InChI
Structure of PHENELFAMYCIN F

SMILES

CO[C@@H]([C@@H](C)[C@H]1C[C@H](O)[C@@H](O1)\C=C\C=C\C=C\C(O)=O)C(\C)=C\C=C\CNC(=O)[C@@H](CO[C@H]2C[C@H](OC)[C@H](O[C@@H]3C[C@@H](OC)[C@@H](O[C@H]4C[C@H](OC)[C@H](O)[C@H](C)O4)[C@H](C)O3)[C@H](C)O2)[C@@]5(O)O[C@@H](\C=C\C=C/C)C(C)(C)[C@@H](OC(=O)CC6=CC=CC=C6)[C@H]5O

InChI

InChIKey=LNHMLFJFDISYQH-YXDAFIJTSA-N
InChI=1S/C65H95NO21/c1-13-14-18-29-51-64(7,8)62(84-53(70)32-43-26-19-17-20-27-43)61(72)65(74,87-51)44(63(73)66-31-24-23-25-38(2)58(78-12)39(3)47-33-45(67)46(83-47)28-21-15-16-22-30-52(68)69)37-79-54-35-49(76-10)59(41(5)81-54)86-56-36-50(77-11)60(42(6)82-56)85-55-34-48(75-9)57(71)40(4)80-55/h13-30,39-42,44-51,54-62,67,71-72,74H,31-37H2,1-12H3,(H,66,73)(H,68,69)/b14-13-,16-15+,24-23+,28-21+,29-18+,30-22+,38-25+/t39-,40-,41-,42-,44+,45-,46-,47+,48-,49-,50+,51-,54+,55-,56+,57+,58+,59+,60-,61+,62-,65+/m0/s1

HIDE SMILES / InChI

Molecular Formula C65H95NO21
Molecular Weight 1226.4439
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 22 / 22
E/Z Centers 7
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:46:31 GMT 2025
Edited
by admin
on Mon Mar 31 22:46:31 GMT 2025
Record UNII
1X22T0CMC5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENELFAMYCIN F
Common Name English
ANTIBIOTIC LL-E 19020.BETA.
Preferred Name English
GANEFROMYCIN COMPONENT (BETA)
Common Name English
.BETA.-GANEFROMYCIN
Common Name English
GANEFROMYCIN .BETA.
Common Name English
Code System Code Type Description
FDA UNII
1X22T0CMC5
Created by admin on Mon Mar 31 22:46:31 GMT 2025 , Edited by admin on Mon Mar 31 22:46:31 GMT 2025
PRIMARY
CAS
114451-30-8
Created by admin on Mon Mar 31 22:46:31 GMT 2025 , Edited by admin on Mon Mar 31 22:46:31 GMT 2025
PRIMARY
PUBCHEM
90478571
Created by admin on Mon Mar 31 22:46:31 GMT 2025 , Edited by admin on Mon Mar 31 22:46:31 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY