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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 E

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](O)[C@H]5OC(=O)CC6=CC=CC=C6

InChI

InChIKey=UDVVGDCMWCVRCO-WOPDTIQPSA-N
InChI=1S/C65H95NO21/c1-13-14-18-29-51-64(7,8)61(72)62(84-53(70)32-43-26-19-17-20-27-43)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 22:51:17 GMT 2025
Edited
by admin
on Mon Mar 31 22:51:17 GMT 2025
Record UNII
4PU25GRT71
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ANTIBIOTIC LL-E 19020.ALPHA.
Preferred Name English
PHENELFAMYCIN E
Common Name English
.ALPHA.-GANEFROMYCIN
Common Name English
GANEFROMYCIN COMPONENT (ALPHA)
Common Name English
GANEFROMYCIN .ALPHA.
Common Name English
Code System Code Type Description
FDA UNII
4PU25GRT71
Created by admin on Mon Mar 31 22:51:17 GMT 2025 , Edited by admin on Mon Mar 31 22:51:17 GMT 2025
PRIMARY
PUBCHEM
90478442
Created by admin on Mon Mar 31 22:51:17 GMT 2025 , Edited by admin on Mon Mar 31 22:51:17 GMT 2025
PRIMARY
CAS
114451-31-9
Created by admin on Mon Mar 31 22:51:17 GMT 2025 , Edited by admin on Mon Mar 31 22:51:17 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY