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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H35NO7
Molecular Weight 461.5479
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LANKACIDINOL

SMILES

[H][C@]12C[C@H](O)\C=C\C(C)=C\C[C@H](O)\C=C\C(C)=C\[C@@H](NC(=O)[C@H](C)O)[C@](C)(C(=O)O1)C(=O)[C@@H]2C

InChI

InChIKey=FUDDPCATVZFGCZ-UBCGEOKZSA-N
InChI=1S/C25H35NO7/c1-14-6-9-18(28)10-8-15(2)12-21(26-23(31)17(4)27)25(5)22(30)16(3)20(33-24(25)32)13-19(29)11-7-14/h6-8,10-12,16-21,27-29H,9,13H2,1-5H3,(H,26,31)/b10-8+,11-7+,14-6+,15-12+/t16-,17+,18+,19-,20-,21-,25+/m1/s1

HIDE SMILES / InChI

Molecular Formula C25H35NO7
Molecular Weight 461.5479
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:57:27 GMT 2023
Edited
by admin
on Sat Dec 16 08:57:27 GMT 2023
Record UNII
35456Z39CA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LANKACIDINOL
Common Name English
ANTIBIOTIC T 2636F
Code English
LACTAMIDE, N-(7,13-DIHYDROXY-1,4,10,19-TETRAMETHYL-17,18-DIOXO-16-OXABICYCLO(13.2.2)NONADECA-3,5,9,11-TETRAEN-2-YL)-, (ALL-E)-(1S,2R,7S,13S,15R,19R)-(-)-
Systematic Name English
LANKACIDINOL, (-)-
Common Name English
PROPANAMIDE, N-((1S,2R,3E,5E,7S,9E,11E,13S,15R,19R)-7,13-DIHYDROXY-1,4,10,19-TETRAMETHYL-17,18-DIOXO-16-OXABICYCLO(13.2.2)NONADECA-3,5,9,11-TETRAEN-2-YL)-2-HYDROXY-, (2S)-
Systematic Name English
Code System Code Type Description
CAS
23498-37-5
Created by admin on Sat Dec 16 08:57:27 GMT 2023 , Edited by admin on Sat Dec 16 08:57:27 GMT 2023
PRIMARY
FDA UNII
35456Z39CA
Created by admin on Sat Dec 16 08:57:27 GMT 2023 , Edited by admin on Sat Dec 16 08:57:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID50109933
Created by admin on Sat Dec 16 08:57:27 GMT 2023 , Edited by admin on Sat Dec 16 08:57:27 GMT 2023
PRIMARY
PUBCHEM
121225227
Created by admin on Sat Dec 16 08:57:27 GMT 2023 , Edited by admin on Sat Dec 16 08:57:27 GMT 2023
PRIMARY