LANKACIDINOL

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 Search

SMILES

C[C@H](O)C(=O)N[C@@H]1\C=C(C)\C=C\[C@@H](O)C\C=C(C)\C=C\[C@@H](O)C[C@H]2OC(=O)[C@]1(C)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 `Mon Mar 31 22:24:02 GMT 2025` Edited by `admin` on `Mon Mar 31 22:24:02 GMT 2025`
Record UNII	35456Z39CA
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LANKACIDINOL

Common Name

English

ANTIBIOTIC T 2636F

Preferred Name

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 Mon Mar 31 22:24:02 GMT 2025 , Edited by admin on Mon Mar 31 22:24:02 GMT 2025

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FDA UNII

35456Z39CA

Created by admin on Mon Mar 31 22:24:02 GMT 2025 , Edited by admin on Mon Mar 31 22:24:02 GMT 2025

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EPA CompTox

DTXSID501099334

Created by admin on Mon Mar 31 22:24:02 GMT 2025 , Edited by admin on Mon Mar 31 22:24:02 GMT 2025

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PUBCHEM

121225227

Created by admin on Mon Mar 31 22:24:02 GMT 2025 , Edited by admin on Mon Mar 31 22:24:02 GMT 2025

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