AUSTALIDE B

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C26H34O8
Molecular Weight	474.5434
Optical Activity	( - )
Defined Stereocenters	6 / 6
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

COC1=C2C[C@H]3[C@](C)(C[C@@H](O)[C@]45O[C@@](CC[C@]34C)(OC)OC5(C)C)OC2=C(C)C6=C1C(=O)OC6

InChI

InChIKey=ZVFMDVFPBVFGPG-BLQNBILZSA-N

InChI=1S/C26H34O8/c1-13-15-12-31-21(28)18(15)20(29-6)14-10-16-23(4)8-9-25(30-7)33-22(2,3)26(23,34-25)17(27)11-24(16,5)32-19(13)14/h16-17,27H,8-12H2,1-7H3/t16-,17-,23-,24+,25+,26-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C26H34O8
Molecular Weight	474.5434
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	6 / 6
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
α-Glucosidase Inhibitors from the Fungus Aspergillus terreus 3.05358.	2015-11	26567949

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:57:15 GMT 2025` Edited by `admin` on `Mon Mar 31 19:57:15 GMT 2025`
Record UNII	W3CLL7NFD3
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

(-)-Austalide B

Preferred Name

English

AUSTALIDE B

Common Name

English

5H-3,5a-Epoxy-12H-furo[3,4-i]oxepino[4,3-a]xanthen-12-one, 1,2,3,6,7,7a,10,14,14a,14b-decahydro-6-hydroxy-3,13-dimethoxy-5,5,7a,9,14b-pentamethyl-, (3S,5aR,6R,7aS,14aR,14bR)-

Systematic Name

English

12H-3,5a-Epoxy-5H-furo[3,4-i]oxepino[4,3-a]xanthen-12-one, 1,2,3,6,7,7a,10,14,14a,14b-decahydro-6-hydroxy-3,13-dimethoxy-5,5,7a,9,14b-pentamethyl-, (3S,5aR,6R,7aS,14aR,14bR)-

Systematic Name

English

Code System Code Type Description

CAS

81543-02-4

Created by admin on Mon Mar 31 19:57:15 GMT 2025 , Edited by admin on Mon Mar 31 19:57:15 GMT 2025

PRIMARY

FDA UNII

W3CLL7NFD3

Created by admin on Mon Mar 31 19:57:15 GMT 2025 , Edited by admin on Mon Mar 31 19:57:15 GMT 2025

PRIMARY

PUBCHEM

157978

Created by admin on Mon Mar 31 19:57:15 GMT 2025 , Edited by admin on Mon Mar 31 19:57:15 GMT 2025

PRIMARY

EPA CompTox

DTXSID901002048

Created by admin on Mon Mar 31 19:57:15 GMT 2025 , Edited by admin on Mon Mar 31 19:57:15 GMT 2025

PRIMARY