PEROXISOMICINE A1

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C30H26O8
Molecular Weight	514.5226
Optical Activity	UNSPECIFIED
Additional Stereochemistry	Yes
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0
Stereo Comments	AXIAL, S

SHOW SMILES / InChI

Structure Search

SMILES

C[C@@]1(O)CC(=O)C2=C(O)C3=C(C=CC(=C3O)C4=C5C=CC=C(O)C5=C(O)C6=C4C[C@](C)(O)CC6=O)C=C2C1

InChI

InChIKey=FBPZAGOTWAVQJH-KYJUHHDHSA-N

InChI=1S/C30H26O8/c1-29(37)9-14-8-13-6-7-16(26(34)22(13)27(35)21(14)19(32)11-29)23-15-4-3-5-18(31)24(15)28(36)25-17(23)10-30(2,38)12-20(25)33/h3-8,31,34-38H,9-12H2,1-2H3/t29-,30-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C30H26O8
Molecular Weight	514.5226
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
Antimicrobial activity of coupled hydroxyanthracenones isolated from plants of the genus Karwinskia.	2006-07	16797144

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:04:48 GMT 2025` Edited by `admin` on `Mon Mar 31 21:04:48 GMT 2025`
Record UNII	Q308RHT4PV
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

PEROXISOMICINE A1

Common Name

English

T-514

Preferred Name

English

(2,9'-BIANTHRACENE)-4',8(1'H,5H)-DIONE, 2',3',6,7-TETRAHYDRO-2',6-DIMETHYL-1,2',5',6,9,10'-HEXAHYDROXY-

Systematic Name

English

(2,9'-BIANTHRACENE)-4',8(1'H,5H)-DIONE, 2',3',6,7-TETRAHYDRO-1,2',5',6,9,10'-HEXAHYDROXY-2',6-DIMETHYL-, (2S,2'S,6S)-

Systematic Name

English

TOXIN T-514

Code

English

Code System Code Type Description

FDA UNII

Q308RHT4PV

Created by admin on Mon Mar 31 21:04:48 GMT 2025 , Edited by admin on Mon Mar 31 21:04:48 GMT 2025

PRIMARY

CAS

110270-61-6

Created by admin on Mon Mar 31 21:04:48 GMT 2025 , Edited by admin on Mon Mar 31 21:04:48 GMT 2025

PRIMARY

PUBCHEM

11386735

Created by admin on Mon Mar 31 21:04:48 GMT 2025 , Edited by admin on Mon Mar 31 21:04:48 GMT 2025

PRIMARY

EPA CompTox

DTXSID40911565

Created by admin on Mon Mar 31 21:04:48 GMT 2025 , Edited by admin on Mon Mar 31 21:04:48 GMT 2025

PRIMARY