LAPACHONE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C15H14O3
Molecular Weight	242.2699
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of LAPACHONE

Structure Search

SMILES

CC1(C)CCC2=C(O1)C3=CC=CC=C3C(=O)C2=O

InChI

InChIKey=QZPQTZZNNJUOLS-UHFFFAOYSA-N

InChI=1S/C15H14O3/c1-15(2)8-7-11-13(17)12(16)9-5-3-4-6-10(9)14(11)18-15/h3-6H,7-8H2,1-2H3

HIDE SMILES / InChI

Molecular Formula	C15H14O3
Molecular Weight	242.2699
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:54:57 UTC 2023` Edited by `admin` on `Fri Dec 15 15:54:57 UTC 2023`
Record UNII	6N4FA2QQ6A
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

LAPACHONE

Official Name

English

LAPACHONE [INCI]

Common Name

English

BETA-LAP-WJ

Brand Name

English

ARQ-501

Code

English

NSC-26326

Code

English

3,4-DIHYDRO-2,2-DIMETHYL-2H-NAPHTHO(1,2-B)PYRAN-5,6-DIONE

Systematic Name

English

.BETA.-LAPACHONE

Common Name

English

NSC-629749

Code

English

Beta lapachone [WHO-DD]

Common Name

English

2H-NAPHTHO(1,2-B)PYRAN-5,6-DIONE, 3,4-DIHYDRO-2,2-DIMETHYL-

Systematic Name

English

MB-12066

Code

English

Classification Tree Code System Code

FDA ORPHAN DRUG

812821

Created by admin on Fri Dec 15 15:54:57 UTC 2023 , Edited by admin on Fri Dec 15 15:54:57 UTC 2023

NCI_THESAURUS

C274

Created by admin on Fri Dec 15 15:54:57 UTC 2023 , Edited by admin on Fri Dec 15 15:54:57 UTC 2023

Code System Code Type Description

PUBCHEM

3885

Created by admin on Fri Dec 15 15:54:57 UTC 2023 , Edited by admin on Fri Dec 15 15:54:57 UTC 2023

PRIMARY

EPA CompTox

DTXSID90197019

Created by admin on Fri Dec 15 15:54:57 UTC 2023 , Edited by admin on Fri Dec 15 15:54:57 UTC 2023

PRIMARY

FDA UNII

6N4FA2QQ6A

Created by admin on Fri Dec 15 15:54:57 UTC 2023 , Edited by admin on Fri Dec 15 15:54:57 UTC 2023

PRIMARY

CHEBI

10429

Created by admin on Fri Dec 15 15:54:57 UTC 2023 , Edited by admin on Fri Dec 15 15:54:57 UTC 2023

PRIMARY

CAS

4707-32-8

Created by admin on Fri Dec 15 15:54:57 UTC 2023 , Edited by admin on Fri Dec 15 15:54:57 UTC 2023

PRIMARY

DRUG BANK

DB11948

Created by admin on Fri Dec 15 15:54:57 UTC 2023 , Edited by admin on Fri Dec 15 15:54:57 UTC 2023

PRIMARY

NCI_THESAURUS

C28694

Created by admin on Fri Dec 15 15:54:57 UTC 2023 , Edited by admin on Fri Dec 15 15:54:57 UTC 2023

PRIMARY

NSC

629749

Created by admin on Fri Dec 15 15:54:57 UTC 2023 , Edited by admin on Fri Dec 15 15:54:57 UTC 2023

PRIMARY

NSC

26326

Created by admin on Fri Dec 15 15:54:57 UTC 2023 , Edited by admin on Fri Dec 15 15:54:57 UTC 2023

PRIMARY

Related Record Type Details


					6GLA1946WX

HANDROANTHUS IMPETIGINOSUS BARK

PARENT -> ACTIVE CONSTITUENT ALWAYS PRESENT

Amount:

Related Record Type Details


					W26Y36C65Y

2,2-DIMETHYL-3,4-DIHYDROPYRANO(3,2-C)ISOCHROMEN-6(2H)-ONE

METABOLITE -> PARENT

Comments:

IN VITRO


					JT2PE9HCP8

2-(5-FORMYL-2,2-DIMETHYL-3,4-DIHYDRO-2H-PYRAN-6-YL)BENZOIC ACID

METABOLITE -> PARENT

Comments:

IN VITRO

Amount:


					Q52LC8LNT3

6-(2-Carboxyphenyl)-3,4-dihydro-2,2-dimethyl-2H-pyran-5-carboxylic acid

METABOLITE -> PARENT

Comments:

IN VITRO

Amount:


					BVU5PQ5R6M

2,2-DIMETHYL-3,4-DIHYDRO-2H-INDENO(1,2-B)PYRAN-5 ONE

METABOLITE -> PARENT

Comments:

IN VITRO


					SXO757LF40

2,2-DIMETHYL-3,4-DIHYDRO-2H,5H-PYRANO(3,2-C)CHROMEN-5-ONE

METABOLITE -> PARENT

Comments:

IN VITRO

Amount:

Related Record Type Details


					6N4FA2QQ6A

LAPACHONE

ACTIVE MOIETY

Amount: