lapachol (Q739601)

inferred from SMILES

chemical formula

C₁₅H₁₄O₃

2 references

CC(=CCC1=C(C2=CC=CC=C2C(=O)C1=O)O)C

2 references

Russian Wikipedia

PubChem

CC(=CCC1=C(C(=O)c2ccccc2C1=O)O)C

0 references

found in taxon

Tectona grandis

4 references

Occupational allergic contact dermatitis caused by decorative plants

A 1,4-Anthraquinone derivative from Tectona grandis

5-Hydroxylapachol: a cytotoxic agent from Tectona grandis

Chemical components of the roots of Tectona grandis and Gmelina arborea

Tabebuia rosea

6 references

Naphthoquinone Constituents of Commercial Lapacho/Pau d'arco/Taheebo Products

Naphthoquinone Constituents of Tabebuia spp

Constituents of tabebuia guayacan—II

A new naphthaquinone from Tabebuia guayacan

Chemical examination of the roots of Tabebuia rosea and heartwood of Oroxylum indicum

Quinones and other constituents from Tabebuia rosea

Handroanthus impetiginosum

6 references

HPLC separation and determination of naphtho[2,3-b]furan-4,9-diones and related compounds in extracts of Tabebuia avellanedae (Bignoniaceae)

High-performance liquid chromatographic separation of some naturally occurring naphtoquinones and anthraquinones

Structure Determination of New Isomeric Naphtho[2,3-b]furan-4,9-diones fromTabebuia avellanedae by the selective-INEPT technique

Production of anti-tumour-promoting furanonaphthoquinones in Tabebuia avellanedae cell cultures

Synthesis and evaluation of bioactive naphthoquinones from the Brazilian medicinal plant, Tabebuia avellanedae

Selective growth-inhibiting effects of compounds identified in Tabebuia impetiginosa inner bark on human intestinal bacteria

Handroanthus impetiginosus

6 references

HPLC separation and determination of naphtho[2,3-b]furan-4,9-diones and related compounds in extracts of Tabebuia avellanedae (Bignoniaceae)

High-performance liquid chromatographic separation of some naturally occurring naphtoquinones and anthraquinones

Structure Determination of New Isomeric Naphtho[2,3-b]furan-4,9-diones fromTabebuia avellanedae by the selective-INEPT technique

Production of anti-tumour-promoting furanonaphthoquinones in Tabebuia avellanedae cell cultures

Synthesis and evaluation of bioactive naphthoquinones from the Brazilian medicinal plant, Tabebuia avellanedae

Selective growth-inhibiting effects of compounds identified in Tabebuia impetiginosa inner bark on human intestinal bacteria

Tabebuia impetiginosa

5 references

HPLC separation and determination of naphtho[2,3-b]furan-4,9-diones and related compounds in extracts of Tabebuia avellanedae (Bignoniaceae)

High-performance liquid chromatographic separation of some naturally occurring naphtoquinones and anthraquinones

Structure Determination of New Isomeric Naphtho[2,3-b]furan-4,9-diones fromTabebuia avellanedae by the selective-INEPT technique

Production of anti-tumour-promoting furanonaphthoquinones in Tabebuia avellanedae cell cultures

Selective growth-inhibiting effects of compounds identified in Tabebuia impetiginosa inner bark on human intestinal bacteria

Diphysa americana

1 reference

Isolation of lapachol from Diphysa robinoides

Diphysa robinioides

1 reference

Isolation of lapachol from Diphysa robinoides

Tabebuia ochracea

1 reference

Furanonaphthoquinones from Tabebuia ochracea

Newbouldia laevis

4 references

Naphthaquinones and an alkaloid from roots of Newbouldia laevis

Antifungal and antibacterial naphthoquinones from Newbouldia laevis roots.

Newbouldiaquinone and newbouldiamide: a new naphthoquinone-anthraquinone coupled pigment and a new ceramide from Newbouldia laevis

Newbouldiaquinone A: A naphthoquinone-anthraquinone ether coupled pigment, as a potential antimicrobial and antimalarial agent from Newbouldia laevis

Oroxylum indicum

1 reference

Antimicrobial and antiinflammatory activities of extracts and constituents of Oroxylum indicum (L.) Vent

Handroanthus chrysotrichus

1 reference

Phytochemical and analgesic investigation of Tabebuia chrysotricha

Tabebuia chrysotricha

1 reference

Phytochemical and analgesic investigation of Tabebuia chrysotricha

Bauhinia guianensis

1 reference

Constituents of the stem bark of Bauhinia guianensis

Schnella guianensis

1 reference

Constituents of the stem bark of Bauhinia guianensis

Dolichandra unguis-cati

2 references

Chemical characterization and biological activity of Macfadyena unguis-cati (Bignoniaceae)

Quinones and Other Constituents of Markhamia platycalyx and Bignonia unguiscati

Macfadyena unguis-cati

2 references

Chemical characterization and biological activity of Macfadyena unguis-cati (Bignoniaceae)

Quinones and Other Constituents of Markhamia platycalyx and Bignonia unguiscati

Tecomella undulata

3 references

A New Ferulic Ester fromTecomella undulata

6-O-veratryl catalposide: A new iridoid glucoside from Tecomella undulata

QUINONES AND OTHER CONSTITUENTS FROM THE ROOTS OFTECOMELLA UNDULATA

Markhamia lutea

1 reference

Quinones and Other Constituents of Markhamia platycalyx and Bignonia unguiscati

Markhamia platycalyx

1 reference

Quinones and Other Constituents of Markhamia platycalyx and Bignonia unguiscati

Stereospermum kunthianum

1 reference

Chemical constituents of the stem heart wood of Stereospermum kunthianum

Catalpa longissima

1 reference

Phytochemical Investigation of Cassia laevigata Pods, Part I

1 reference

1 reference

Spasmolytic activity of lapachol and its derivatives, α and β-lapachone, on the guinea-pig ileum involves blockade of voltage-gated calcium channels

Markhamia tomentosa

1 reference

Antiprotozoal activities of some constituents of Markhamia tomentosa (Bignoniaceae).

Markhamia stipulata

2 references

Phenolic glycosides from Markhamia stipulata

Chemical Constituents of the Stem Heartwood of Markhamia stipulata

Handroanthus guayacan

2 references

Constituents of tabebuia guayacan—II

A new naphthaquinone from Tabebuia guayacan

Tabebuia guayacan

2 references

Constituents of tabebuia guayacan—II

A new naphthaquinone from Tabebuia guayacan

Plenckia populnea

1 reference

Constituents of the root wood of Austroplenckia populnea var. ovata

Talipariti tiliaceum

1 reference

Naturally occurring quinones. Part 28. Sesquiterpenoid quinones and related compounds from Hibiscus tiliaceus

Hibiscus tiliaceus

1 reference

Naturally occurring quinones. Part 28. Sesquiterpenoid quinones and related compounds from Hibiscus tiliaceus

Plumbago zeylanica

1 reference

Difuranonaphthoquinones from Plumbago zeylanica roots

Avicennia germinans

1 reference

Gewinnung von Lapachol aus dem Kernholz von Avicennia tomentosa

Radermachera sinica

1 reference

Cybistax antisyphilitica

1 reference

Larvicidal activity of Cybistax antisyphilitica against Aedes aegypti larvae.

Stereospermum colais

1 reference

Free-radical-scavenging and xanthine oxidase inhibitory constituents from Stereospermum personatum

Stereospermum tetragonum

1 reference

Free-radical-scavenging and xanthine oxidase inhibitory constituents from Stereospermum personatum

Phyllarthron comorense

1 reference

Quinones and other constituents from Phyllarthron comorense

Diphysa carthagenensis

1 reference

Isolation of lapachol from Diphysa robinoides

Kigelia africana

3 references

Antibacterial and antifungal compounds from Kigelia pinnata

A naphthoquinone and a lignan from the wood of Kigelia pinnata

Isolation and structure of two new dihydroisocoumarins from Kigelia pinnata

Avicennia officinalis

1 reference

Gewinnung von Lapachol aus dem Kernholz von Avicennia tomentosa

Avicennia schaueriana

1 reference

Gewinnung von Lapachol aus dem Kernholz von Avicennia tomentosa

subject has role

anthelmintic

1 reference

15 March 2018

1 reference

15 March 2018

1 reference

15 March 2018

1 reference

15 March 2018

1 reference

phytogenic antineoplastic agents

MeSH descriptor ID

C008252

retrieved

15 March 2018

1 reference

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

15 March 2018

2914.69.10

0 references

0 references

0 references

Lapachol

0 references

Identifiers

InChI

1 reference

PubChem

1 reference

PubChem

1 reference

ChEBI release 2020-09-01

CAS Registry Number

84-79-7

2 references

Russian Wikipedia

https://commonchemistry.cas.org/detail?cas_rn=84-79-7

9 April 2021

ChemSpider ID

10770962

1 reference

Spanish Wikipedia

PubChem CID

3884

2 references

English Wikipedia

ChEBI ID

6377

mapping relation type

exact match

2 references

ChEBI release 2019-10-02

ChEBI release 2021-03-01

ChEMBL ID

CHEMBL15193

1 reference

2 references

SCHEMBL157256

2 references

splash10-000i-0950000000-2e024a87bfc4be7459db

1 reference

MassBank accession ID

MSBNK-Fiocruz-FIO00558

0 references

MSBNK-Fiocruz-FIO00559

0 references

MSBNK-Fiocruz-FIO00560

0 references

MSBNK-Fiocruz-FIO00561

0 references

MSBNK-Fiocruz-FIO00562

0 references

MSBNK-Fiocruz-FIO00563

0 references

MSBNK-Fiocruz-FIO00564

0 references

MSBNK-Fiocruz-FIO00565

0 references

MSBNK-Fiocruz-FIO00566

0 references

MSBNK-Fiocruz-FIO00567

0 references

SPLASH

0 references

splash10-052r-0900000000-d5fea52254a2b1e8bcf6

0 references

splash10-0a4i-0900000000-5d8ac013ea28f83f11b4

0 references

splash10-0a4i-0900000000-a53bf09a8180571f2513

0 references

splash10-0a4i-0910000000-5ac03881e6f9e00a8a42

0 references

splash10-052r-0910000000-adb4cd835c8779d60287

0 references

splash10-000i-0970000000-1b64510b4e1f8d87459b

0 references

NMRShiftDB structure ID

30100947

1 reference

DSSTox substance ID

DTXSID6049430

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

201-563-7

1 reference

ECHA Substance Infocard ID

Spanish Wikipedia

100.001.421

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.001.421

retrieved

27 December 2018

title

2-hydroxy-3-(3-methylbut-2-enyl)-1,4-naphthoquinone (English)

quotation

CAS no.: 84-79-7 (English)

MeSH descriptor ID

C008252

1 reference

Human Metabolome Database ID

MeSH descriptor ID

C008252

retrieved

14 March 2018

HMDB0253978

2 references

KNApSAcK ID

C00002835

2 references

UNII

B221938VB6

1 reference