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Chemical structure of CAS 83-72-7

2-Hydroxy-1,4-naphthoquinone

In Stock•Starting at $10 for 5 g•Purity ≥ 95%
CAS No.83-72-7
MDL No.MFCD00001678
MFC10H6O3
MW174.15
InChI KeyWVCHIGAIXREVNS-UHFFFAOYSA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
5 g95%$10In Stock
10 g98%$18In Stock
15 g98%$25In Stock
25 g98%$26In Stock
50 g98%$49In Stock
100 g98%$96In Stock
250 g98%$230In Stock
500 g98%$426In Stock
1 kg95%$785In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

Lawsone is a 1,4-naphthoquinone with a hydroxy group at the C-2 position. It is derived from the leaves of Lawsonia inermis and functions as a protective and antifungal agent. It is a tautomer of naphthalene-1,2,4-trione.

CAS No.83-72-7
Product Name2-Hydroxy-1,4-naphthoquinone
IrritantIrritant
Health HazardHealth Hazard
Signal Word:Warning
HCode:H302-H315-H319-H335-H341
PCode:P203-P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P318-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

Related Articles

Studies related to this compound and its mechanism of action

Biological evaluation of hydroxynaphthoquinones as anti-malarials.

Malaria journal • Vol. 12 • 2013
PMID: 23841934PMC: PMC3726445DOI: 10.1186/1475-2875-12-234

Discovery, total synthesis, HRV 3C-protease inhibitory activity, and structure-activity relationships of 2-methoxystypandrone and its analogues.

Bioorganic & medicinal chemistry letters • Vol. 11, Issue 24 • 2001
PMID: 11720861DOI: 10.1016/s0960-894x(01)00648-5

Antiretroviral agents as inhibitors of both human immunodeficiency virus type 1 integrase and protease.

Journal of medicinal chemistry • Vol. 39, Issue 13 • 1996
PMID: 8691444DOI: 10.1021/jm960074e

Hydroxyquinones are competitive non-peptide inhibitors of HIV-1 proteinase.

Biochimica et biophysica acta • Vol. 1253, Issue 1 • 1995
PMID: 7492599DOI: 10.1016/0167-4838(95)00183-u

Documentation

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