NAPHTHORESORCINOL

OC1=CC(O)=C2C=CC=CC2=C1

InChIKey=XOOMNEFVDUTJPP-UHFFFAOYSA-N

InChI=1S/C10H8O2/c11-8-5-7-3-1-2-4-9(7)10(12)6-8/h1-6,11-12H

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

PubMed

Title	Date	PubMed
Selective nonpeptidic inhibitors of herpes simplex virus type 1 and human cytomegalovirus proteases.	2001 Mar	11256477
Enantioselective DNA alkylation by a pyrrole-imidazole S-CBI conjugate.	2004 Jul 28	15264825
Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products.	2005 Jun 16	15959519
Effector-repressor interactions, binding of a single effector molecule to the operator-bound TtgR homodimer mediates derepression.	2006 Mar 17	16407274
rac-(1S,2R)-Diethyl 6-hydr-oxy-1-(4-methoxy-phen-yl)-3-oxo-2,3-di-hydro-1H-benzo[f]chromen-2-yl]-phospho-nate.	2008 Jun 7	21202876
Antibiotic pigment from desert soil actinomycetes; biological activity, purification and chemical screening.	2009 Sep	20502566
Functional characterization of the promiscuous prenyltransferase responsible for furaquinocin biosynthesis: identification of a physiological polyketide substrate and its prenylated reaction products.	2010 Dec 17	20937800

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:34:45 GMT 2023` Edited by `admin` on `Fri Dec 15 18:34:45 GMT 2023`
Record UNII	5X457YEW8Y
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

NAPHTHORESORCINOL

Common Name

English

NSC-115890

Code

English

1,3-NAPHTHALENEDIOL

Systematic Name

English

1,3-DIHYDROXYNAPHTHALENE

Systematic Name

English

NAPHTHORESORCINOL [MI]

Common Name

English

Code System Code Type Description

ECHA (EC/EINECS)

205-079-7