HISPIDIN

OC1=CC(=O)OC(\C=C\C2=CC=C(O)C(O)=C2)=C1

InChIKey=SGJNQVTUYXCBKH-HNQUOIGGSA-N

InChI=1S/C13H10O5/c14-9-6-10(18-13(17)7-9)3-1-8-2-4-11(15)12(16)5-8/h1-7,14-16H/b3-1+

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	1
Optical Activity	NONE

PubMed

Title	Date	PubMed
Isolation, structure, and HIV-1-integrase inhibitory activity of structurally diverse fungal metabolites.	2003 Dec	14714192
Regulation of skin microvasculature angiogenesis, cell migration, and permeability by a specific inhibitor of PKCalpha.	2006 Feb	16374459
A pharmacologically-based array to identify targets of cyclosporine A-induced toxicity in cultured renal proximal tubule cells.	2012 Jan 15	22155090
First-in-class small molecule inhibitors of the single-strand DNA cytosine deaminase APOBEC3G.	2012 Mar 16	22181350
p66Shc signaling is involved in stress responses elicited by anthracycline treatment of rat cardiomyoblasts.	2016 Jul	26318906

Substance Class	Chemical Created by `admin` on `Fri Dec 15 19:46:42 GMT 2023` Edited by `admin` on `Fri Dec 15 19:46:42 GMT 2023`
Record UNII	SSJ18CG55E
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

HISPIDIN

Common Name

English

2-((E)-2-(3,4-DIHYDROXYPHENYL)ETHENYL)-6-HYDROXYPYRAN-4-ONE

Systematic Name

English

Code System Code Type Description

WIKIPEDIA

HISPIDIN