ERYTHRO-9-(2-HYDROXY-3-NONYL)ADENINE MONOHYDROCHLORIDE, (+)-

Cl.CCCCCC[C@H]([C@H](C)O)N1C=NC2=C1N=CN=C2N

InChIKey=VVDXNJRUNJMYOZ-VZXYPILPSA-N

InChI=1S/C14H23N5O.ClH/c1-3-4-5-6-7-11(10(2)20)19-9-18-12-13(15)16-8-17-14(12)19;/h8-11,20H,3-7H2,1-2H3,(H2,15,16,17);1H/t10-,11+;/m0./s1

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

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

Targets

Primary Target	Pharmacology	Condition	Potency
Adenosine deaminase 13 Target ID: CHEMBL1910 Sources: https://www.ncbi.nlm.nih.gov/pubmed/7082355	Inhibitor 8297		2.0 nM [Ki]
Phosphodiesterase 2A 7 Target ID: CHEMBL2652 Sources: https://www.ncbi.nlm.nih.gov/pubmed/8519602 \| https://www.ncbi.nlm.nih.gov/pubmed/8730511	Inhibitor 8297		0.8 µM [IC50]

Substance Class	Chemical Created by `admin` on `Sat Dec 16 11:13:16 GMT 2023` Edited by `admin` on `Sat Dec 16 11:13:16 GMT 2023`
Record UNII	5LD6S82A2N
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

ERYTHRO-9-(2-HYDROXY-3-NONYL)ADENINE MONOHYDROCHLORIDE, (+)-

Common Name

English

EHNA HYDROCHLORIDE, (+)-

Common Name

English

9H-PURINE-9-ETHANOL, 6-AMINO-.BETA.-HEXYL-.ALPHA.-METHYL-, MONOHYDROCHLORIDE, (S-(R*,S*))

Systematic Name

English

Code System Code Type Description

CAS

81408-45-9

Created by admin on Sat Dec 16 11:13:16 GMT 2023 , Edited by admin on Sat Dec 16 11:13:16 GMT 2023

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PUBCHEM

24197375

Created by admin on Sat Dec 16 11:13:16 GMT 2023 , Edited by admin on Sat Dec 16 11:13:16 GMT 2023

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FDA UNII

5LD6S82A2N

Created by admin on Sat Dec 16 11:13:16 GMT 2023 , Edited by admin on Sat Dec 16 11:13:16 GMT 2023

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