MDOH hydrochloride

Details

Stereochemistry	RACEMIC
Molecular Formula	C10H13NO3.ClH
Molecular Weight	231.676
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

Cl.CC(CC1=CC2=C(OCO2)C=C1)NO

InChI

InChIKey=DMBCJQVFXIKFJX-UHFFFAOYSA-N

InChI=1S/C10H13NO3.ClH/c1-7(11-12)4-8-2-3-9-10(5-8)14-6-13-9;/h2-3,5,7,11-12H,4,6H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula	C10H13NO3
Molecular Weight	195.2151
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Molecular Formula	ClH
Molecular Weight	36.461
Charge	0
Count

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

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Serotonin 2a (5-HT2a) receptor 231 Target ID: CHEMBL224 Sources: Johnson Bankole A., Addiction Medicine: Science and Practice, V.1 retrieved from: https://books.google.ru/books?id=zvbr4Zn9S9MC&pg=PA594&lpg=PA594&dq=N-HYDROXY-3,4-METHYLENEDIOXYAMPHETAMINE+receptor&source=bl&ots=PmE6Zi5xWI&sig=ACfU3U3kutUDhLcV23sujT2ucVf9NTUXHg&hl=ru&sa=X&ved=2ahUKEwj8yb_d0cDiAhVBwqYKHX-UD1MQ6AEwCHoECAkQAQ#v=onepage&q=N-HYDROXY-3%2C4-METHYLENEDIOXYAMPHETAMINE%20receptor&f=false	Agonist 2678

PubMed

Title	Date	PubMed
Comparative potencies of 3,4-methylenedioxymethamphetamine (MDMA) analogues as inhibitors of [3H]noradrenaline and [3H]5-HT transport in mammalian cell lines.	2007 Dec	17891159
Degradation of N-hydroxy-3,4-methylenedioxymethamphetamine in aqueous solution and its prevention.	2009 Dec 15	19853392
Determination of a new designer drug, N-hydroxy-3,4-methylenedioxymethamphetamine and its metabolites in rats using ultra-performance liquid chromatography-tandem mass spectrometry.	2010 May 20	20299167

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 08:50:57 GMT 2023` Edited by `admin` on `Sat Dec 16 08:50:57 GMT 2023`
Record UNII	R0H604RFC0
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

MDOH hydrochloride

Common Name

English

1,3-BENZODIOXOLE-5-ETHANAMINE, N-HYDROXY-.ALPHA.-METHYL-, HYDROCHLORIDE

Systematic Name

English

MDH (PSYCHEDELIC) hydrochloride

Common Name

English

N-hydroxytenamphetamine hydrochloride

Common Name

English

N-HYDROXY MDA HYDROCHLORIDE [INCB GREEN LIST]

Common Name

English

3,4-Methylenedioxy-N-hydroxyamphetamine hydrochloride

Common Name

English

1-(1,3-BENZODIOXOL-5-YL)-N-HYDROXYPROPAN-2-AMINE HYDROCHLORIDE

Systematic Name

English

MDH hydrochloride

Common Name

English

N-HYDROXY MDA HYDROCHLORIDE

Common Name

English

N-HYDROXY-3,4-METHYLENEDIOXYAMPHETAMINE HYDROCHLORIDE

Systematic Name

English

Code System Code Type Description

CAS

74341-83-6