BUTRIPTYLINE

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NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C21H27N
Molecular Weight	293.4458
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of BUTRIPTYLINE

Structure Search

SMILES

CC(CC1C2=CC=CC=C2CCC3=CC=CC=C13)CN(C)C

InChI

InChIKey=ALELTFCQZDXAMQ-UHFFFAOYSA-N

InChI=1S/C21H27N/c1-16(15-22(2)3)14-21-19-10-6-4-8-17(19)12-13-18-9-5-7-11-20(18)21/h4-11,16,21H,12-15H2,1-3H3

HIDE SMILES / InChI

Molecular Formula	C21H27N
Molecular Weight	293.4458
Charge	0
Count

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

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 16:09:21 UTC 2023` Edited by `admin` on `Fri Dec 15 16:09:21 UTC 2023`
Record UNII	Z22441975X
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

BUTRIPTYLINE

Official Name

English

(±)-10,11-DIHYDRO-N,N,.BETA.-TRIMETHYL-5H-DIBENZO(A,D)CYCLOHEPTENE-5-PROPYLAMINE

Systematic Name

English

5H-DIBENZO(A,D)CYCLOHEPTENE-5-PROPANAMINE, 10,11-DIHYDRO-N,N,.BETA.-TRIMETHYL-, (±)-

Systematic Name

English

BUTRIPTYLINE [MI]

Common Name

English

butriptyline [INN]

Common Name

English

Butriptyline [WHO-DD]

Common Name

English

EVADYNE

Brand Name

English

Classification Tree Code System Code

WHO-VATC

QN06AA15

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

NCI_THESAURUS

C265

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

WHO-ATC

N06AA15

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

Code System Code Type Description

PUBCHEM

21772

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

PRIMARY

RXCUI

19895

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

PRIMARY

RxNorm

SMS_ID

100000076906

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

PRIMARY

DRUG BANK

DB09016

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

PRIMARY

EVMPD

SUB13137MIG

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

PRIMARY

FDA UNII

Z22441975X

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

PRIMARY

CAS

35941-65-2

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

PRIMARY

NCI_THESAURUS

C79855

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

PRIMARY

DRUG CENTRAL

455

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

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MERCK INDEX

m2805

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

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Merck Index

INN

2123

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

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WIKIPEDIA

BUTRIPTYLINE

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

PRIMARY

ChEMBL

CHEMBL2110816

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

PRIMARY

EPA CompTox

DTXSID6022715

Created by admin on Fri Dec 15 16:09:21 UTC 2023 , Edited by admin on Fri Dec 15 16:09:21 UTC 2023

PRIMARY

Related Record Type Details


					OE8026NXVX

BUTRIPTYLINE, (S)-

ENANTIOMER -> RACEMATE


					NQI5D806LC

5-HYDROXYTRYPTAMINE RECEPTOR 2A

TARGET -> INHIBITOR


					LIJ2H8658W

BUTRIPTYLINE HYDROCHLORIDE

SALT/SOLVATE -> PARENT


					U3CV8K30PO

BUTRIPTYLINE, (R)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					Z22441975X

ACTIVE MOIETY