The Drug-Drug Interactions Ontology

Last uploaded: February 11, 2016
Preferred Name

metoclopramide

Synonyms

Elieten

4-amino-5-chloro-N-(2-(diethylamino)ethyl)-2-methoxybenzamide

2-methoxy-4-amino-5-chloro-N,N-(dimethylaminoethyl)benzamide

4-amino-5-chloro-N-(2-(diethylamino)ethyl)-o-anisamide

4-amino-5-chloro-2-methoxy-N-(beta-diethylaminoethyl)benzamide

2-methoxy-5-chloroprocainamide

metoclopramida

C14H22ClN3O2

metoclopramide

4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-methoxybenzamide

metoclopramidum

Reliveran

ID

http://purl.obolibrary.org/obo/CHEBI_107736

activates

http://purl.obolibrary.org/obo/dinto_3182

http://purl.obolibrary.org/obo/dinto_1051

AHFScode

56:32.00

altId

CHEBI:6898

ATCCode

A03FA01

blocks

http://purl.obolibrary.org/obo/dinto_2804

CASRN

364-62-5

DBBrand

meclopran

gastrobid

gastrotablinen

gastrotem

parmid

eucil

pramidin

gastro-timelets

mygdalon

paspertin

duraclamid

metoclopramide intensol

neu-sensamide

reliveran

apo-metoclop

pramin

pms-metoclopramide

emetid

terperan

maxeran

metoclopramide omega

gastrosil

elieten

peraprin

clopra

maxolon

metramid

emitasol

cerucal

del

metocobil

gastronerton

gastromax

emperal

nu-metoclopramide

octamide

primperan

imperan

pramiel

plasil

moriperan

reclomide

clopra-yellow

reglan

gastrese

metamide

clopromate

metoclol

DBname

metoclopramide

DBSynonym

methoclopramide

metaclopromide

metochlopramide

metaclopramide

metoclopramide hydrochloride

metoclopramidum [inn-latin]

metoclopramide hcl

methochlopramide

metoclopramida [inn-spanish]

Definition

Metoclopramide is a carboxamide resulting from the formal condensation of 4-amino-5-chloro-2-methoxybenzoic acid with the primary amino group of N,N-diethylethane-1,2-diamine.

has effect

http://purl.obolibrary.org/obo/OAE_0000355

http://purl.obolibrary.org/obo/OAE_0000411

http://purl.obolibrary.org/obo/OAE_0000770

http://purl.obolibrary.org/obo/OAE_0000309

http://purl.obolibrary.org/obo/OAE_0000377

http://purl.obolibrary.org/obo/OAE_0000690

http://purl.obolibrary.org/obo/OAE_0000677

http://purl.obolibrary.org/obo/OAE_0000218

http://purl.obolibrary.org/obo/OAE_0001001

http://purl.obolibrary.org/obo/OAE_0001129

http://purl.obolibrary.org/obo/OAE_0001437

http://purl.obolibrary.org/obo/OAE_0000391

http://purl.obolibrary.org/obo/OAE_0000300

http://purl.obolibrary.org/obo/OAE_0000268

http://purl.obolibrary.org/obo/OAE_0000500

http://purl.obolibrary.org/obo/OAE_0000592

http://purl.obolibrary.org/obo/OAE_0000468

http://purl.obolibrary.org/obo/OAE_0000512

http://purl.obolibrary.org/obo/OAE_0000780

http://purl.obolibrary.org/obo/OAE_0001297

http://purl.obolibrary.org/obo/OAE_0002206

http://purl.obolibrary.org/obo/OAE_0000365

http://purl.obolibrary.org/obo/OAE_0000376

http://purl.obolibrary.org/obo/OAE_0000275

http://purl.obolibrary.org/obo/OAE_0001217

http://purl.obolibrary.org/obo/OAE_0000921

http://purl.obolibrary.org/obo/OAE_0000403

http://purl.obolibrary.org/obo/OAE_0000034

http://purl.obolibrary.org/obo/OAE_0000021

http://purl.obolibrary.org/obo/OAE_0000310

http://purl.obolibrary.org/obo/OAE_0000166

http://purl.obolibrary.org/obo/OAE_0000388

http://purl.obolibrary.org/obo/OAE_0000584

http://purl.obolibrary.org/obo/OAE_0000779

http://purl.obolibrary.org/obo/OAE_0000362

http://purl.obolibrary.org/obo/OAE_0001309

http://purl.obolibrary.org/obo/OAE_0000551

has pharmacological target

http://purl.obolibrary.org/obo/dinto_3182

http://purl.obolibrary.org/obo/dinto_2804

has role

http://purl.obolibrary.org/obo/CHEBI_55324

http://purl.obolibrary.org/obo/CHEBI_50919

http://purl.obolibrary.org/obo/CHEBI_48561

InChI

InChI=1S/C14H22ClN3O2/c1-4-18(5-2)7-6-17-14(19)10-8-11(15)12(16)9-13(10)20-3/h8-9H,4-7,16H2,1-3H3,(H,17,19)

InChIKey

InChIKey=TTWJBBZEZQICBI-UHFFFAOYSA-N

induces

http://purl.obolibrary.org/obo/dinto_0278

inhibits

http://purl.obolibrary.org/obo/dinto_2667

http://purl.obolibrary.org/obo/dinto_2993

http://purl.obolibrary.org/obo/dinto_1559

is metabolised by

http://purl.obolibrary.org/obo/dinto_2993

label

metoclopramide

may interact with

http://purl.obolibrary.org/obo/CHEBI_15765

http://purl.obolibrary.org/obo/CHEBI_70707

http://purl.obolibrary.org/obo/CHEBI_9943

http://purl.obolibrary.org/obo/CHEBI_70735

http://purl.obolibrary.org/obo/CHEBI_61049

http://purl.obolibrary.org/obo/dinto_DB01267

http://purl.obolibrary.org/obo/CHEBI_51364

http://purl.obolibrary.org/obo/CHEBI_4031

http://purl.obolibrary.org/obo/CHEBI_9467

prefixIRI

obo2:CHEBI_107736

prefLabel

metoclopramide

SMILES

CCN(CC)CCNC(=O)c1cc(Cl)c(N)cc1OC

CCN(CC)CCNC(=O)C1=CC(Cl)=C(N)C=C1OC

Synonym

Elieten

4-amino-5-chloro-N-(2-(diethylamino)ethyl)-2-methoxybenzamide

2-methoxy-4-amino-5-chloro-N,N-(dimethylaminoethyl)benzamide

4-amino-5-chloro-N-(2-(diethylamino)ethyl)-o-anisamide

4-amino-5-chloro-2-methoxy-N-(beta-diethylaminoethyl)benzamide

2-methoxy-5-chloroprocainamide

metoclopramida

C14H22ClN3O2

metoclopramide

4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-methoxybenzamide

metoclopramidum

Reliveran

xref

KEGG DRUG:D00726

ChemSpider:4024

Drugs.com:http://www.drugs.com/metoclopramide.html

Reaxys:1884366

Wikipedia:http://en.wikipedia.org/wiki/Metoclopramide

Patent:BE620543

DrugBank:DB01233

PDRhealth:http://www.pdrhealth.com/drug_info/rxdrugprofiles/drugs/reg1369.shtml

RxList:http://www.rxlist.com/cgi/generic2/metoclo.htm

PharmGKB:PA450475

CASRN:364-62-5

PubChem Compound:4168

BindingDB:50000491

ChEBI:107736

Drugs Product Database (DPD):2243563

Guide To Pharmacology:241

National Drug Code Directory:0591-2228-05

Wikipedia:Metoclopramide

IUPHAR:241

PubChem Substance:46505631

Patent:US3177252

subClassOf

http://purl.obolibrary.org/obo/dinto_000055

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