The Drug-Drug Interactions Ontology

Last uploaded: February 11, 2016
Preferred Name

amoxicillin
Synonyms

amoxicillinum

(2S,5R,6R)-6-[(2R)-2-amino-2-(4-hydroxyphenyl)acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

AMPC

amoxicillin

Amolin

Amopenixin

Clamoxyl

amoxycillin

amoxicilline

6-(p-hydroxy-alpha-aminophenylacetamido)penicillanic acid

alpha-amino-p-hydroxybenzylpenicillin

Amoxicillin

Moxal

AX

amoxicilina

Amoxicillin anhydrous

(2S,5R,6R)-6-{[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

6beta-[(2R)-2-amino-2-(4-hydroxyphenyl)acetamido]-2,2-dimethylpenam-3alpha-carboxylic acid

p-hydroxyampicillin

C16H19N3O5S

ID

http://purl.obolibrary.org/obo/CHEBI_2676

AHFScode

08:12.16.08

altId

CHEBI:133770

ATCCode

J01CA04

binds

http://purl.obolibrary.org/obo/dinto_4015

http://purl.obolibrary.org/obo/dinto_4065

http://purl.obolibrary.org/obo/dinto_2004

http://purl.obolibrary.org/obo/dinto_0520

http://purl.obolibrary.org/obo/dinto_0291

CASRN

26787-78-0

DBBrand

trimox

polymox

zimox

histocillin

amoxiden

amolin

delacillin

ospamox

unicillin

dispermox

ampc

clamoxyl

cemoxin

metafarma capsules

amoxil

metifarma capsules

utimox

pamoxicillin

lamoxy

amoxi

amoxi-mast

aspenil

hiconcil

amopen

piramox

tolodina

actimoxi

moxal

moxacin

amoxivet

amoxibiotic

flemoxin

vetramox

sumox

amopenixin

efpenix

ibiamox

robamox

sawamox pm

bristamox

anemolin

wymox

biomox

amoclen

imacillin

DBname

amoxicillin

DBSynonym

amoxicillin trihydrate

amoxicillin anhydrous

amoxicilline [inn-french]

amoxycillin

amoxicillinum [inn-latin]

amoxicilina [inn-spanish]

amoxycillin trihydrate

d-amoxicillin

p-hydroxyampicillin

Definition

A penicillin in which the substituent at position 6 of the penam ring is a 2-amino-2-(4-hydroxyphenyl)acetamido group.

has effect

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

http://purl.obolibrary.org/obo/OAE_0000449

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

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

http://purl.obolibrary.org/obo/OAE_0000492

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

http://purl.obolibrary.org/obo/OAE_0000308

http://purl.obolibrary.org/obo/OAE_0000210

http://purl.obolibrary.org/obo/OAE_0001448

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

http://purl.obolibrary.org/obo/OAE_0000600

http://purl.obolibrary.org/obo/OAE_0000920

http://purl.obolibrary.org/obo/OAE_0000103

http://purl.obolibrary.org/obo/OAE_0000601

http://purl.obolibrary.org/obo/OAE_0001463

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

http://purl.obolibrary.org/obo/OAE_0000455

http://purl.obolibrary.org/obo/OAE_0000498

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

http://purl.obolibrary.org/obo/OAE_0000086

http://purl.obolibrary.org/obo/OAE_0000645

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

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

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

http://purl.obolibrary.org/obo/OAE_0001106

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

http://purl.obolibrary.org/obo/OAE_0000866

http://purl.obolibrary.org/obo/OAE_0000306

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

http://purl.obolibrary.org/obo/OAE_0000487

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

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

http://purl.obolibrary.org/obo/OAE_0000565

http://purl.obolibrary.org/obo/OAE_0000374

http://purl.obolibrary.org/obo/OAE_0001366

http://purl.obolibrary.org/obo/OAE_0000480

http://purl.obolibrary.org/obo/OAE_0000402

http://purl.obolibrary.org/obo/OAE_0000811

has pharmacological target

http://purl.obolibrary.org/obo/dinto_4015

has role

http://purl.obolibrary.org/obo/CHEBI_36047

InChI

InChI=1S/C16H19N3O5S/c1-16(2)11(15(23)24)19-13(22)10(14(19)25-16)18-12(21)9(17)7-3-5-8(20)6-4-7/h3-6,9-11,14,20H,17H2,1-2H3,(H,18,21)(H,23,24)/t9-,10-,11+,14-/m1/s1

InChIKey

InChIKey=LSQZJLSUYDQPKJ-NJBDSQKTSA-N

inhibits

http://purl.obolibrary.org/obo/dinto_4015

http://purl.obolibrary.org/obo/dinto_4065

http://purl.obolibrary.org/obo/dinto_2004

http://purl.obolibrary.org/obo/dinto_0520

is metabolised by

http://purl.obolibrary.org/obo/dinto_0291

is substrate of

http://purl.obolibrary.org/obo/dinto_0291

label

amoxicillin

may interact with

http://purl.obolibrary.org/obo/CHEBI_44185

http://purl.obolibrary.org/obo/CHEBI_63334

http://purl.obolibrary.org/obo/CHEBI_50845

http://purl.obolibrary.org/obo/dinto_DB01357

http://purl.obolibrary.org/obo/CHEBI_27701

http://purl.obolibrary.org/obo/CHEBI_6805

http://purl.obolibrary.org/obo/CHEBI_27902

http://purl.obolibrary.org/obo/dinto_DB00977

http://purl.obolibrary.org/obo/CHEBI_50694

http://purl.obolibrary.org/obo/CHEBI_4392

prefixIRI

obo2:CHEBI_2676

prefLabel

amoxicillin

SMILES

[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)[C@H](N)C1=CC=C(O)C=C1)C(O)=O

[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)[C@H](N)c1ccc(O)cc1)C(O)=O

Synonym

amoxicillinum

(2S,5R,6R)-6-[(2R)-2-amino-2-(4-hydroxyphenyl)acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

AMPC

amoxicillin

Amolin

Amopenixin

Clamoxyl

amoxycillin

amoxicilline

6-(p-hydroxy-alpha-aminophenylacetamido)penicillanic acid

alpha-amino-p-hydroxybenzylpenicillin

Amoxicillin

Moxal

AX

amoxicilina

Amoxicillin anhydrous

(2S,5R,6R)-6-{[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

6beta-[(2R)-2-amino-2-(4-hydroxyphenyl)acetamido]-2,2-dimethylpenam-3alpha-carboxylic acid

p-hydroxyampicillin

C16H19N3O5S

xref

KEGG DRUG:D07452

ChEBI:2676

Reaxys:4274654

CiteXplore:12833570

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

RxList:http://www.rxlist.com/cgi/generic/amox.htm

PharmGKB:PA448406

Patent:DE1942693

CiteXplore:11906332

KEGG COMPOUND:C06827

Patent:US3192198

PubChem Substance:46507578

CiteXplore:16033609

PubChem Compound:33613

ChEMBL:243284

CASRN:26787-78-0

Patent:GB978178

DrugBank:DB01060

CiteXplore:10930630

CiteXplore:12569987

Drugs Product Database (DPD):2262886

National Drug Code Directory:0781-6039-58

CiteXplore:2083978

CiteXplore:11431418

Beilstein:4274654

Wikipedia:Amoxicillin

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

Patent:GB1241844

CiteXplore:12850488

ChemSpider:31006

subClassOf

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

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