Famotidine
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Description

Famotidine is a Histamine-2 Receptor Antagonist. The mechanism of action of famotidine is as a Histamine H2 Receptor Antagonist.

From NIH 3D

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Source creator
cass condray
Source license
CC-BY
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#nih-3d
#small molecules
#famotidine
#76824-35-6
#pepcid
#pepcid ac
#famodil
#gastridin
#pepcidine
#pepdine
#quamatel
#gaster
#pepdul
#famoxal
#ganor
#pepcidac
#amfamox
#gastropen
#famosan
#fluxid
#lecedil
#motiax
#muclox
#ym-11170
#pepcid rpd
#fadul
#mk-208
#famotidine (pepcid)
#3-[({2-[(diaminomethylidene)amino]-1,3-thiazol-4-yl}methyl)sulfanyl]-n-sulfamoylpropanimidamide
#l 643341
#mk 208
#chebi:4975
#ym 11170
#nsc-757810
#3-(((2-((diaminomethylene)amino)thiazol-4-yl)methyl)thio)-n'-sulfamoylpropanimidamide
#xufqphaneapemj-uhfffaoysa-
#3-(((2-guanidinothiazol-4-yl)methyl)thio)-n-sulfamoylpropanimidamide
#pepcid ac gelcaps
#smr000058961
#pepcid (tn)
#chembl902
#3-[[[2-[(aminoiminomethyl)amino]-4-thiazolyl]methyl]thio]-n-(aminosulfonyl)propanimidamide
#sr-05000001440
#5qzo15j2z8
#ncgc00015446-05
#fo9
#propanimidamide, n'-(aminosulfonyl)-3-(((2-((diaminomethylene)amino)-4-thiazolyl)methyl)thio)-
#prestwick_212
#cas-76824-35-6
#fluxid (tn)
#mfcd00079297
#hs-0054
#ym-1170
#famotidine [mi]
#3-(2-guanidinothiazol-4-ylmethylthio)-n1-sulfamoylpropionamide
#famotidine [inn]
#famotidine [jan]
#prestwick2_000104
#prestwick3_000104
#famotidine [hsdb]
#famotidine [usan]
#lopac-f-6889
#f0530
#schembl972
#schembl974
#famotidine [vandf]
#f 6889
#famotidine [mart.]
#famotidine [usp-rs]
#famotidine [who-dd]
#n'-(aminosulfonyl)-3-([2-(diaminomethyleneamino)-4-thiazolyl]methylthio)propanamidine
#lopac0_000497
#bspbio_000088
#mls000028583
#mls000758205
#mls001423994
#bidd:gt0759
#bpbio1_000098
#famotidine (jp17/usp/inn)
#famotidine [orange book]
#bdbm22891
#cid_5702160
#famotidine [ep monograph]
#famotidine [usp impurity]
#famotidine [usp monograph]
#hms1568e10
#hms2051a07
#hms2089i12
#hms2095e10
#hms2231i22
#hms3261d15
#hms3712e10
#hms3884j03
#hy-b0377
#tox21_500497
#bdbm50103514
#pdsp1_000398
#pdsp2_000396
#s2078
#stk527689
#akos005460541
#akos015994617
#ccg-100767
#ccg-220104
#ccg-221801
#nc00017
#sdccgsbi-0050481.p004
#3-[[2-(diaminomethylideneamino)-1,3-thiazol-4-yl]methylsulfanyl]-n'-sulfamoylpro
#propanimidamide, 3-[[[2-[aminoiminomethyl)amino]-4-thiazoyl]methyl]thio]-n-(aminosulfonyl)
#ncgc00015446-01
#ncgc00015446-02
#ncgc00015446-03
#ncgc00015446-04
#ncgc00015446-06
#ncgc00015446-08
#ncgc00018276-01
#ncgc00018276-02
#ncgc00093899-01
#ncgc00093899-02
#ncgc00093899-03
#ncgc00188952-01
#ncgc00261182-01
#(1z)-3-[({2-[(diaminomethylidene)amino]-1,3-thiazol-4-yl}methyl)sulfanyl]-n'-sulfamoylpropanimidamide
#(1z)-n'-(aminosulfonyl)-3-[({2-[(diaminomethylidene)amino]-1,3-thiazol-4-yl}methyl)thio]propanimidamide
#ac-11713
#ac-31723
#pepcid complete component famotidine
#sbi-0050481.p003
#eu-0100497
#famotidine component of pepcid complete
#d00318
#ab00383032_11
#824f356
#a838850
#a899959
#l003830
#l013386
#sr-01000075883
#sr-01000075883-1
#sr-05000001440-1
#sr-05000001440-2
#famotidine, british pharmacopoeia (bp) reference standard
#famotidine, european pharmacopoeia (ep) reference standard
#famotidine, united states pharmacopeia (usp) reference standard
#3-[(2-guanidinothiazol-4-yl)methylsulfanyl]-n-sulfamoyl-propanamidine
#famotidine, pharmaceutical secondary standard; certified reference material
#3-((((2-(diaminomethylene)amino)-4-thiazolyl)methyl)thio)-n-sulfamoylpropionamidine
#3-(2-(diaminomethyleneamino)-1,3-thiazol-4-yl)methylthio)-n'- sulfamoylpropionamidine
#3-[2-(diaminomethyleneamino] thiazol-4-ylmethylthio]-n-sulphamoyl propionamidine
#famotidine for system suitability, european pharmacopoeia (ep) reference standard
#3-[({2-[(diaminomethylene)amino]-1,3-thiazol-4-yl}methyl)sulfanyl]-n'-sulfamoylpropanimidamide
#3-[({2-[(diaminomethylidene)amino]-1,3-thiazol-4-yl}methyl)sulfanyl]-n''-sulfamoylpropanimidamide
#[1-amino-3-[[[2-[(diaminomethylene)amino]-4-thiazolyl]methyl]thio]propylidene]sulfamide
#en300-119506
#z1521553705
#3mf
#blend
#fbx
#glb
#jpg
#mtl
#obj
#ply
#png
#stl
#wrl
#x3d

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Famotidine

From NIH 3D
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Category

learning

License

CC-BY

Published

9/1/2026

Availability

free on NIH 3D