ACDB Search

Compound Summary

acetazolamide

Compound Information

acetazolamide

Compound Name:	acetazolamide
Compound CID:	1986
Synonyms:	acetazolamide 59-66-5 Diamox N-(5-Sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide Acetazolamid More...
Iupac Name:	N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide
InChI:	InChI=1S/C4H6N4O3S2/c1-2(9)6-3-7-8-4(12-3)13(5,10)11/h1H3,(H2,5,10,11)(H,6,7,9)
InChIKey:	BZKPWHYZMXOIDC-UHFFFAOYSA-N
Canonical Smiles:	CC(=O)NC1=NN=C(S1)S(=O)(=O)N
Isomeric Smiles:	CC(=O)NC1=NN=C(S1)S(=O)(=O)N
Molecular Weight:	222.3
Molecular Formula:	C4H6N4O3S2

Compound Structure

2D Structure:

3D Structure:

Computed Properties

acetazolamide

Molecular Weight:	222.3
Molecular Formula:	C4H6N4O3S2
Hydrogen Bond Donor Count:	2
Hydrogen Bond Acceptor Count:	7
Rotatable Bond Count:	2
Heavy Atom Count:	13
Complexity:	297

Synonyms

acetazolamide

acetazolamide	acetazolamide
acetazolamide	59-66-5
Diamox	N-(5-Sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide
Acetazolamid	Acetamox
Diacarb	Glaupax
Defiltran	Nephramide
Cidamex	Diluran
Edemox	Dehydratin
Diuramid	Diutazol
Duiramid	Eumicton
Natrionex	Nephramid
Phonurit	Diakarb
Donmox	Fonurit
Glupax	Vetamox
Didoc	SK-acetazolamide
Diuriwas	5-Acetamido-1,3,4-thiadiazole-2-sulfonamide
Acetazoleamide	Acetozalamide
Diureticum-holzinger	Acetamidothiadiazolesulfonamide
Acetazolamida	Acetazolamidum
4-Diamox	Acetamide, N-5-(aminosulfonyl)-1,3,4-thiadiazol-2-yl-
Carbonic Anhydrase Inhibitor No. 6063	2-Acetylamino-1,3,4-thiadiazole-5-sulfonamide
N-5-(aminosulfonyl)-1,3,4-thiadiazol-2-ylacetamide	C4H6N4O3S2
2-Acetamido-5-sulfonamido-1,3,4-thiadiazole	Carbonic anhydrase inhibitor 6063
UNII-O3FX965V0I	NSC 145177
1,3,4-Thiadiazole-2-sulfonamide, 5-acetamido-	5-Acetamide-1,3,4-thiadiazole-2-sulfonamide
CHEMBL20	MFCD00003105
Diamox (TN)	N-(5-(Aminosulfonyl)-1,3,4-thiadiazol-2-yl)acetamide
MLS000028435	O3FX965V0I
CHEBI:27690	Acetamide, N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)-
NSC-145177	CAS-59-66-5
N-5-(Aminosulfonyl)-1,3,4-thiadiozol-2-yl-Acetamide	NCGC00015074-10
Acetazolamine	Acetamide, N-(5-(aminosulfonyl)-1,3,4-thiadiazol-2-yl)-
Atenezol	Glaumox
SMR000058394	Diamox Sequels
DSSTox_CID_2544	5-acetylamino-1,3,4-thiadiazole-2-sulfonamide
DSSTox_RID_76621	DSSTox_GSID_22544
Acetazolamidum INN-Latin	Acetazolamida INN-Spanish
N-(5-Aminosulfonyl-1,3,4-thiadiazol-2-yl)acetamide	N-5-(aminosulfonyl)-1,3,5-thiadiazol-2-ylacetamide
CCRIS 5811	Acetazolamide (AAZ)
HSDB 3002	SR-01000000065
EINECS 200-440-5	AI3-52458
Prestwick_4	1azm
1yda	1ydb
1ydd	1zsb
2xtk	3czv
3ucj	Acetazolamide, 5
Acetazolamide USP:INN:BAN:JAN	Acerazolamide, AAZ
Acetazolamide, AAZ	Acetazolamide, AZA
Acetazolamide, AZM	ACMC-20gwkd
Spectrum_000018	1jd0
2h4n	2uy4
3dc3	3hs4
3ml5	4g0c
Opera_ID_288	AZA2
Prestwick0_000003	Prestwick1_000003
Prestwick2_000003	Prestwick3_000003
Spectrum2_000082	Spectrum3_000284
Spectrum4_000139	Spectrum5_000738
Lopac-A-6011	A 6011
Lopac0_000039	SCHEMBL23219
BSPBio_000005	BSPBio_001788
KBioGR_000558	KBioSS_000358
MLS001148438	BIDD:GT0643
DivK1c_000017	SPECTRUM1500102
N-(5-Sulfamoyl-1,3,4thiadiazol-2-yl)-acetamide	SPBio_000004
SPBio_001926	BPBio1_000007
GTPL6792	(non-d)Acetazolamide-13C2-d3
Acetazolamide, >=99%, powder	DTXSID7022544
SCHEMBL11049053	BDBM10880
BZKPWHYZMXOIDC-UHFFFAOYSA-	HMS500A19
KBio1_000017	KBio2_000358
KBio2_002926	KBio2_005494
KBio3_001288	Acetazolamide (JP17/USP/INN)
AMY3289	Acetazolamide, analytical standard
NINDS_000017	HMS1568A07
HMS1920A05	HMS2091G05
HMS2095A07	HMS2232G23
HMS3259I13	HMS3260G19
HMS3370P01	HMS3712A07
HMS3744A21	Pharmakon1600-01500102
WLN: T5NN DSJ CSZW EMV1	ALBB-023617
BCP29616	EBD55026
HY-B0782	ZINC3813042
Tox21_110078	Tox21_201559
Tox21_302773	Tox21_500039
CCG-38900	NSC145177
NSC755854	s4506
SBB056640	AKOS000715163
Tox21_110078_1	CS-3568
DB00819	LP00039
MCULE-4029778803	NC00491
NSC-755854	SDCCGSBI-0050028.P005
Acetazolamide Related Compound (5-acetamido-1,3,4-thiadiazole-2-sulfonic acid)	IDI1_000017
NCGC00015074-01	NCGC00015074-02
NCGC00015074-03	NCGC00015074-04
NCGC00015074-05	NCGC00015074-06
NCGC00015074-07	NCGC00015074-08
NCGC00015074-09	NCGC00015074-11
NCGC00015074-12	NCGC00015074-14
NCGC00015074-15	NCGC00015074-17
NCGC00015074-22	NCGC00023455-03
NCGC00023455-04	NCGC00023455-05
NCGC00023455-06	NCGC00023455-07
NCGC00256374-01	NCGC00259108-01
NCGC00260724-01	AC-12779
AS-13169	H501
SBI-0050028.P004	2-Acetamido-5-sulfonamido-1,4-thiadiazole
5-Acetamide-1,4-thiadiazole-2-sulfonamide	DB-053437
5-Acetamido-1,3,4-thiadiazol-2-sulfonamide	AB00051906
EU-0100039	ST45022057
1,4-Thiadiazole-2-sulfonamide, 5-acetamido-	C06805
D00218	D88526
J10059	20506-EP2269989A1
20506-EP2275420A1	20506-EP2280008A2
20506-EP2295406A1	20506-EP2298772A1
20506-EP2308562A2	20506-EP2308839A1
20506-EP2314585A1	AB00051906_15
003A105	A832415
N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)ethanamide	Q413690
L 579486	Q-200579
Q-200580	SR-01000000065-2
SR-01000000065-4	SR-01000000065-6
BRD-K43457670-001-22-9	BRD-K43457670-001-26-0
Z277559108	Acetazolamide, European Pharmacopoeia (EP) Reference Standard
Acetazolamide, United States Pharmacopeia (USP) Reference Standard	N - (5 - Sulfamoyl - 1,3, 4 - thiadiazol - 2 - yl) acetamide
Acetazolamide for system suitability, European Pharmacopoeia (EP) Reference Standard	Acetazolamide, Pharmaceutical Secondary Standard; Certified Reference Material
124442-28-0	2-Acetamido-5-sulfamoyl-1,3,4-thiadiazole; 2-Acetylamino-1,3,4-thiadiazole-5-sulfonamide; 5-Acetamido-1,3,4-thiadiazole-2-sulfonamide

Experimental Data

acetazolamide

Species	Dose	Unit	Control(Avg days)	Treatment(Avg days)	Avg/Med Lifespan Change(%)	Control(Max days)	Treatment(Max days)	Max Lifespan Change(%)	Significant	Strain	Gender	PubMed	Avg/Med Lifespan Change tab
Caenorhabditis elegans	33.000000000000000	umol/L			-13.000000000000000				NS	N2		24134630	Inactive

Experimental Data Visualization

acetazolamide

Statistics Data

acetazolamide

Species	Avg/Med Lifespan Change(%)	Max Lifespan Change(%)	Count Reference	Count Data point
Caenorhabditis elegans	-13.000000000000000		1	1

Statistics Data Visualization

acetazolamide

Compound Name:

acetazolamide

Compound CID:

1986

Synonyms:

acetazolamide 59-66-5 Diamox N-(5-Sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide Acetazolamid More...

Iupac Name:

N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide

InChI:

InChI=1S/C4H6N4O3S2/c1-2(9)6-3-7-8-4(12-3)13(5,10)11/h1H3,(H2,5,10,11)(H,6,7,9)

InChIKey:

BZKPWHYZMXOIDC-UHFFFAOYSA-N

Canonical Smiles:

CC(=O)NC1=NN=C(S1)S(=O)(=O)N

Isomeric Smiles:

CC(=O)NC1=NN=C(S1)S(=O)(=O)N

Molecular Weight:

222.3

Molecular Formula:

C4H6N4O3S2

Molecular Weight:

222.3

Molecular Formula:

C4H6N4O3S2

Hydrogen Bond Donor Count:

2

Hydrogen Bond Acceptor Count:

7

Rotatable Bond Count:

2

Heavy Atom Count:

13

Complexity:

297

acetazolamide

59-66-5

Diamox

N-(5-Sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide

Acetazolamid

Acetamox

Diacarb

Glaupax

Defiltran

Nephramide

Cidamex

Diluran

Edemox

Dehydratin

Diuramid

Diutazol

Duiramid

Eumicton

Natrionex

Nephramid

Phonurit

Diakarb

Donmox

Fonurit

Glupax

Vetamox

Didoc

SK-acetazolamide

Diuriwas

5-Acetamido-1,3,4-thiadiazole-2-sulfonamide

Acetazoleamide

Acetozalamide

Diureticum-holzinger

Acetamidothiadiazolesulfonamide

Acetazolamida

Acetazolamidum

4-Diamox

Acetamide, N-5-(aminosulfonyl)-1,3,4-thiadiazol-2-yl-

Carbonic Anhydrase Inhibitor No. 6063

2-Acetylamino-1,3,4-thiadiazole-5-sulfonamide

N-5-(aminosulfonyl)-1,3,4-thiadiazol-2-ylacetamide

C4H6N4O3S2

2-Acetamido-5-sulfonamido-1,3,4-thiadiazole

Carbonic anhydrase inhibitor 6063

UNII-O3FX965V0I

NSC 145177

acetazolamide

59-66-5

Diamox

N-(5-Sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide

Acetazolamid

More...