Compound Summary


  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 Dosage Unit CG Lifespan(AVG/MED days) TG Lifespan(AVG/MED days) Lifespan Change(AVG/MED%) CG Lifespan(MAX days) TG Lifespan(MAX days) Lifespan Change(MAX%) Significant Strain Gender PubMed Active Label
Caenorhabditis elegans 33 umol/L -13 NS N2 24134630 Inactive
  Experimental Data Visualization
 acetazolamide

  Statistics Data
 acetazolamide

Species Lifespan Change(AVG/MED%) Lifespan Change(MAX%) Count Reference Count Data point
Caenorhabditis elegans -13 1 1
  Statistics Data Visualization
 acetazolamide