Benzolamide - Moligand™, ≥98% , Inhibitor of carbonic anhydrase 1;Inhibitor of carbonic anhydrase 12, CAS No.3368-13-6, Inhibitor of carbonic anhydrase 1;Inhibitor of carbonic anhydrase 12

CAS: 3368-13-6 Cat. No.: B607993 Formule: C8H8N4O4S3 Poids moléculaire: 320.37 PubChem CID: 18794
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
5-(benzenesulfonamido)-1,3,4-thiadiazole-2-sulfonamide|2-N-benzene-1,3,4-thiadiazole-2,5-disulfonamide|1,3,4-Thiadiazole-2-sulfonamide, 5-benzenesulfonamido-|2-benzenesulfonamido-1,3,4-thiadiazole-5-sulfonamide|D(+)-sucroseoctaacetate|2-(Phenylsulfonylamino)-1,3,4-thiadiazole-5-sulfonamide|5-(phenylsulfonamido)-1,3,4-thiadiazole-2-sulfonamide|CL 11366|W 1803|1,3,4-Thiadiazole-2-sulfonamide, 5-[(phenylsulfonyl)amino]-|1,3,4-Thiadiazole-2-sulfonamide, 5-((phenylsulfonyl)amino)-|5-(phenylsulfonylamino)-1,3,4-thiadiazole-2-sulfonamide|Benzolamide (BZA)|5-[(phenylsulfonyl)amino]-1,3,4-thiadiazole-2-sulfonamide|BZA1|BENZOLAMIDE
Storage
Store at 2-8°C,Protected from light
Shipped In
Wet ice
★
Taille
Allemagne (EU)
USA*
Prix
Qté
5mg
B607993-5mg
—
1 En stock
58,92€
10mg
B607993-10mg
—
1 En stock
88,42€
25mg
B607993-25mg
—
1 En stock
176,06€
50mg
B607993-50mg
—
1 En stock
279,33€
100mg
B607993-100mg
—
1 En stock
440,72€
Enter a quantity for the sizes you want to add.

Vue d’ensemble

Benzolamide (CL11366) is a potent carbonic anhydrase (CA) inhibitor, with Kis of 15 nM, 9 nM, 94 nM and 78 nM for hCA I, hCA II, EcoCAγ and VchCAγ, respectively. Benzolamide also inhibits CAS3, with a Ki of 54 nM. Benzolamide can be used for the research of glaucoma and seizures

Spécifications

Synonymes
5-(benzenesulfonamido)-1,3,4-thiadiazole-2-sulfonamide | 2-N-benzene-1,3,4-thiadiazole-2,5-disulfonamide | 1,3,4-Thiadiazole-2-sulfonamide, 5-benzenesulfonamido- | 2-benzenesulfonamido-1,3,4-thiadiazole-5-sulfonamide | D(+)-sucroseoctaacetate | 2-(Phenylsulfonylamino)-1,3,4-thiadiazole-5-sulfonamide | 5-(phenylsulfonamido)-1,3,4-thiadiazo Afficher plus
Spécifications et pureté
Moligand™, ≥98%
Conditions de stockage de stockage
Store at 2-8°C,Protected from light
Expédié en
Wet ice
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Grade
Moligand™
Type d'action
INHIBITOR
Mécanisme d'action
Inhibitor of carbonic anhydrase 1;Inhibitor of carbonic anhydrase 12
Pureté
≥98%
Noms et identifiants
Pubchem Sid
Sourires canoniques
C1=CC=C(C=C1)S(=O)(=O)NC2=NN=C(S2)S(=O)(=O)N
IUPAC Name
5-(benzenesulfonamido)-1,3,4-thiadiazole-2-sulfonamide
InChIKey
PWDGTQXZLNDOKS-UHFFFAOYSA-N
INCHI
1S/C8H8N4O4S3/c9-18(13,14)8-11-10-7(17-8)12-19(15,16)6-4-2-1-3-5-6/h1-5H,(H,10,12)(H2,9,13,14)
Isomères SMILES
C1=CC=C(C=C1)S(=O)(=O)NC2=NN=C(S2)S(=O)(=O)N
PubChem CID
18794
Poids moléculaire
320.37

Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassBenzenesulfonamides
Intermediate Tree Nodes Not available
Direct ParentBenzenesulfonamides
Alternative Parents Thiadiazole sulfonamides  Benzenesulfonyl compounds  Organosulfonamides  Heteroaromatic compounds  Aminosulfonyl compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Benzenesulfonamide - 1,3,4-thiadiazole-2-sulfonamide - Benzenesulfonyl group - Organosulfonic acid amide - Azole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Thiadiazole - Aminosulfonyl compound - Heteroaromatic compound - Organoheterocyclic compound - Azacycle - Organopnictogen compound - Organonitrogen compound - Organic oxygen compound - Organosulfur compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzenesulfonamides. These are organic compounds containing a sulfonamide group that is S-linked to a benzene ring.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
CA5A Tclin Carbonic anhydrase 5A, mitochondrial (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA5B Tclin Carbonic anhydrase 5B, mitochondrial (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA6 Tclin Carbonic anhydrase 6 (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA1 Tclin Carbonic anhydrase 1 (33 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA2 Tclin Carbonic anhydrase 2 (39 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA12 Tclin Carbonic anhydrase 12 (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA14 Tclin Carbonic anhydrase 14 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA9 Tclin Carbonic anhydrase 9 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA7 Tclin Carbonic anhydrase 7 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA3 Tclin Carbonic anhydrase III (753 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA6 Tclin Carbonic anhydrase VI (993 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase VB (957 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5A Tclin Carbonic anhydrase VA (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA2 Tclin Carbonic anhydrases; II & IX (262 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cibles associées (non humaines)
Ca7 Carbonic anhydrase VII (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca13 Carbonic anhydrase XIII (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Oryctolagus cuniculus (11301 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
cynT Carbonic anhydrase 1 (82 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca15 Carbonic anhydrase 15 (173 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
mtcA1 Uncharacterized protein Rv1284/MT1322 (182 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA Alpha carbonic anhydrase (93 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CAN2 Carbonic anhydrase 2 (140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Astrosclerin-3 (80 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ca1 Delta carbonic anhydrase (40 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
1272966 AGAP002992-PA (40 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase, alpha family (44 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot NumberCertificate TypeDateArticle
I2410356I2410356Certificate of AnalysisJul 25, 2024 B607993
I2410357I2410357Certificate of AnalysisJul 25, 2024 B607993
I2410358I2410358Certificate of AnalysisJul 25, 2024 B607993
I2410359I2410359Certificate of AnalysisJul 25, 2024 B607993
I2410360I2410360Certificate of AnalysisJul 25, 2024 B607993
I2410361I2410361Certificate of AnalysisJul 25, 2024 B607993
I2410362I2410362Certificate of AnalysisJul 25, 2024 B607993
I2410363I2410363Certificate of AnalysisJul 25, 2024 B607993
I2410364I2410364Certificate of AnalysisJul 25, 2024 B607993
I2410365I2410365Certificate of AnalysisJul 25, 2024 B607993
Propriétés chimiques et physiques
SolubilitéDMSO: 250 mg/mL (780.35 mM)
Sensibilitélight sensitive
Poids moléculaire320.400 g/mol
XLogP30.100
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count9
Rotatable Bond Count4
Exact Mass319.971 Da
Monoisotopic Mass319.971 Da
Topological Polar Surface Area177.000 Ų
Heavy Atom Count19
Formal Charge0
Complexity503.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQ et articles
Calculateurs de solution
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