Butazolamide , CAS No.16790-49-1

CAS: 16790-49-1 Cat. No.: B668303 Formule: C6H10N4O3S2 Poids moléculaire: 250.3 PubChem CID: 519309
DISPONIBLE À COMMANDE
Synonyms
Butazolamide|N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)butanamide|N-(5-Sulfamoyl-1,3,4-thiadiazol-2-yl)butyramide|SKF 4965|Butamide; SKF 4965|Butyramide, N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)-|2-m-Butyrylamino-1,3,4-thiadiazole-5-sulfonamide|Butanamide, N-(5-(aminosulfonyl)-1,3,4-thiadiazol-2-yl)-|5-butyramido-2-sulfamoyl-1,3,4-thiadiazole|VFJ|BUTAZOLAMIDE [MI]
Storage
Room temperature
★
Taille
USA
Allemagne (EU)*
Prix
Qté
1mg
B668303-1mg
Sur commande · 8–12 semaines

571,90$US

857,90$US
Enregistrer 286,00 $US (33.34%)
5mg
B668303-5mg
Sur commande · 8–12 semaines

1 999,90$US

2 999,90$US
Enregistrer 1 000,00 $US (33.33%)
Enter a quantity for the sizes you want to add.

Spécifications

Synonymes
Butazolamide | N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)butanamide | N-(5-Sulfamoyl-1,3,4-thiadiazol-2-yl)butyramide | SKF 4965 | Butamide; SKF 4965 | Butyramide, N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)- | 2-m-Butyrylamino-1,3,4-thiadiazole-5-sulfonamide | Butanamide, N-(5-(aminosulfonyl)-1,3,4-thiadiazol-2-yl)- | 5-butyramido-2-sulfamoyl-1,3,4 Afficher plus
Conditions de stockage de stockage
Room temperature
Propriétés du produit
ALogP
0.6
Noms et identifiants
Sourires canoniques
CCCC(=O)NC1=NN=C(S1)S(=O)(=O)N
IUPAC Name
N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)butanamide
InChIKey
HZIYHIRJHYIRQO-UHFFFAOYSA-N
INCHI
1S/C6H10N4O3S2/c1-2-3-4(11)8-5-9-10-6(14-5)15(7,12)13/h2-3H2,1H3,(H2,7,12,13)(H,8,9,11)
Isomères SMILES
CCCC(=O)NC1=NN=C(S1)S(=O)(=O)N
PubChem CID
519309
Poids moléculaire
250.3

Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasseAzoles
SubclassThiadiazoles
Intermediate Tree Nodes Not available
Direct ParentThiadiazole sulfonamides
Alternative Parents N-arylamides  Organosulfonamides  Fatty amides  Heteroaromatic compounds  Aminosulfonyl compounds  Secondary carboxylic acid amides  Azacyclic compounds  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 1,3,4-thiadiazole-2-sulfonamide - N-arylamide - Fatty amide - Organosulfonic acid amide - Fatty acyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Heteroaromatic compound - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as thiadiazole sulfonamides. These are heterocyclic compounds containing a thiazole ring substituted by at least one sulfonamide group.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
CA1 Tclin Carbonic anhydrase 1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA2 Tclin Carbonic anhydrase 2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA4 Tclin Carbonic anhydrase 4 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA9 Tclin Carbonic anhydrase 9 (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
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cibles associées (non humaines)
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus faecium (13803 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:
Propriétés chimiques et physiques
Poids moléculaire250.300 g/mol
XLogP30.600
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count4
Exact Mass250.019 Da
Monoisotopic Mass250.019 Da
Topological Polar Surface Area152.000 Ų
Heavy Atom Count15
Formal Charge0
Complexity326.000
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
Calculateurs de solution
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