Butazolamide , CAS No.16790-49-1

CAS: 16790-49-1 Cat. No.: B668303 Formula: C6H10N4O3S2 Peso molecolare: 250.3 PubChem CID: 519309
Disponibile su ordine
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
★
Dimensione
Germania (EU)
USA*
Prezzo
Qtà
1mg
B668303-1mg
Su ordinazione · 8–12 settimane

496,26€

744,43€
Salva 248,17 € (33.34%)
5mg
B668303-5mg
Su ordinazione · 8–12 settimane

1.735,39€

2.603,13€
Salva 867,74 € (33.33%)
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Specifiche

Sinonimi
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 Mostra altro
Condizioni di conservazione di stoccaggio
Room temperature
Proprietà del prodotto
ALogP
0.6
Nomi e identificatori
Sorrisi canonici
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)
Isomeri SMILES
CCCC(=O)NC1=NN=C(S1)S(=O)(=O)N
PubChem CID
519309
Peso molecolare
250.3

Dati avanzati

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
DescrizioneThis 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
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
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
Obiettivi associati (non umani)
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus faecium (13803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
Peso molecolare250.300 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
Calcolatori di soluzioni
Recensioni

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