Sulfacetamide - Moligand™, 10mM in DMSO , CAS No.144-80-9

CAS: 144-80-9 Cat. No.: S421650 Formule: C₈H₁₀N₂O₃S Poids moléculaire: 214.24 Beilstein Registry Number: 981718 Numéro CE: 205-640-6 PubChem CID: 5320

QUALITÉ & PURETÉ Moligand™, 10mM in DMSO

Synonyms

sulfacetamide|144-80-9|Sulphacetamide|Acetosulfamine|N-((4-Aminophenyl)sulfonyl)acetamide|N-Acetylsulfanilamide|N-Sulfanilylacetamide|Acetosulfamin|Albucid|Urosulfon|N-Sulphanilylacetamide|Sulfacetimide|Acetocid|Sulfacet|Sulfanilacetamide|Formosulfacetami

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Spécifications

Synonymes

sulfacetamide | 144-80-9 | Sulphacetamide | Acetosulfamine | N-((4-Aminophenyl)sulfonyl)acetamide | N-Acetylsulfanilamide | N-Sulfanilylacetamide | Acetosulfamin | Albucid | Urosulfon | N-Sulphanilylacetamide | Sulfacetimide | Acetocid | Sulfacet | Sulfanilacetamide | Formosulfacetami

Spécifications et pureté

Moligand™, 10mM in DMSO

Conditions de stockage de stockage

Store at -80°C

Expédié en

Dry ice packs + Cold packs

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Moligand™

Propriétés du produit

ALogP

-1

Noms et identifiants

Pubchem Sid

528774421

Sourires canoniques

CC(=O)NS(=O)(=O)C1=CC=C(C=C1)N

IUPAC Name

N-(4-aminophenyl)sulfonylacetamide

InChIKey

SKIVFJLNDNKQPD-UHFFFAOYSA-N

INCHI

1S/C8H10N2O3S/c1-6(11)10-14(12,13)8-4-2-7(9)3-5-8/h2-5H,9H2,1H3,(H,10,11)

Isomères SMILES

CC(=O)NS(=O)(=O)C1=CC=C(C=C1)N

WGK Allemagne

2

RTECS

AC8450000

PubChem CID

5320

Poids moléculaire

214.24

Beilstein

981718

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzenesulfonamides

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Benzenesulfonamides
• Intermediate Tree Nodes: Not available
• Direct Parent: Aminobenzenesulfonamides
• Alternative Parents: Benzenesulfonyl compounds Aniline and substituted anilines Organosulfonic acids and derivatives Aminosulfonyl compounds Acetamides Amino acids and derivatives Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Aminobenzenesulfonamide - Benzenesulfonyl group - Aniline or substituted anilines - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Acetamide - Aminosulfonyl compound - Amino acid or derivatives - Carboxylic acid derivative - Organic oxide - Organopnictogen compound - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Amine - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as aminobenzenesulfonamides. These are organic compounds containing a benzenesulfonamide moiety with an amine group attached to the benzene ring.
• External Descriptors: substituted aniline - sulfonamide

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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DHFR Tclin Dihydrofolate reductase (3072 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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PGR Tclin Progesterone receptor (8562 Activities)

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ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

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HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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DRD2 Tclin Dopamine D2 receptor (23596 Activities)

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GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)

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TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

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MAOA Tclin Monoamine oxidase A (11911 Activities)

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CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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HRH2 Tclin Histamine H2 receptor (5428 Activities)

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AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)

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HRH1 Tclin Histamine H1 receptor (7573 Activities)

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OPRM1 Tclin Mu opioid receptor (19785 Activities)

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DRD3 Tclin Dopamine D3 receptor (14368 Activities)

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AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

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OPRD1 Tclin Delta opioid receptor (15096 Activities)

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OPRK1 Tclin Kappa opioid receptor (16155 Activities)

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HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)

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SLC6A3 Tclin Dopamine transporter (10535 Activities)

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GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)

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KCNH2 Tclin HERG (29587 Activities)

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ADORA3 Tchem Adenosine A3 receptor (15931 Activities)

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BDKRB2 Tclin Bradykinin B2 receptor (3970 Activities)

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Mc4r Melanocortin receptor 4 (1205 Activities)

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Cckar Cholecystokinin A receptor (90 Activities)

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Pde4d Phosphodiesterase 4D (4 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• Point de fusion (°C): 179-184°C
• Poids moléculaire: 214.240 g/mol
• XLogP3: -1.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 214.041 Da
• Monoisotopic Mass: 214.041 Da
• Topological Polar Surface Area: 97.600 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 299.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1