Pasiniazid - 10mM in DMSO , CAS No.2066-89-9

CAS: 2066-89-9 Cat. No.: P422509 Summenformel: C₆H₇N₃O · C₇H₇NO₃ Molekulargewicht: 290.27 EG-Nummer: 218-183-2 PubChem CID: 16367

GRADE & PURITY 10mM in DMSO

Synonyms

UNII-83J17CN0MN | PASINIAZID [INN] | IDI1_000327 | NCGC00024460-02 | Pharmakon1600-01503381 | AKOS026749897 | NCGC00021150-02 | NCGC00024460-03 | Isonicotinic acid hydrazide, mono(4-aminosalicylate) | SCHEMBL865578 | BSPBio_002450 | 4-amino-2-hydroxy-benz

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

Product Describtion:

Pasiniazid is an anti-TB and anti-leprosy drug, used to treat various types of TB and leprosy.

Specifications

Synonyme

UNII-83J17CN0MN | PASINIAZID [INN] | IDI1_000327 | NCGC00024460-02 | Pharmakon1600-01503381 | AKOS026749897 | NCGC00021150-02 | NCGC00024460-03 | Isonicotinic acid hydrazide, mono(4-aminosalicylate) | SCHEMBL865578 | BSPBio_002450 | 4-amino-2-hydroxy-benz

Spezifikationen & Reinheit

10mM in DMSO

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Aktionsart

INHIBITOR

Namen und Kennungen

• Pubchem Sid: 528766737
• Kanonisches Lächeln: C1=CC(=C(C=C1N)O)C(=O)O.C1=CN=CC=C1C(=O)NN
• IUPAC Name: 4-amino-2-hydroxybenzoic acid;pyridine-4-carbohydrazide
• InChIKey: RKPHTRVPGYGVQD-UHFFFAOYSA-N
• INCHI: 1S/C7H7NO3.C6H7N3O/c8-4-1-2-5(7(10)11)6(9)3-4;7-9-6(10)5-1-3-8-4-2-5/h1-3,9H,8H2,(H,10,11);1-4H,7H2,(H,9,10)
• Isomere SMILES: C1=CC(=C(C=C1N)O)C(=O)O.C1=CN=CC=C1C(=O)NN
• PubChem CID: 16367
• Molekulargewicht: 290.27

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Benzene and substituted derivatives
      • Subclass Benzoic acids and derivatives
        • Ebene5 Hydroxybenzoic acid derivatives
          • Ebene6 Salicylic acid and derivatives
            • Ebene7 Aminosalicylic acids and derivatives
              • Ebene8 Aminosalicylic acids

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Benzene and substituted derivatives
• Subclass: Benzoic acids and derivatives
• Intermediate Tree Nodes: Hydroxybenzoic acid derivatives - Salicylic acid and derivatives - Aminosalicylic acids and derivatives
• Direct Parent: Aminosalicylic acids
• Alternative Parents: 4-aminosalicylic acids Salicylic acids Aminobenzoic acids Pyridinecarboxylic acids and derivatives Benzoic acids m-Aminophenols Aniline and substituted anilines Benzoyl derivatives 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Vinylogous acids Heteroaromatic compounds Carboxylic acid hydrazides Amino acids Monocarboxylic acids and derivatives Azacyclic compounds Carboxylic acids Hydrocarbon derivatives Organic oxides Organooxygen compounds Organopnictogen compounds Primary amines
• Molecular Framework: Not available
• Substituents: 4-aminosalicylic acid - Aminosalicylic acid - Aminobenzoic acid - Aminobenzoic acid or derivatives - Salicylic acid - Benzoic acid - Pyridine carboxylic acid or derivatives - M-aminophenol - Aminophenol - Benzoyl - Aniline or substituted anilines - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Pyridine - Heteroaromatic compound - Vinylogous acid - Amino acid or derivatives - Amino acid - Carboxylic acid hydrazide - Organoheterocyclic compound - Azacycle - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Primary amine - Aromatic heteromonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as aminosalicylic acids. These are salicylic acids carrying an amino group on the benzene ring.
• External Descriptors: Not available

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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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)

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Mapt Microtubule-associated protein tau (6 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Molekulargewicht: 290.270 g/mol
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 2
• Exact Mass: 290.102 Da
• Monoisotopic Mass: 290.102 Da
• Topological Polar Surface Area: 152.000 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 280.000
• 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: 2

XLogP3