Tecovirimat - 10mM in DMSO , Envelope phospholipase F13 (p37) inhibitor, CAS No.869572-92-9, Envelope phospholipase F13 (p37) inhibitor

CAS: 869572-92-9 Cat. No.: T426515 Formule: C₁₉H₁₅F₃N₂O₃ Poids moléculaire: 376.33 Numéro CE: 188-175-0 PubChem CID: 16124688

GRADE & PURITY 10mM in DMSO

Synonyms

AKOS030260536 | MFCD29047086 | Benzamide, N-[(3aR,4R,4aR,5aS,6S,6aS)-3,3a,4,4a,5,5a,6,6a-octahydro-1,3-dioxo-4,6-ethenocycloprop[f]isoindol-2(1H)-yl]-4-(trifluoromethyl)-, rel- | SIGA-246 | J05AX24 | SCHEMBL2360460 | 4-trifluoromethyl-N-(3,3a,4,4a,5,5a,6,

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Vue d’ensemble

Information

Tecovirimat Tecovirimat (Arestvyr, SIGA-246, ST-246, TPOXX) is an antiviral that inhibits the egress of orthopoxviruses by targeting viral p37 protein orthologs . Tecovirimat is developed for the treatment of smallpox infection.

Targets

p37 protein ortholog

Specifications

Synonymes

AKOS030260536 | MFCD29047086 | Benzamide, N-[(3aR,4R,4aR,5aS,6S,6aS)-3,3a,4,4a,5,5a,6,6a-octahydro-1,3-dioxo-4,6-ethenocycloprop[f]isoindol-2(1H)-yl]-4-(trifluoromethyl)-, rel- | SIGA-246 | J05AX24 | SCHEMBL2360460 | 4-trifluoromethyl-N-(3,3a,4,4a,5,5a,6,

Spécifications et pureté

10mM in DMSO

Mécanismes biochimiques et physiologiques

Tecovirimat (Arestvyr, SIGA-246, ST-246, TPOXX) is an antiviral that inhibits the egress of orthopoxviruses by targeting viral p37 protein orthologs. Tecovirimat is developed for the treatment of smallpox infection.

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.

Type d'action

INHIBITOR

Mécanisme d'action

Envelope phospholipase F13 (p37) inhibitor

Propriétés du produit

• ALogP: 2.018
• Nombre de HBD: 1
• Liaison rotative: 3

Noms et identifiants

• Pubchem Sid: 528767470
• Sourires canoniques: C1C2C1C3C=CC2C4C3C(=O)N(C4=O)NC(=O)C5=CC=C(C=C5)C(F)(F)F
• IUPAC Name: N-[(1S,2S,6R,7R,8R,10S)-3,5-dioxo-4-azatetracyclo[5.3.2.02,6.08,10]dodec-11-en-4-yl]-4-(trifluoromethyl)benzamide
• InChIKey: CSKDFZIMJXRJGH-VWLPUNTISA-N
• INCHI: 1S/C19H15F3N2O3/c20-19(21,22)9-3-1-8(2-4-9)16(25)23-24-17(26)14-10-5-6-11(13-7-12(10)13)15(14)18(24)27/h1-6,10-15H,7H2,(H,23,25)/t10-,11+,12+,13-,14-,15+
• Isomères SMILES: C1[C@@H]2[C@H]1[C@@H]3C=C[C@H]2[C@@H]4[C@H]3C(=O)N(C4=O)NC(=O)C5=CC=C(C=C5)C(F)(F)F
• PubChem CID: 16124688
• Poids moléculaire: 376.33

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Isoindoles and derivatives
      • Subclass Isoindolines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Isoindoles and derivatives
• Subclass: Isoindolines
• Intermediate Tree Nodes: Not available
• Direct Parent: Isoindolones
• Alternative Parents: Trifluoromethylbenzenes Benzoic acids and derivatives Benzoyl derivatives Pyrrolidine-2-ones Dicarboximides Lactams Carboxylic acid hydrazides Azacyclic compounds Organonitrogen compounds Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl fluorides
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Trifluoromethylbenzene - Isoindolone - Benzoic acid or derivatives - Benzoyl - Monocyclic benzene moiety - Benzenoid - 2-pyrrolidone - Pyrrolidone - Pyrrolidine - Dicarboximide - Carboxylic acid hydrazide - Lactam - Carboxylic acid derivative - Azacycle - Alkyl fluoride - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone.
• 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

Cibles associées (humaines)

Homo sapiens (32628 Activities)

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HFF (3142 Activities)

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Hdac6 Histone deacetylase 6 (222 Activities)

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Monkeypox virus (80 Activities)

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Mus musculus (284745 Activities)

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Cowpox virus (428 Activities)

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Vaccinia virus (4609 Activities)

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Variola virus (134 Activities)

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Human immunodeficiency virus 1 (70413 Activities)

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Vero (26788 Activities)

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Cynomolgus monkey (4946 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Camelpox virus (273 Activities)

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Ectromelia virus Moscow (12 Activities)

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Vaccinia virus WR (86 Activities)

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8238086 Cytochrome P450 (0 Activities)

Discover Target: 8238086

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OPG057 Envelope phospholipase F13 (p37) (19 Activities)

Discover Target: OPG057

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SARS-CoV-2 (38078 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• DMSO (mg/mL) Solubilité maximale: 75
• DMSO (mM) Solubilité maximale: 199.293173544496
• Eau (mg/mL) Solubilité maximale: ＜1
• Poids moléculaire: 376.300 g/mol
• XLogP3: 2.600
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 376.103 Da
• Monoisotopic Mass: 376.103 Da
• Topological Polar Surface Area: 66.500 Ų
• Heavy Atom Count: 27
• Formal Charge: 0
• Complexity: 705.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 6
• 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