Sepimostat - Moligand™,≥95% , CAS No.103926-64-3

CAS: 103926-64-3 Cat. No.: S413390 Formula: C₂₁H₁₉N₅O₂ Peso molecolare: 373.41

GRADE & PURITY Moligand™, ≥95%

Synonyms

SCHEMBL15535526 | Sepimostat [INN] | Q27263101 | HY-136299 | F81697 | (6-carbamimidoylnaphthalen-2-yl) 4-(4,5-dihydro-1H-imidazol-2-ylamino)benzoate | UNII-5ZFR16F4QQ | Sepimostat | 6-Carbamimidoylnaphthalen-2-yl 4-((4,5-dihydro-1H-imidazol-2-yl)amino)ben

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Panoramica

Information

Sepimostat (FUT-187 free base) is an inhibitor of Ifenprodil binding with Ki of 27.7  μM. Sepimostat is an antagonist of NR2B N-methyl-D-aspartate receptor acting at the Ifenprodil-binding site of the NR2B subunit with neuroprotective activity.

Specifications

Sinonimi

SCHEMBL15535526 | Sepimostat [INN] | Q27263101 | HY-136299 | F81697 | (6-carbamimidoylnaphthalen-2-yl) 4-(4,5-dihydro-1H-imidazol-2-ylamino)benzoate | UNII-5ZFR16F4QQ | Sepimostat | 6-Carbamimidoylnaphthalen-2-yl 4-((4,5-dihydro-1H-imidazol-2-yl)amino)ben

Specifiche e purezza

Moligand™,≥95%

Meccanismi biochimici e fisiologici

Sepimostat (FUT-187 free base) is an inhibitor of Ifenprodil binding with Ki of 27.7\u2009 μM. Sepimostat is an antagonist of NR2B N-methyl-D-aspartate receptor acting at the Ifenprodil-binding site of the NR2B subunit with neuroprotective activity.

Condizioni di conservazione di stoccaggio

Protected from light,Store at -20°C,Argon charged

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Moligand™

Tipo di azione

ANTAGONIST

Purezza

≥95%

Nomi e identificatori

• Sorrisi canonici: C1CN=C(N1)NC2=CC=C(C=C2)C(=O)OC3=CC4=C(C=C3)C=C(C=C4)C(=N)N
• IUPAC Name: (6-carbamimidoylnaphthalen-2-yl) 4-(4,5-dihydro-1H-imidazol-2-ylamino)benzoate
• InChIKey: QMRJOIUGPCVZPH-UHFFFAOYSA-N
• INCHI: 1S/C21H19N5O2/c22-19(23)16-2-1-15-12-18(8-5-14(15)11-16)28-20(27)13-3-6-17(7-4-13)26-21-24-9-10-25-21/h1-8,11-12H,9-10H2,(H3,22,23)(H2,24,25,26)
• Isomeri SMILES: C1CN=C(N1)NC2=CC=C(C=C2)C(=O)OC3=CC4=C(C=C3)C=C(C=C4)C(=N)N
• Peso molecolare: 373.41

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Naphthalenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Naphthalenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Naphthalenes
• Alternative Parents: Benzoic acid esters Aniline and substituted anilines Imidazolyl carboxylic acids and derivatives Benzoyl derivatives Imidazolines Guanidines Carboxylic acid esters Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Monocarboxylic acids and derivatives Carboximidamides Carboxamidines Hydrocarbon derivatives Organic oxides Organooxygen compounds Organopnictogen compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Benzoate ester - Naphthalene - Benzoic acid or derivatives - Benzoyl - Aniline or substituted anilines - Imidazolyl carboxylic acid derivative - Monocyclic benzene moiety - 2-imidazoline - Carboxylic acid ester - Guanidine - Amidine - Carboxylic acid amidine - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic oxygen compound - Organopnictogen compound - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
• 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

Obiettivi associati (umani)

F12 Tchem Coagulation factor XII (1 Activities)

Discover Target: F12

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Obiettivi associati (non umani)

Trypsin (394 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: Light sensitive
• Peso molecolare: 373.400 g/mol
• XLogP3: 2.200
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 373.154 Da
• Monoisotopic Mass: 373.154 Da
• Topological Polar Surface Area: 113.000 Ų
• Heavy Atom Count: 28
• Formal Charge: 0
• Complexity: 614.000
• 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