Dazmegrel , CAS No.76894-77-4

CAS: 76894-77-4 Cat. No.: D667912 Fórmula: C16H17N3O2 Peso molecular: 283.32 PubChem CID: 53555
Disponible para pedir
Synonyms
DAZMEGREL|UK-38485|UK-38,485|3-(Imidazol-1-ylmethyl)-2-methylindole-1-propionic acid|1H-Indole-1-propanoic acid, 3-(1H-imidazol-1-ylmethyl)-2-methyl-|1H-Indole-1-propanoicacid, 3-(1H-imidazol-1-ylmethyl)-2-methyl-|Dazmegrelum [Latin]|Dazmegrelum|UK 38,485|Dazmegrel [USAN:INN:BAN]|DAZMEGREL [INN]|3-[3-(imidazol-1-ylmethyl)-2-methylindol-1-yl]propanoic acid|Dazmegrel (USAN/INN)|DAZMEGREL [USAN]|DAZMEGREL [MART.]|3-(3-Imidazol-1-ylmethyl-2-methyl-indol-1-yl)-propionic acid|3-[3-(1H-imidazol-1-ylmethyl)-2-methyl-1H-indol-1-yl]propanoic acid
Storage
Room temperature
★
Talla
Alemania (EU)
USA*
Precio
Cantidad
1mg
D667912-1mg
Fabricado bajo pedido · 8–12 semanas

496,26€

744,43€
Guardar 248,17 € (33.34%)
5mg
D667912-5mg
Fabricado bajo pedido · 8–12 semanas

1.735,39€

2.603,13€
Guardar 867,74 € (33.33%)
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Especificaciones

Sinónimos
DAZMEGREL | UK-38485 | UK-38,485 | 3-(Imidazol-1-ylmethyl)-2-methylindole-1-propionic acid | 1H-Indole-1-propanoic acid, 3-(1H-imidazol-1-ylmethyl)-2-methyl- | 1H-Indole-1-propanoicacid, 3-(1H-imidazol-1-ylmethyl)-2-methyl- | Dazmegrelum [Latin] | Dazmegrelum | UK 38,485 | Dazmegrel [USAN:INN:BAN] | DAZMEGREL [INN] | 3-[3-(imidazol-1-ylme Show more
Condiciones de almacenamiento de almacenamiento
Room temperature
Tipo de acción
INHIBITOR
Propiedades del producto
ALogP
1.5
Nombres e identificadores
Sonrisas canónicas
CC1=C(C2=CC=CC=C2N1CCC(=O)O)CN3C=CN=C3
IUPAC Name
3-[3-(imidazol-1-ylmethyl)-2-methylindol-1-yl]propanoic acid
InChIKey
DEQLGSOHGTZKFB-UHFFFAOYSA-N
INCHI
1S/C16H17N3O2/c1-12-14(10-18-9-7-17-11-18)13-4-2-3-5-15(13)19(12)8-6-16(20)21/h2-5,7,9,11H,6,8,10H2,1H3,(H,20,21)
Isómeros SMILES
CC1=C(C2=CC=CC=C2N1CCC(=O)O)CN3C=CN=C3
PubChem CID
53555
Peso molecular
283.32

Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseIndoles and derivatives
SubclassIndolyl carboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentIndolyl carboxylic acids and derivatives
Alternative Parents N-alkylindoles  3-alkylindoles  Imidazolyl carboxylic acids and derivatives  Substituted pyrroles  N-substituted imidazoles  Benzenoids  Heteroaromatic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Indolyl carboxylic acid derivative - N-alkylindole - 3-alkylindole - Indole - Imidazolyl carboxylic acid derivative - N-substituted imidazole - Substituted pyrrole - Benzenoid - Azole - Imidazole - Pyrrole - Heteroaromatic compound - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Azacycle - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as indolyl carboxylic acids and derivatives. These are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
TBXAS1 Tchem Thromboxane-A synthase (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP11B1 Tclin Cytochrome P450 11B1 (1750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXAS1 Tchem Thromboxane-A synthase (3355 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGIS Tchem Prostaglandin I2 synthase (104 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PMP22 Tbio Peripheral myelin protein 22 (699 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ptgs1 Prostaglandin G/H synthase (cyclooxygenase) (169 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
Peso molecular283.320 g/mol
XLogP31.500
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Exact Mass283.132 Da
Monoisotopic Mass283.132 Da
Topological Polar Surface Area60.100 Ų
Heavy Atom Count21
Formal Charge0
Complexity377.000
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
Calculadoras de soluciones
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