Dazmegrel , CAS No.76894-77-4

CAS: 76894-77-4 Cat. No.: D667912 Formula: C16H17N3O2 Peso molecolare: 283.32 PubChem CID: 53555
Disponibile su ordine
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
★
Dimensione
Germania (EU)
USA*
Prezzo
Qtà
1mg
D667912-1mg
Su ordinazione · 8–12 settimane

496,26€

744,43€
Salva 248,17 € (33.34%)
5mg
D667912-5mg
Su ordinazione · 8–12 settimane

1.735,39€

2.603,13€
Salva 867,74 € (33.33%)
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Specifiche

Sinonimi
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 Mostra altro
Condizioni di conservazione di stoccaggio
Room temperature
Tipo di azione
INHIBITOR
Proprietà del prodotto
ALogP
1.5
Nomi e identificatori
Sorrisi canonici
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)
Isomeri SMILES
CC1=C(C2=CC=CC=C2N1CCC(=O)O)CN3C=CN=C3
PubChem CID
53555
Peso molecolare
283.32

Dati avanzati

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasseIndoles 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
DescrizioneThis 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
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
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
Obiettivi associati (non umani)
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
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
Peso molecolare283.320 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
Calcolatori di soluzioni
Recensioni

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