(Z)-4-(Methoxycarbonylmethyl-methyl-amino)-3-phenyl-pent-2-enoic acid methyl ester; 1-(2-Benzhydrylideneaminooxy-ethyl)-1,2,5,6-tetrahydro-pyridine-3-carboxylic acid hydrochloride

ID: ALA540611

Chembl Id: CHEMBL540611

PubChem CID: 45265672

Max Phase: Preclinical

Molecular Formula: C37H44ClN3O7

Molecular Weight: 641.77

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  COC(=O)/C=C(/c1ccccc1)C(C)N(C)CC(=O)OC.Cl.O=C(O)C1=CCCN(CCON=C(c2ccccc2)c2ccccc2)C1

Standard InChI:  InChI=1S/C21H22N2O3.C16H21NO4.ClH/c24-21(25)19-12-7-13-23(16-19)14-15-26-22-20(17-8-3-1-4-9-17)18-10-5-2-6-11-18;1-12(17(2)11-16(19)21-4)14(10-15(18)20-3)13-8-6-5-7-9-13;/h1-6,8-12H,7,13-16H2,(H,24,25);5-10,12H,11H2,1-4H3;1H/b;14-10+;

Standard InChI Key:  NLSWVOSASINWAY-HWVPHXJSSA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 641.77

Molecular Weight (Monoisotopic): 641.3101

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References

1. Héja L, Kovács I, Szárics E, Incze M, Temesváriné-Major E, Dörnyei G, Peredy-Kajtár M, Gács-Baitz E, Szántay C, Kardos J..  (2004)  Novel secoergoline derivatives inhibit both GABA and glutamate uptake in rat brain homogenates: synthesis, in vitro pharmacology, and modeling.,  47  (23): [PMID:15509161] [10.1021/jm040809c]

Source

Source(1):

• Scientific Literature