ID: ALA4645875

Max Phase: Preclinical

Molecular Formula: C37H47Br2N7O5

Molecular Weight: 829.63

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1ccccc1C1CCN(C(=O)N[C@H](Cc2cc(Br)c(O)c(Br)c2)C(=O)N[C@@H](CCCCN)C(=O)N2CCN(c3ccncc3)CC2)CC1

Standard InChI:  InChI=1S/C37H47Br2N7O5/c1-51-33-8-3-2-6-28(33)26-11-16-46(17-12-26)37(50)43-32(24-25-22-29(38)34(47)30(39)23-25)35(48)42-31(7-4-5-13-40)36(49)45-20-18-44(19-21-45)27-9-14-41-15-10-27/h2-3,6,8-10,14-15,22-23,26,31-32,47H,4-5,7,11-13,16-21,24,40H2,1H3,(H,42,48)(H,43,50)/t31-,32+/m0/s1

Standard InChI Key:  CVPWNBYUSUFFDB-AJQTZOPKSA-N

Associated Targets(Human)

Calcitonin-gene-related peptide receptor, CALCRL/RAMP1 193 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 829.63Molecular Weight (Monoisotopic): 827.2005AlogP: 4.78#Rotatable Bonds: 13
Polar Surface Area: 153.36Molecular Species: BASEHBA: 8HBD: 4
#RO5 Violations: 1HBA (Lipinski): 12HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: 6.75CX Basic pKa: 10.20CX LogP: 2.82CX LogD: 2.08
Aromatic Rings: 3Heavy Atoms: 51QED Weighted: 0.18Np Likeness Score: -0.57

References

1. Dubowchik GM, Conway CM, Xin AW..  (2020)  Blocking the CGRP Pathway for Acute and Preventive Treatment of Migraine: The Evolution of Success.,  63  (13): [PMID:32058712] [10.1021/acs.jmedchem.9b01810]

Source