ID: ALA4466914

Max Phase: Preclinical

Molecular Formula: C32H36Br2F4N6O4

Molecular Weight: 644.67

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C[N+](C)(CC#CCOC1=NOCC1)Cc1cc(F)c(/N=N/c2c(F)cc(C[N+](C)(C)CC#CCOC3=NOCC3)cc2F)c(F)c1.[Br-].[Br-]

Standard InChI:  InChI=1S/C32H36F4N6O4.2BrH/c1-41(2,11-5-7-13-43-29-9-15-45-39-29)21-23-17-25(33)31(26(34)18-23)37-38-32-27(35)19-24(20-28(32)36)22-42(3,4)12-6-8-14-44-30-10-16-46-40-30;;/h17-20H,9-16,21-22H2,1-4H3;2*1H/q+2;;/p-2/b38-37+;;

Standard InChI Key:  JGURFMYKGKJPFD-XPPIURIRSA-L

Associated Targets(Human)

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Chrm1 Muscarinic acetylcholine receptor (3770 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: 644.67Molecular Weight (Monoisotopic): 644.2723AlogP: 5.32#Rotatable Bonds: 10
Polar Surface Area: 86.36Molecular Species: NEUTRALHBA: 8HBD: 0
#RO5 Violations: 2HBA (Lipinski): 10HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.34CX Basic pKa: 0.69CX LogP: -2.46CX LogD: -2.46
Aromatic Rings: 2Heavy Atoms: 46QED Weighted: 0.15Np Likeness Score: -0.23

References

1. Agnetta L, Bermudez M, Riefolo F, Matera C, Claro E, Messerer R, Littmann T, Wolber G, Holzgrabe U, Decker M..  (2019)  Fluorination of Photoswitchable Muscarinic Agonists Tunes Receptor Pharmacology and Photochromic Properties.,  62  (6): [PMID:30827105] [10.1021/acs.jmedchem.8b01822]

Source