ID: ALA4873018

Max Phase: Preclinical

Molecular Formula: C26H33N3O3

Molecular Weight: 435.57

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC12CCC3(CN(c4ccccc4)C(=O)C3C1C(=O)N/N=C1\C[C@H]3CC[C@]1(C)C3(C)C)O2

Standard InChI:  InChI=1S/C26H33N3O3/c1-23(2)16-10-11-24(23,3)18(14-16)27-28-21(30)19-20-22(31)29(17-8-6-5-7-9-17)15-26(20)13-12-25(19,4)32-26/h5-9,16,19-20H,10-15H2,1-4H3,(H,28,30)/b27-18+/t16-,19?,20?,24+,25?,26?/m1/s1

Standard InChI Key:  KIZRCDRYPDBNJI-XGPAGNRCSA-N

Associated Targets(Human)

HEK-293T 167025 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

MDCK 10148 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Orthohantavirus hantanense 22 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Vesicular stomatitis virus 4460 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: 435.57Molecular Weight (Monoisotopic): 435.2522AlogP: 3.91#Rotatable Bonds: 3
Polar Surface Area: 71.00Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.80CX Basic pKa: 1.54CX LogP: 3.34CX LogD: 3.34
Aromatic Rings: 1Heavy Atoms: 32QED Weighted: 0.73Np Likeness Score: 0.43

References

1. Yarovaya OI, Kovaleva KS, Zaykovskaya AA, Yashina LN, Scherbakova NS, Scherbakov DN, Borisevich SS, Zubkov FI, Antonova AS, Peshkov RY, Eltsov IV, Pyankov OV, Maksyutov RA, Salakhutdinov NF..  (2021)  New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazonesv.,  40  [PMID:33705902] [10.1016/j.bmcl.2021.127926]

Source