ID: ALA3629730

Max Phase: Preclinical

Molecular Formula: C25H41N5O4S

Molecular Weight: 507.70

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC[C@H](C)[C@H](NC(=O)[C@H]1CCCCN1C)C(=O)N[C@H]1CCO[C@H](c2nc(C(=O)NC(C)C)cs2)C1

Standard InChI:  InChI=1S/C25H41N5O4S/c1-6-16(4)21(29-23(32)19-9-7-8-11-30(19)5)24(33)27-17-10-12-34-20(13-17)25-28-18(14-35-25)22(31)26-15(2)3/h14-17,19-21H,6-13H2,1-5H3,(H,26,31)(H,27,33)(H,29,32)/t16-,17-,19+,20-,21-/m0/s1

Standard InChI Key:  QEULMQYFEUMUMH-WJRACZLCSA-N

Associated Targets(non-human)

Tubulin 1327 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 507.70Molecular Weight (Monoisotopic): 507.2879AlogP: 2.63#Rotatable Bonds: 9
Polar Surface Area: 112.66Molecular Species: NEUTRALHBA: 7HBD: 3
#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.09CX Basic pKa: 7.09CX LogP: 1.81CX LogD: 1.63
Aromatic Rings: 1Heavy Atoms: 35QED Weighted: 0.47Np Likeness Score: -0.65

References

1. Park Y, Bae SY, Hah JM, Lee SK, Ryu JS..  (2015)  Synthesis of stereochemically diverse cyclic analogs of tubulysins.,  23  (21): [PMID:26474666] [10.1016/j.bmc.2015.10.003]

Source