ID: ALA4797189

Max Phase: Preclinical

Molecular Formula: C21H17N3O5S

Molecular Weight: 423.45

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  N[C@@H]1CN(C(=O)c2csc3c(O)c4c(c(O)c23)C(=O)c2ccccc2C4=O)C[C@H]1N

Standard InChI:  InChI=1S/C21H17N3O5S/c22-11-5-24(6-12(11)23)21(29)10-7-30-20-13(10)18(27)14-15(19(20)28)17(26)9-4-2-1-3-8(9)16(14)25/h1-4,7,11-12,27-28H,5-6,22-23H2/t11-,12-/m1/s1

Standard InChI Key:  TWFGQEVTQGCUET-VXGBXAGGSA-N

Associated Targets(Human)

CAPAN-1 772 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HCT-116 91556 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

NCI-H460 60772 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HL-60 67320 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

K562 73714 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

TERT-RPE1 415 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: 423.45Molecular Weight (Monoisotopic): 423.0889AlogP: 1.20#Rotatable Bonds: 1
Polar Surface Area: 146.95Molecular Species: BASEHBA: 8HBD: 4
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 6#RO5 Violations (Lipinski): 1
CX Acidic pKa: 7.08CX Basic pKa: 8.92CX LogP: 1.19CX LogD: 1.20
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.34Np Likeness Score: -0.12

References

1. Tikhomirov AS,Litvinova VA,Andreeva DV,Tsvetkov VB,Dezhenkova LG,Volodina YL,Kaluzhny DN,Treshalin ID,Schols D,Ramonova AA,Moisenovich MM,Shtil AA,Shchekotikhin AE.  (2020)  Amides of pyrrole- and thiophene-fused anthraquinone derivatives: A role of the heterocyclic core in antitumor properties.,  199  [PMID:32428792] [10.1016/j.ejmech.2020.112294]

Source