ID: ALA326060

Max Phase: Preclinical

Molecular Formula: C30H51N3O9

Molecular Weight: 597.75

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCC(C)[C@H]1C(=O)O[C@H](C)C(=O)N(C)[C@@H](C(C)CC)C(=O)O[C@H](C)C(=O)N(C)[C@@H](C(C)CC)C(=O)O[C@H](C)C(=O)N1C

Standard InChI:  InChI=1S/C30H51N3O9/c1-13-16(4)22-28(37)40-20(8)26(35)32(11)24(18(6)15-3)30(39)42-21(9)27(36)33(12)23(17(5)14-2)29(38)41-19(7)25(34)31(22)10/h16-24H,13-15H2,1-12H3/t16?,17?,18?,19-,20-,21-,22+,23+,24+/m1/s1

Standard InChI Key:  ZZQUTSJAJOEJOG-SJGHBNOSSA-N

Associated Targets(non-human)

Ovis aries 854 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: 597.75Molecular Weight (Monoisotopic): 597.3625AlogP: 2.41#Rotatable Bonds: 6
Polar Surface Area: 139.83Molecular Species: NEUTRALHBA: 9HBD: 0
#RO5 Violations: 1HBA (Lipinski): 12HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 3.64CX LogD: 3.64
Aromatic Rings: 0Heavy Atoms: 42QED Weighted: 0.33Np Likeness Score: 0.55

References

1. Jeschke P, Benet-Buchholz J, Harder A, Etzel W, Schindler M, Thielking G..  (2003)  Synthesis and anthelmintic activity of cyclohexadepsipeptides with (S,S,S,R,S,R)-configuration.,  13  (19): [PMID:12951110] [10.1016/s0960-894x(03)00688-7]

Source