4''-deoxy-4''-Aminoavermectin derivative

ID: ALA274531

Chembl Id: CHEMBL274531

PubChem CID: 44460514

Max Phase: Preclinical

Molecular Formula: C50H75NO15

Molecular Weight: 930.14

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCC(C)[C@H]1O[C@]2(C=C[C@@H]1C)C[C@@H]1C[C@@H](C/C=C(\C)[C@@H](O[C@H]3C[C@H](OC)[C@@H](O[C@H]4C[C@H](OC)[C@H](NC(=O)OC)[C@H](C)O4)[C@H](C)O3)[C@@H](C)/C=C/C=C3\CO[C@@H]4[C@H](O)C(C)=C[C@@H](C(=O)O1)[C@]34O)O2

Standard InChI:  InChI=1S/C50H75NO15/c1-12-26(2)44-29(5)18-19-49(66-44)24-35-21-34(65-49)17-16-28(4)43(27(3)14-13-15-33-25-59-46-42(52)30(6)20-36(47(53)62-35)50(33,46)55)63-40-23-38(57-10)45(32(8)61-40)64-39-22-37(56-9)41(31(7)60-39)51-48(54)58-11/h13-16,18-20,26-27,29,31-32,34-46,52,55H,12,17,21-25H2,1-11H3,(H,51,54)/b14-13+,28-16+,33-15+/t26?,27-,29-,31-,32-,34+,35-,36-,37-,38-,39-,40-,41+,42+,43-,44+,45-,46+,49+,50+/m0/s1

Standard InChI Key:  XMWIOPLGIHIWNN-NUXPRJNTSA-N

Associated Targets(non-human)

Artemia (698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Haemonchus contortus (724 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Teladorsagia circumcincta (67 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichostrongylus axei (45 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichostrongylus colubriformis (210 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cooperia (29 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cooperia oncophora (36 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Oesophagostomum columbianum (45 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

Calculated Properties

Molecular Weight: 930.14Molecular Weight (Monoisotopic): 929.5137AlogP: 5.74#Rotatable Bonds: 9
Polar Surface Area: 188.16Molecular Species: NEUTRALHBA: 15HBD: 3
#RO5 Violations: 3HBA (Lipinski): 16HBD (Lipinski): 3#RO5 Violations (Lipinski): 3
CX Acidic pKa: 12.52CX Basic pKa: CX LogP: 6.18CX LogD: 6.18
Aromatic Rings: 0Heavy Atoms: 66QED Weighted: 0.19Np Likeness Score: 2.08

References

1. Mrozik H, Eskola P, Arison BH, Linn BO, Lusi A, Matzuk A, Shih TL, Tischler M, Waksmunski FS, Wyvratt MJ, Blizzard TA, Margiatto GM, Fisher MH, Shoop WL, Egerton JR.  (1995)  4-Deoxy-4-aminoavermectins with potent broad spectrum antiparasitic activities,  (20): [10.1016/0960-894X(95)00424-R]

Source