monactin

ID: ALA300034

Chembl Id: CHEMBL300034

PubChem CID: 44293442

Max Phase: Preclinical

Molecular Formula: C41H66O12

Molecular Weight: 750.97

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Synonyms: Monactin | Monactin|CHEMBL300034

Canonical SMILES:  CC[C@H]1C[C@@H]2CC[C@@H](O2)[C@@H](C)C(=O)O[C@H](C)C[C@H]2CC[C@H](O2)[C@H](C)C(=O)O[C@@H](C)C[C@@H]2CC[C@@H](O2)[C@@H](C)C(=O)O[C@H](C)C[C@H]2CC[C@H](O2)[C@H](C)C(=O)O1

Standard InChI:  InChI=1S/C41H66O12/c1-9-29-21-33-13-17-36(52-33)27(7)40(44)48-23(3)19-31-11-15-34(50-31)25(5)38(42)46-22(2)18-30-10-14-35(49-30)26(6)39(43)47-24(4)20-32-12-16-37(51-32)28(8)41(45)53-29/h22-37H,9-21H2,1-8H3/t22-,23+,24+,25-,26+,27+,28-,29-,30-,31+,32+,33-,34-,35+,36+,37-/m0/s1

Standard InChI Key:  YPUPRVWRYDPGCW-GGOMOPATSA-N

Alternative Forms

  1. Parent:

    ALA300034

    MONACTIN

Associated Targets(Human)

A2058 (690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A2780 (11979 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: 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: 750.97Molecular Weight (Monoisotopic): 750.4554AlogP: 6.41#Rotatable Bonds: 1
Polar Surface Area: 142.12Molecular Species: NEUTRALHBA: 12HBD: 0
#RO5 Violations: 3HBA (Lipinski): 12HBD (Lipinski): 0#RO5 Violations (Lipinski): 3
CX Acidic pKa: CX Basic pKa: CX LogP: 5.96CX LogD: 5.96
Aromatic Rings: 0Heavy Atoms: 53QED Weighted: 0.22Np Likeness Score: 0.61

References

1. Lee JW, Priestley ND..  (1998)  A free energy calculation can be used to predict K(+)-binding constants for new macrotetrolide antibiotics.,  (13): [PMID:9873423] [10.1016/s0960-894x(98)00300-x]
2. Harinantenaina Rakotondraibe L, Rasolomampianina R, Park HY, Li J, Slebodnik C, Brodie PJ, Blasiak LC, Hill R, TenDyke K, Shen Y, Cassera MB, Rejo F, Kingston DG..  (2015)  Antiproliferative and antiplasmodial compounds from selected Streptomyces species.,  25  (23): [PMID:26508548] [10.1016/j.bmcl.2015.07.103]

Source