MILDIOMYCIN

ID: ALA2287190

Max Phase: Preclinical

Molecular Formula: C19H32N8O9

Molecular Weight: 516.51

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  N=C(N)NCC(O)CC(O)(C(=O)O)[C@@H]1O[C@@H](N2C=C(CO)C(N)=NC2O)C=C[C@@H]1NC(=O)[C@@H](N)CO

Standard InChI:  InChI=1S/C19H32N8O9/c20-10(7-29)15(31)25-11-1-2-12(27-5-8(6-28)14(21)26-18(27)34)36-13(11)19(35,16(32)33)3-9(30)4-24-17(22)23/h1-2,5,9-13,18,28-30,34-35H,3-4,6-7,20H2,(H2,21,26)(H,25,31)(H,32,33)(H4,22,23,24)/t9?,10-,11-,12+,13+,18?,19?/m0/s1

Standard InChI Key:  AEVNGQKCBVULBP-YARLIKFLSA-N

Associated Targets(non-human)

Streptomyces alboniger 61 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Streptomyces acidiscabies 73 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Streptomyces scabiei 197 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: 516.51Molecular Weight (Monoisotopic): 516.2292AlogP: -6.05#Rotatable Bonds: 11
Polar Surface Area: 306.32Molecular Species: ZWITTERIONHBA: 13HBD: 12
#RO5 Violations: 3HBA (Lipinski): 17HBD (Lipinski): 15#RO5 Violations (Lipinski): 3
CX Acidic pKa: 3.60CX Basic pKa: 11.52CX LogP: -7.36CX LogD: -7.91
Aromatic Rings: 0Heavy Atoms: 36QED Weighted: 0.07Np Likeness Score: 0.99

References

1. NATSUME M, MATSUMOTO M, OHSHIRO A, KOZONE I, HASHIMOTO M, ABE H.  (2003)  Effect of Antibiotics on Formation of Aerial Mycelium and Production of Phytotoxins in Streptomyces spp.,  28  (2): [10.1584/jpestics.28.183]

Source