(+)-Hydantocidin

ID: ALA2285997

Chembl Id: CHEMBL2285997

Cas Number: 130607-26-0

PubChem CID: 125429

Max Phase: Preclinical

Molecular Formula: C7H10N2O6

Molecular Weight: 218.16

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C1NC(=O)[C@@]2(N1)O[C@H](CO)[C@@H](O)[C@H]2O

Standard InChI:  InChI=1S/C7H10N2O6/c10-1-2-3(11)4(12)7(15-2)5(13)8-6(14)9-7/h2-4,10-12H,1H2,(H2,8,9,13,14)/t2-,3-,4-,7+/m1/s1

Standard InChI Key:  RFZZKBWDDKMWNM-GTBMBKLPSA-N

Alternative Forms

  1. Parent:

    ALA2285997

    HYDANTOCIDIN

Associated Targets(non-human)

Eleusine indica (140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ambrosia artemisiifolia (23 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Xanthium strumarium (250 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Digitaria sanguinalis (1594 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Solanum nigrum (20 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Echinochloa crus-galli (3685 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ipomoea purpurea (35 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Abutilon theophrasti (831 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Panicum dichotomiflorum (12 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Setaria viridis (435 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sorghum halepense (127 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: 218.16Molecular Weight (Monoisotopic): 218.0539AlogP: -3.36#Rotatable Bonds: 1
Polar Surface Area: 128.12Molecular Species: NEUTRALHBA: 6HBD: 5
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.21CX Basic pKa: CX LogP: -2.70CX LogD: -2.76
Aromatic Rings: 0Heavy Atoms: 15QED Weighted: 0.29Np Likeness Score: 2.03

References

1. Sano H, Mio S, Tsukaguchi N, Sugai S.  (1995)  Stereocontrolled synthesis of spirosuccinimide derivative of (+)-hydantocidin,  51  (5): [10.1016/0040-4020(94)01027-W]
2. Sano H, Mio S, Kitagawa J, Shindou M, Honma T, Sugai S.  (1995)  Synthesis of spirothiohydantoin analogues of hydantocidin,  51  (46): [10.1016/0040-4020(95)00810-U]

Source