ID: ALA2273063

Max Phase: Preclinical

Molecular Formula: C16H11ClN4S2

Molecular Weight: 358.88

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Clc1ccccc1-c1nnc(SCc2nc3ccccc3[nH]2)s1

Standard InChI:  InChI=1S/C16H11ClN4S2/c17-11-6-2-1-5-10(11)15-20-21-16(23-15)22-9-14-18-12-7-3-4-8-13(12)19-14/h1-8H,9H2,(H,18,19)

Standard InChI Key:  OEMANPJRSRINLH-UHFFFAOYSA-N

Associated Targets(non-human)

Sagittaria latifolia 66 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Schoenoplectus acutus 66 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Echinochloa crus-galli 3685 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Oryza sativa 2923 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Abutilon theophrasti 831 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Convolvulaceae 72 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Avena sativa 212 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Spodoptera litura 1708 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Culex pipiens pallens 759 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Tetranychus cinnabarinus 1124 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Musca domestica 713 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Rhizoctonia solani 2251 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Helminthosporium 185 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: 358.88Molecular Weight (Monoisotopic): 358.0114AlogP: 5.03#Rotatable Bonds: 4
Polar Surface Area: 54.46Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 11.58CX Basic pKa: 5.15CX LogP: 4.46CX LogD: 4.46
Aromatic Rings: 4Heavy Atoms: 23QED Weighted: 0.52Np Likeness Score: -2.31

References

1. Mishra L, Singh VK, Dubey NK, Mishra AK..  (1993)  Synthesis and fungicidal activity of some 5-membered heterocyclic derivatives containing benzimidazoles.,  57  (6): [PMID:7763889] [10.1271/bbb.57.989]

Source