Standard InChI: InChI=1S/C18H27NO4/c1-4-5-6-7-8-11-14(19-12-9-10-13-19)15-16(20)22-18(2,3)23-17(15)21/h9-10H,4-8,11-13H2,1-3H3
Standard InChI Key: RTUQJLWWIKYVAW-UHFFFAOYSA-N
Associated Targets(non-human)
Oncopeltus fasciatus 71 Activities
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Aspergillus parasiticus 296 Activities
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Penicillium italicum 133 Activities
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Trichoderma viride 1263 Activities
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Phytophthora citrophthora 55 Activities
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Verticillium dahliae 119 Activities
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Alternaria alternata 757 Activities
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Trichothecium roseum 13 Activities
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Colletotrichum coccodes 59 Activities
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Colletotrichum gloeosporioides 560 Activities
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Geotrichum candidum 421 Activities
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Fusarium oxysporum f. sp. niveum 47 Activities
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Fusarium oxysporum f. sp. gladioli 10 Activities
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Fusarium culmorum 260 Activities
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Molecule Features
Natural Product: No
Oral: No
Chemical Probe: No
Parenteral: No
Molecule Type: Small molecule
Topical: No
First In Class: No
Black Box: No
Chirality: No
Availability: No
Prodrug: No
Drug Indications
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Properties
Molecular Weight: 321.42
Molecular Weight (Monoisotopic): 321.1940
AlogP: 3.31
#Rotatable Bonds: 7
Polar Surface Area: 55.84
Molecular Species: NEUTRAL
HBA: 5
HBD: 0
#RO5 Violations: 0
HBA (Lipinski): 5
HBD (Lipinski): 0
#RO5 Violations (Lipinski): 0
CX Acidic pKa:
CX Basic pKa:
CX LogP: 4.06
CX LogD: 4.06
Aromatic Rings: 0
Heavy Atoms: 23
QED Weighted: 0.24
Np Likeness Score: 0.30
References
1.Cantín A, Moya P, Miranda MA, Primo J, Primo-Yúfera E.. (2000) Synthesis and biological evaluation of new analogues of the active fungal metabolites N-(2-methyl-3-oxodecanoyl)-2-pyrroline and N-(2-methyl-3-oxodec-8-enoyl)-2-pyrroline (II)., 48 (8):[PMID:10956170][10.1021/jf990948g]