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Name |
botryospyrone D
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Molecular Formula | C13H16O5 | |
IUPAC Name* |
4-hydroxy-6,8-dimethoxy-3,7-dimethyl-3,4-dihydroisochromen-1-one
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|
SMILES |
COc1cc2c(c(OC)c1C)C(=O)OC(C)C2O
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InChI |
InChI=1S/C13H16O5/c1-6-9(16-3)5-8-10(12(6)17-4)13(15)18-7(2)11(8)14/h5,7,11,14H,1-4H3/t7-,11-/m0/s1
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InChIKey |
VNZFGBOMNXGPEV-CPCISQLKSA-N
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Synonyms |
NA
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CAS | NA | |
PubChem CID | NA | |
ChEMBL ID | NA |
Chemical Classification: |
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Endophyte ID | Endophyte Name | Family | Genus | Taxonomy ID | GenBank ID | Closest GenBank ID | Reference | |
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Endophyte ID | Endophyte Name | Family | Genus | Taxonomy ID | GenBank ID | Closest GenBank ID | Reference |
Bioactivity Name | Target ID | Target Name | Target Type | Target Organism | Target Organism ID | Potency of Bioactivity | Activity Type | Value | Unit | Endophyte ID | Endophyte Name | |
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Bioactivity Name | Target ID | Target Name | Target Type | Target Organism | Target Organism ID | Potency of Bioactivity | Activity Type | Value | Unit | Endophyte ID | Endophyte Name |
Molecular Weight: | 252.27 | ALogp: | 1.6 |
HBD: | 1 | HBA: | 5 |
Rotatable Bonds: | 2 | Lipinski's rule of five: | Accepted |
Polar Surface Area: | 65.0 | Aromatic Rings: | 2 |
Heavy Atoms: | 18 | QED Weighted: | 0.817 |
Caco-2 Permeability: | -4.726 | MDCK Permeability: | 0.00002170 |
Pgp-inhibitor: | 0.001 | Pgp-substrate: | 0.013 |
Human Intestinal Absorption (HIA): | 0.007 | 20% Bioavailability (F20%): | 0.004 |
30% Bioavailability (F30%): | 0.007 |
Blood-Brain-Barrier Penetration (BBB): | 0.965 | Plasma Protein Binding (PPB): | 63.14% |
Volume Distribution (VD): | 0.746 | Fu: | 20.23% |
CYP1A2-inhibitor: | 0.354 | CYP1A2-substrate: | 0.954 |
CYP2C19-inhibitor: | 0.07 | CYP2C19-substrate: | 0.903 |
CYP2C9-inhibitor: | 0.019 | CYP2C9-substrate: | 0.818 |
CYP2D6-inhibitor: | 0.031 | CYP2D6-substrate: | 0.723 |
CYP3A4-inhibitor: | 0.056 | CYP3A4-substrate: | 0.524 |
Clearance (CL): | 7.077 | Half-life (T1/2): | 0.5 |
hERG Blockers: | 0.008 | Human Hepatotoxicity (H-HT): | 0.193 |
Drug-inuced Liver Injury (DILI): | 0.323 | AMES Toxicity: | 0.067 |
Rat Oral Acute Toxicity: | 0.098 | Maximum Recommended Daily Dose: | 0.024 |
Skin Sensitization: | 0.055 | Carcinogencity: | 0.028 |
Eye Corrosion: | 0.003 | Eye Irritation: | 0.065 |
Respiratory Toxicity: | 0.065 |
Similar NPs | Similar Drugs | ||||||
---|---|---|---|---|---|---|---|
NPs ID | NPs 2D Structure | Similarity Score | TTD ID | Drug 2D Structure | Similarity Score | ||
ENC005163 | 0.750 | D0L1JW | 0.333 | ||||
ENC005556 | 0.745 | D04TDQ | 0.330 | ||||
ENC005907 | 0.684 | D0C1SF | 0.299 | ||||
ENC004991 | 0.525 | D0G4KG | 0.295 | ||||
ENC002669 | 0.517 | D0D4HN | 0.291 | ||||
ENC004498 | 0.453 | D09PJX | 0.287 | ||||
ENC004363 | 0.452 | D02LZB | 0.281 | ||||
ENC003612 | 0.434 | D06GCK | 0.272 | ||||
ENC000799 | 0.434 | D09DHY | 0.267 | ||||
ENC003801 | 0.434 | D0F7CS | 0.262 |