1-Deoxyviridiol

Details

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Internal ID 788725be-e03d-4669-9f58-f994656532cc
Taxonomy Benzenoids > Phenanthrenes and derivatives
IUPAC Name (1R,16R,17S)-16-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.02,10.05,9.015,19]nonadeca-2(10),3,5(9),12(19),14-pentaene-6,11-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H18O5/c1-20-7-14(24-2)17(22)11-8-25-19(16(11)20)18(23)15-10-4-6-13(21)9(10)3-5-12(15)20/h3,5,8,14,17,22H,4,6-7H2,1-2H3/t14-,17+,20+/m0/s1
InChI Key FRKJGFHTBOKCKM-JNAXZKDPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O5
Molecular Weight 338.40 g/mol
Exact Mass 338.11542367 g/mol
Topological Polar Surface Area (TPSA) 76.70 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.71
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Deoxyviridiol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9914 99.14%
Caco-2 + 0.6116 61.16%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7749 77.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8896 88.96%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6153 61.53%
P-glycoprotein inhibitior - 0.7147 71.47%
P-glycoprotein substrate - 0.5732 57.32%
CYP3A4 substrate + 0.7079 70.79%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.8060 80.60%
CYP3A4 inhibition - 0.7211 72.11%
CYP2C9 inhibition - 0.7736 77.36%
CYP2C19 inhibition - 0.8730 87.30%
CYP2D6 inhibition - 0.9053 90.53%
CYP1A2 inhibition - 0.5148 51.48%
CYP2C8 inhibition + 0.5745 57.45%
CYP inhibitory promiscuity - 0.8937 89.37%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5440 54.40%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9502 95.02%
Skin irritation - 0.7297 72.97%
Skin corrosion - 0.8809 88.09%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5885 58.85%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.8605 86.05%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6306 63.06%
Acute Oral Toxicity (c) III 0.5012 50.12%
Estrogen receptor binding + 0.6926 69.26%
Androgen receptor binding + 0.6500 65.00%
Thyroid receptor binding - 0.5724 57.24%
Glucocorticoid receptor binding + 0.7730 77.30%
Aromatase binding + 0.5905 59.05%
PPAR gamma + 0.7274 72.74%
Honey bee toxicity - 0.7270 72.70%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9482 94.82%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.77% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.25% 98.95%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 93.70% 96.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.02% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.74% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 91.72% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.07% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.28% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.63% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.49% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.41% 95.89%
CHEMBL1907 P15144 Aminopeptidase N 86.91% 93.31%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.40% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.43% 97.09%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.76% 96.67%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.29% 90.71%
CHEMBL259 P32245 Melanocortin receptor 4 80.13% 95.38%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 71573771
LOTUS LTS0251386
wikiData Q77279819