10-Hydroxythujopsene

Details

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Internal ID 05d44b06-fd3b-4f9e-906d-38cbe18ccc35
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1aR,4aR,7S,8aS)-2,4a,8,8-tetramethyl-1,1a,4,5,6,7-hexahydrocyclopropa[j]naphthalen-7-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10-5-7-14(4)8-6-12(16)13(2,3)15(14)9-11(10)15/h5,11-12,16H,6-9H2,1-4H3/t11-,12+,14+,15-/m1/s1
InChI Key RKYRGTWYGYBPFJ-PAPYEOQZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.53
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-Hydroxythujopsene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.7953 79.53%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.4641 46.41%
OATP2B1 inhibitior - 0.8441 84.41%
OATP1B1 inhibitior + 0.9280 92.80%
OATP1B3 inhibitior + 0.9428 94.28%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9082 90.82%
P-glycoprotein inhibitior - 0.9385 93.85%
P-glycoprotein substrate - 0.8748 87.48%
CYP3A4 substrate + 0.5428 54.28%
CYP2C9 substrate - 0.6107 61.07%
CYP2D6 substrate - 0.7019 70.19%
CYP3A4 inhibition - 0.7995 79.95%
CYP2C9 inhibition - 0.6385 63.85%
CYP2C19 inhibition - 0.6066 60.66%
CYP2D6 inhibition - 0.9362 93.62%
CYP1A2 inhibition - 0.7170 71.70%
CYP2C8 inhibition - 0.8750 87.50%
CYP inhibitory promiscuity - 0.7893 78.93%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5974 59.74%
Eye corrosion - 0.9854 98.54%
Eye irritation + 0.5479 54.79%
Skin irritation + 0.6249 62.49%
Skin corrosion - 0.9417 94.17%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5355 53.55%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.5551 55.51%
skin sensitisation + 0.6096 60.96%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.7251 72.51%
Acute Oral Toxicity (c) III 0.7913 79.13%
Estrogen receptor binding - 0.7809 78.09%
Androgen receptor binding - 0.5169 51.69%
Thyroid receptor binding - 0.6878 68.78%
Glucocorticoid receptor binding - 0.7280 72.80%
Aromatase binding - 0.6661 66.61%
PPAR gamma - 0.7386 73.86%
Honey bee toxicity - 0.9064 90.64%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9874 98.74%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.28% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.85% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 88.51% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.13% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.57% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.91% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.04% 95.89%
CHEMBL1871 P10275 Androgen Receptor 82.47% 96.43%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.13% 86.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.98% 92.94%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.40% 93.04%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.22% 95.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139585923
LOTUS LTS0147884
wikiData Q77494910