3beta-Hydroxycedrene

Details

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Internal ID ff9521be-e5b4-4f2c-bc31-86589d9fa9c3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Cedrane and isocedrane sesquiterpenoids
IUPAC Name (1R,2S,3R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-en-3-ol
SMILES (Canonical) CC1C(CC2C13CC=C(C(C3)C2(C)C)C)O
SMILES (Isomeric) C[C@@H]1[C@@H](C[C@@H]2[C@]13CC=C([C@H](C3)C2(C)C)C)O
InChI InChI=1S/C15H24O/c1-9-5-6-15-8-11(9)14(3,4)13(15)7-12(16)10(15)2/h5,10-13,16H,6-8H2,1-4H3/t10-,11+,12-,13+,15+/m1/s1
InChI Key CLLPJTJAWPETTB-JYKNGBAOSA-N
Popularity 0 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 3.30
Atomic LogP (AlogP) 3.39
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 3beta-Hydroxycedrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.6329 63.29%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.6418 64.18%
OATP2B1 inhibitior - 0.8496 84.96%
OATP1B1 inhibitior + 0.9300 93.00%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9090 90.90%
P-glycoprotein inhibitior - 0.9572 95.72%
P-glycoprotein substrate - 0.7506 75.06%
CYP3A4 substrate + 0.5408 54.08%
CYP2C9 substrate - 0.6077 60.77%
CYP2D6 substrate - 0.7196 71.96%
CYP3A4 inhibition - 0.8535 85.35%
CYP2C9 inhibition - 0.8277 82.77%
CYP2C19 inhibition - 0.7388 73.88%
CYP2D6 inhibition - 0.9433 94.33%
CYP1A2 inhibition - 0.7900 79.00%
CYP2C8 inhibition - 0.9296 92.96%
CYP inhibitory promiscuity - 0.7843 78.43%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8124 81.24%
Carcinogenicity (trinary) Non-required 0.5876 58.76%
Eye corrosion - 0.9715 97.15%
Eye irritation - 0.7402 74.02%
Skin irritation + 0.7174 71.74%
Skin corrosion - 0.9175 91.75%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4347 43.47%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.6155 61.55%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.8389 83.89%
Acute Oral Toxicity (c) III 0.7113 71.13%
Estrogen receptor binding - 0.8779 87.79%
Androgen receptor binding - 0.6507 65.07%
Thyroid receptor binding - 0.7428 74.28%
Glucocorticoid receptor binding - 0.7508 75.08%
Aromatase binding - 0.8077 80.77%
PPAR gamma - 0.7109 71.09%
Honey bee toxicity - 0.8434 84.34%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9639 96.39%

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 93.85% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.68% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.95% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.48% 97.09%
CHEMBL1951 P21397 Monoamine oxidase A 88.31% 91.49%
CHEMBL221 P23219 Cyclooxygenase-1 86.24% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.21% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.40% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.71% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.61% 86.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.51% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.49% 96.95%

Cross-Links

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PubChem 15215015
NPASS NPC188650
LOTUS LTS0009066
wikiData Q104963599