beta-Duprezianane

Details

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Internal ID 037f7378-5923-416a-aa6c-9bdff54350e9
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (1R,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.2.2.01,5]undecane
SMILES (Canonical) CC1CCC2C13CCC(C2(C)C)C(=C)C3
SMILES (Isomeric) C[C@@H]1CC[C@@H]2[C@@]13CC[C@H](C2(C)C)C(=C)C3
InChI InChI=1S/C15H24/c1-10-9-15-8-7-12(10)14(3,4)13(15)6-5-11(15)2/h11-13H,1,5-9H2,2-4H3/t11-,12+,13+,15-/m1/s1
InChI Key SODGFMASLAAZRW-UKTARXLSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.42
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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.beta.-Duprezianene
SODGFMASLAAZRW-UKTARXLSSA-N

2D Structure

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2D Structure of beta-Duprezianane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.7110 71.10%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.7057 70.57%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.9113 91.13%
OATP1B3 inhibitior + 0.8561 85.61%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9069 90.69%
P-glycoprotein inhibitior - 0.9104 91.04%
P-glycoprotein substrate - 0.8897 88.97%
CYP3A4 substrate + 0.5303 53.03%
CYP2C9 substrate - 0.6027 60.27%
CYP2D6 substrate - 0.7518 75.18%
CYP3A4 inhibition - 0.8252 82.52%
CYP2C9 inhibition - 0.6901 69.01%
CYP2C19 inhibition - 0.5470 54.70%
CYP2D6 inhibition - 0.9255 92.55%
CYP1A2 inhibition - 0.8204 82.04%
CYP2C8 inhibition - 0.8977 89.77%
CYP inhibitory promiscuity - 0.5776 57.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.4615 46.15%
Eye corrosion - 0.9384 93.84%
Eye irritation + 0.8635 86.35%
Skin irritation - 0.6318 63.18%
Skin corrosion - 0.9695 96.95%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4554 45.54%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5459 54.59%
skin sensitisation + 0.8329 83.29%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.5696 56.96%
Acute Oral Toxicity (c) III 0.8080 80.80%
Estrogen receptor binding - 0.7889 78.89%
Androgen receptor binding + 0.5326 53.26%
Thyroid receptor binding - 0.7388 73.88%
Glucocorticoid receptor binding - 0.7794 77.94%
Aromatase binding - 0.8112 81.12%
PPAR gamma - 0.7988 79.88%
Honey bee toxicity - 0.8374 83.74%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.77% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 89.62% 90.17%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.06% 82.69%
CHEMBL1951 P21397 Monoamine oxidase A 85.22% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.21% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.17% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.92% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.60% 96.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.70% 86.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.86% 92.94%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 81.37% 95.27%
CHEMBL233 P35372 Mu opioid receptor 80.34% 97.93%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.19% 91.03%

Cross-Links

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PubChem 91750164
NPASS NPC32938
LOTUS LTS0228607
wikiData Q105256863