Presilphiperfol-7-ene

Details

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Internal ID e8482e62-c1ae-498b-afab-381ddc34a321
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4S,8R)-2,2,4,8-tetramethyltricyclo[5.3.1.04,11]undec-1(11)-ene
SMILES (Canonical) CC1CCC2=C3C1CCC3(CC2(C)C)C
SMILES (Isomeric) C[C@@H]1CCC2=C3C1CC[C@]3(CC2(C)C)C
InChI InChI=1S/C15H24/c1-10-5-6-12-13-11(10)7-8-15(13,4)9-14(12,2)3/h10-11H,5-9H2,1-4H3/t10-,11?,15+/m1/s1
InChI Key PLHQUFSAXMJRAY-JRDMHLJOSA-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 4.50
Atomic LogP (AlogP) 4.56
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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PLHQUFSAXMJRAY-JRDMHLJOSA-N
Q67880062

2D Structure

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2D Structure of Presilphiperfol-7-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.8212 82.12%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.7186 71.86%
OATP2B1 inhibitior - 0.8413 84.13%
OATP1B1 inhibitior + 0.8857 88.57%
OATP1B3 inhibitior + 0.9521 95.21%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8444 84.44%
P-glycoprotein inhibitior - 0.9246 92.46%
P-glycoprotein substrate - 0.9060 90.60%
CYP3A4 substrate + 0.5133 51.33%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.9005 90.05%
CYP2C9 inhibition - 0.7302 73.02%
CYP2C19 inhibition - 0.6980 69.80%
CYP2D6 inhibition - 0.9335 93.35%
CYP1A2 inhibition - 0.8114 81.14%
CYP2C8 inhibition - 0.7571 75.71%
CYP inhibitory promiscuity - 0.6924 69.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Warning 0.4740 47.40%
Eye corrosion - 0.9232 92.32%
Eye irritation + 0.9050 90.50%
Skin irritation + 0.5325 53.25%
Skin corrosion - 0.9756 97.56%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4284 42.84%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6228 62.28%
skin sensitisation + 0.8722 87.22%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6404 64.04%
Acute Oral Toxicity (c) III 0.6583 65.83%
Estrogen receptor binding - 0.8886 88.86%
Androgen receptor binding + 0.6748 67.48%
Thyroid receptor binding - 0.7099 70.99%
Glucocorticoid receptor binding - 0.8524 85.24%
Aromatase binding - 0.7655 76.55%
PPAR gamma - 0.8670 86.70%
Honey bee toxicity - 0.8663 86.63%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity + 0.9974 99.74%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.34% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.76% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.18% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.70% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.74% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.25% 95.56%

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.
Echinops giganteus

Cross-Links

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PubChem 91746704
LOTUS LTS0011248
wikiData Q67880062