(-)-8beta-Presilphiperfolanol

Details

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Internal ID 172ca86a-8165-4460-8cc1-da9b2deb4bb9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,4R,7R,8S,11S)-2,2,4,8-tetramethyltricyclo[5.3.1.04,11]undecan-11-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O/c1-10-5-6-12-13(2,3)9-14(4)8-7-11(10)15(12,14)16/h10-12,16H,5-9H2,1-4H3/t10-,11+,12+,14+,15-/m0/s1
InChI Key ZCRYDCBITZERMT-PRSHDEELSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.61
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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LMPR0103750002

2D Structure

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2D Structure of (-)-8beta-Presilphiperfolanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.7254 72.54%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.5269 52.69%
OATP2B1 inhibitior - 0.8441 84.41%
OATP1B1 inhibitior + 0.9109 91.09%
OATP1B3 inhibitior + 0.9316 93.16%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8668 86.68%
P-glycoprotein inhibitior - 0.9319 93.19%
P-glycoprotein substrate - 0.8966 89.66%
CYP3A4 substrate + 0.5863 58.63%
CYP2C9 substrate + 0.6248 62.48%
CYP2D6 substrate - 0.7422 74.22%
CYP3A4 inhibition - 0.8892 88.92%
CYP2C9 inhibition - 0.7398 73.98%
CYP2C19 inhibition - 0.8778 87.78%
CYP2D6 inhibition - 0.9640 96.40%
CYP1A2 inhibition - 0.5679 56.79%
CYP2C8 inhibition - 0.7290 72.90%
CYP inhibitory promiscuity - 0.9015 90.15%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6441 64.41%
Eye corrosion - 0.8859 88.59%
Eye irritation + 0.8627 86.27%
Skin irritation + 0.7217 72.17%
Skin corrosion - 0.8705 87.05%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5075 50.75%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5457 54.57%
skin sensitisation + 0.7169 71.69%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7681 76.81%
Acute Oral Toxicity (c) III 0.7793 77.93%
Estrogen receptor binding - 0.5706 57.06%
Androgen receptor binding + 0.6106 61.06%
Thyroid receptor binding - 0.6376 63.76%
Glucocorticoid receptor binding - 0.7753 77.53%
Aromatase binding - 0.6148 61.48%
PPAR gamma - 0.6950 69.50%
Honey bee toxicity - 0.9033 90.33%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9740 97.40%

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 97.22% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.07% 96.09%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 87.60% 91.03%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.38% 91.11%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.38% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.17% 97.09%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 82.55% 98.99%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.52% 96.38%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.51% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.03% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.30% 95.89%

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.
Callilepis salicifolia

Cross-Links

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PubChem 42608190
LOTUS LTS0212204
wikiData Q105371405