Npc77989

Details

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Internal ID d55bb24d-a3c0-4b49-b358-4e88c165c6df
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2,2,4,8-tetramethyltricyclo[5.3.1.04,11]undec-8-ene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24/c1-10-5-6-12-13-11(10)7-8-15(13,4)9-14(12,2)3/h5,11-13H,6-9H2,1-4H3
InChI Key SXDGNLAJFYRAOG-UHFFFAOYSA-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 4.60
Atomic LogP (AlogP) 4.42
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Npc77989
SCHEMBL16820309
SXDGNLAJFYRAOG-UHFFFAOYSA-N
1R,4S,7S,11R-2,2,4,8-Tetramethyltricyclo[5.3.1.0(4,11)]undec-8-ene
2a,4,4,7-Tetramethyl-2,2a,3,4,4a,5,7a,7b-octahydro-1H-cyclopenta[cd]indene #

2D Structure

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2D Structure of Npc77989

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.8478 84.78%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.7261 72.61%
OATP2B1 inhibitior - 0.8442 84.42%
OATP1B1 inhibitior + 0.9294 92.94%
OATP1B3 inhibitior + 0.9397 93.97%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9054 90.54%
P-glycoprotein inhibitior - 0.9397 93.97%
P-glycoprotein substrate - 0.9067 90.67%
CYP3A4 substrate + 0.5491 54.91%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.8715 87.15%
CYP2C9 inhibition - 0.7890 78.90%
CYP2C19 inhibition - 0.7343 73.43%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.8212 82.12%
CYP2C8 inhibition - 0.6569 65.69%
CYP inhibitory promiscuity - 0.6962 69.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Warning 0.4809 48.09%
Eye corrosion - 0.9117 91.17%
Eye irritation + 0.7743 77.43%
Skin irritation + 0.6056 60.56%
Skin corrosion - 0.9765 97.65%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6415 64.15%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5774 57.74%
skin sensitisation + 0.9014 90.14%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.5914 59.14%
Acute Oral Toxicity (c) III 0.6284 62.84%
Estrogen receptor binding - 0.8523 85.23%
Androgen receptor binding + 0.6131 61.31%
Thyroid receptor binding - 0.7613 76.13%
Glucocorticoid receptor binding - 0.8656 86.56%
Aromatase binding - 0.8513 85.13%
PPAR gamma - 0.7968 79.68%
Honey bee toxicity - 0.8551 85.51%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.9971 99.71%

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 92.75% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.02% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.35% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.35% 100.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.03% 86.00%
CHEMBL1871 P10275 Androgen Receptor 82.21% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.10% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 81.48% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.02% 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.
Hansenia forbesii
Hansenia weberbaueriana

Cross-Links

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PubChem 573293
NPASS NPC77989