Longipinenone

Details

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Internal ID 33f1c368-0816-4049-8b28-09419bdd79bd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,2S)-2,6,6,11-tetramethyltricyclo[5.4.0.02,8]undec-10-en-9-one
SMILES (Canonical) CC1=CC(=O)C2C3C1C2(CCCC3(C)C)C
SMILES (Isomeric) CC1=CC(=O)C2C3[C@@H]1[C@@]2(CCCC3(C)C)C
InChI InChI=1S/C15H22O/c1-9-8-10(16)12-13-11(9)15(12,4)7-5-6-14(13,2)3/h8,11-13H,5-7H2,1-4H3/t11-,12?,13?,15+/m1/s1
InChI Key KTPOZFYJWLGJGH-LPXQKFACSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.59
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Longipinenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.8788 87.88%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.4596 45.96%
OATP2B1 inhibitior - 0.8473 84.73%
OATP1B1 inhibitior + 0.8662 86.62%
OATP1B3 inhibitior + 0.9476 94.76%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9513 95.13%
P-glycoprotein inhibitior - 0.8877 88.77%
P-glycoprotein substrate - 0.9420 94.20%
CYP3A4 substrate + 0.5286 52.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8716 87.16%
CYP3A4 inhibition - 0.8587 85.87%
CYP2C9 inhibition - 0.7124 71.24%
CYP2C19 inhibition - 0.5273 52.73%
CYP2D6 inhibition - 0.8748 87.48%
CYP1A2 inhibition - 0.6658 66.58%
CYP2C8 inhibition - 0.9284 92.84%
CYP inhibitory promiscuity - 0.7016 70.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.4382 43.82%
Eye corrosion - 0.9667 96.67%
Eye irritation - 0.5683 56.83%
Skin irritation + 0.6182 61.82%
Skin corrosion - 0.9321 93.21%
Ames mutagenesis - 0.8123 81.23%
Human Ether-a-go-go-Related Gene inhibition - 0.5289 52.89%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5699 56.99%
skin sensitisation + 0.7849 78.49%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6040 60.40%
Acute Oral Toxicity (c) III 0.7735 77.35%
Estrogen receptor binding - 0.5453 54.53%
Androgen receptor binding + 0.5497 54.97%
Thyroid receptor binding - 0.5438 54.38%
Glucocorticoid receptor binding - 0.7464 74.64%
Aromatase binding - 0.7648 76.48%
PPAR gamma - 0.7170 71.70%
Honey bee toxicity - 0.9145 91.45%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9654 96.54%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.18% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.37% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.27% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 87.23% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.90% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.86% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.56% 93.99%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.24% 93.04%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.91% 86.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.37% 96.09%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 82.60% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.53% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.15% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.52% 99.23%

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.
Schisandra chinensis
Schisandra sphenanthera

Cross-Links

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PubChem 101117096
NPASS NPC153195