Caparratriene

Details

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Internal ID a8c6f141-1915-42ee-9d02-6721b4982526
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E,4E,7R)-3,7,11-trimethyldodeca-2,4,10-triene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26/c1-6-14(4)10-8-12-15(5)11-7-9-13(2)3/h6,8-10,15H,7,11-12H2,1-5H3/b10-8+,14-6+/t15-/m1/s1
InChI Key GIBJEWOSWWYJSK-WNMJCELSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26
Molecular Weight 206.37 g/mol
Exact Mass 206.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.10
Atomic LogP (AlogP) 5.28
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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CHEMBL499267
2,4,10-Dodecatriene, 3,7,11-trimethyl-,(2E,4E,7R)-

2D Structure

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2D Structure of Caparratriene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9871 98.71%
Caco-2 + 0.9788 97.88%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Nucleus 0.7729 77.29%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.9164 91.64%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7626 76.26%
P-glycoprotein inhibitior - 0.9809 98.09%
P-glycoprotein substrate - 0.9037 90.37%
CYP3A4 substrate - 0.5930 59.30%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7751 77.51%
CYP3A4 inhibition - 0.9631 96.31%
CYP2C9 inhibition - 0.9136 91.36%
CYP2C19 inhibition - 0.9113 91.13%
CYP2D6 inhibition - 0.9389 93.89%
CYP1A2 inhibition - 0.7285 72.85%
CYP2C8 inhibition - 0.9837 98.37%
CYP inhibitory promiscuity - 0.6642 66.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Warning 0.4833 48.33%
Eye corrosion + 0.6599 65.99%
Eye irritation + 0.7695 76.95%
Skin irritation + 0.9090 90.90%
Skin corrosion - 0.9348 93.48%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6531 65.31%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5225 52.25%
skin sensitisation + 0.9482 94.82%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.4724 47.24%
Acute Oral Toxicity (c) III 0.8841 88.41%
Estrogen receptor binding - 0.9360 93.60%
Androgen receptor binding - 0.8976 89.76%
Thyroid receptor binding - 0.6616 66.16%
Glucocorticoid receptor binding - 0.7717 77.17%
Aromatase binding - 0.8904 89.04%
PPAR gamma - 0.8572 85.72%
Honey bee toxicity - 0.9293 92.93%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9808 98.08%

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
CHEMBL221 P23219 Cyclooxygenase-1 91.25% 90.17%
CHEMBL2581 P07339 Cathepsin D 87.33% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.61% 94.45%
CHEMBL2885 P07451 Carbonic anhydrase III 85.06% 87.45%
CHEMBL3401 O75469 Pregnane X receptor 82.58% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.00% 89.34%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 6442208
LOTUS LTS0235121
wikiData Q105008853