Pimara-8,15-diene

Details

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Internal ID cb929f6a-6852-43d6-a149-5fa75bd87679
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (2R,4bS,8aS)-2-ethenyl-2,4b,8,8-tetramethyl-3,4,5,6,7,8a,9,10-octahydro-1H-phenanthrene
SMILES (Canonical) CC1(CCCC2(C1CCC3=C2CCC(C3)(C)C=C)C)C
SMILES (Isomeric) C[C@]1(CCC2=C(C1)CC[C@@H]3[C@@]2(CCCC3(C)C)C)C=C
InChI InChI=1S/C20H32/c1-6-19(4)13-10-16-15(14-19)8-9-17-18(2,3)11-7-12-20(16,17)5/h6,17H,1,7-14H2,2-5H3/t17-,19+,20+/m0/s1
InChI Key OROJBMPJDLLRFD-DFQSSKMNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32
Molecular Weight 272.50 g/mol
Exact Mass 272.250401021 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.50
Atomic LogP (AlogP) 6.29
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pimara-8,15-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.8815 88.15%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.6716 67.16%
OATP2B1 inhibitior - 0.8525 85.25%
OATP1B1 inhibitior + 0.8915 89.15%
OATP1B3 inhibitior + 0.8873 88.73%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.6381 63.81%
P-glycoprotein inhibitior - 0.7982 79.82%
P-glycoprotein substrate - 0.9268 92.68%
CYP3A4 substrate + 0.5802 58.02%
CYP2C9 substrate - 0.7731 77.31%
CYP2D6 substrate - 0.7252 72.52%
CYP3A4 inhibition - 0.8545 85.45%
CYP2C9 inhibition - 0.5747 57.47%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.9203 92.03%
CYP1A2 inhibition - 0.8124 81.24%
CYP2C8 inhibition - 0.5794 57.94%
CYP inhibitory promiscuity - 0.6444 64.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4673 46.73%
Eye corrosion - 0.9327 93.27%
Eye irritation - 0.5741 57.41%
Skin irritation - 0.6695 66.95%
Skin corrosion - 0.9642 96.42%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7451 74.51%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5031 50.31%
skin sensitisation + 0.8009 80.09%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5474 54.74%
Acute Oral Toxicity (c) III 0.8150 81.50%
Estrogen receptor binding - 0.6148 61.48%
Androgen receptor binding + 0.5943 59.43%
Thyroid receptor binding - 0.5399 53.99%
Glucocorticoid receptor binding + 0.5470 54.70%
Aromatase binding - 0.6449 64.49%
PPAR gamma - 0.5904 59.04%
Honey bee toxicity - 0.8133 81.33%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.41% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.12% 97.25%
CHEMBL1902 P62942 FK506-binding protein 1A 88.74% 97.05%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.43% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.95% 97.09%
CHEMBL1951 P21397 Monoamine oxidase A 86.12% 91.49%
CHEMBL1871 P10275 Androgen Receptor 83.93% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.15% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.39% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.34% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.92% 95.56%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.11% 95.50%

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.
Cistus creticus
Prumnopitys andina

Cross-Links

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PubChem 13783134
LOTUS LTS0229334
wikiData Q77496294