Syn-pimaradiene

Details

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Internal ID 3c76514f-8700-42cf-adae-6178bc4b8757
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (2R,4aS,4bS,8aS)-2-ethenyl-2,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthrene
SMILES (Canonical) CC1(CCCC2(C1CC=C3C2CCC(C3)(C)C=C)C)C
SMILES (Isomeric) C[C@]1(CC[C@H]2C(=CC[C@@H]3[C@@]2(CCCC3(C)C)C)C1)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/h6,8,16-17H,1,7,9-14H2,2-5H3/t16-,17-,19+,20+/m0/s1
InChI Key VCOVNILQQQZROK-RAUXBKROSA-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 6.80
Atomic LogP (AlogP) 6.14
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 Syn-pimaradiene

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 + 0.8457 84.57%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.6716 67.16%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.8863 88.63%
OATP1B3 inhibitior + 0.8873 88.73%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.8387 83.87%
P-glycoprotein substrate - 0.9000 90.00%
CYP3A4 substrate + 0.5636 56.36%
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 - 0.6161 61.61%
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 - 0.8559 85.59%
Skin irritation - 0.6695 66.95%
Skin corrosion - 0.9642 96.42%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8190 81.90%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5459 54.59%
skin sensitisation + 0.8009 80.09%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8150 81.50%
Estrogen receptor binding - 0.5309 53.09%
Androgen receptor binding + 0.5545 55.45%
Thyroid receptor binding - 0.4920 49.20%
Glucocorticoid receptor binding + 0.6141 61.41%
Aromatase binding - 0.6421 64.21%
PPAR gamma - 0.5598 55.98%
Honey bee toxicity - 0.8217 82.17%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6900 69.00%
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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.75% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.66% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 90.77% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.18% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.31% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.55% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.07% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 84.72% 90.17%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 83.95% 91.03%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.30% 82.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.01% 94.45%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.15% 99.18%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 80.82% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.74% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.72% 92.94%
CHEMBL2664 P23526 Adenosylhomocysteinase 80.39% 86.67%

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.
Pinus densiflora

Cross-Links

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PubChem 21126013
LOTUS LTS0182469
wikiData Q105283862