4,14,15,15-Tetramethyl-8-methylidenebicyclo[9.3.1]pentadeca-1(14),4-diene

Details

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Internal ID c0f241cb-6f7a-4b65-ae9f-61f9436e7302
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 4,14,15,15-tetramethyl-8-methylidenebicyclo[9.3.1]pentadeca-1(14),4-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32/c1-15-7-6-8-16(2)10-14-19-17(3)11-13-18(12-9-15)20(19,4)5/h8,18H,1,6-7,9-14H2,2-5H3
InChI Key SNPPNYAGNBWZCL-UHFFFAOYSA-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 5.40
Atomic LogP (AlogP) 6.60
H-Bond Acceptor 0
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 4,14,15,15-Tetramethyl-8-methylidenebicyclo[9.3.1]pentadeca-1(14),4-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 + 0.9217 92.17%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.7300 73.00%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9281 92.81%
OATP1B3 inhibitior + 0.9190 91.90%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.6145 61.45%
P-glycoprotein inhibitior - 0.7713 77.13%
P-glycoprotein substrate - 0.8798 87.98%
CYP3A4 substrate + 0.5397 53.97%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.7846 78.46%
CYP3A4 inhibition - 0.8732 87.32%
CYP2C9 inhibition - 0.6397 63.97%
CYP2C19 inhibition - 0.6243 62.43%
CYP2D6 inhibition - 0.9285 92.85%
CYP1A2 inhibition - 0.7735 77.35%
CYP2C8 inhibition - 0.7406 74.06%
CYP inhibitory promiscuity - 0.7789 77.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Warning 0.4950 49.50%
Eye corrosion - 0.8833 88.33%
Eye irritation + 0.5739 57.39%
Skin irritation + 0.5331 53.31%
Skin corrosion - 0.9773 97.73%
Ames mutagenesis - 0.8215 82.15%
Human Ether-a-go-go-Related Gene inhibition + 0.8202 82.02%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.8484 84.84%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.5542 55.42%
Acute Oral Toxicity (c) III 0.7832 78.32%
Estrogen receptor binding - 0.7009 70.09%
Androgen receptor binding - 0.5981 59.81%
Thyroid receptor binding - 0.6044 60.44%
Glucocorticoid receptor binding - 0.4816 48.16%
Aromatase binding - 0.5319 53.19%
PPAR gamma - 0.5998 59.98%
Honey bee toxicity - 0.9113 91.13%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6600 66.00%
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 91.38% 97.25%
CHEMBL1871 P10275 Androgen Receptor 90.72% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.90% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.85% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.40% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.50% 100.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.58% 86.00%
CHEMBL2581 P07339 Cathepsin D 83.57% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.13% 97.09%

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.
Bursera kerberi

Cross-Links

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PubChem 73200960
LOTUS LTS0151312
wikiData Q103815935