1,5-Dimethyl-8-(6-methylhepta-1,5-dien-2-yl)cyclodeca-1,5-diene

Details

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Internal ID 8bd7c8b6-56d2-49e3-8818-e48edb1756f4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 1,5-dimethyl-8-(6-methylhepta-1,5-dien-2-yl)cyclodeca-1,5-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32/c1-16(2)8-6-11-19(5)20-14-12-17(3)9-7-10-18(4)13-15-20/h8-9,13,20H,5-7,10-12,14-15H2,1-4H3
InChI Key QJPIQRLACCGVNH-UHFFFAOYSA-N
Popularity 0 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) 6.76
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,5-Dimethyl-8-(6-methylhepta-1,5-dien-2-yl)cyclodeca-1,5-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9914 99.14%
Caco-2 + 0.9004 90.04%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Nucleus 0.4309 43.09%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.9405 94.05%
OATP1B3 inhibitior + 0.9418 94.18%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.6523 65.23%
P-glycoprotein substrate - 0.8881 88.81%
CYP3A4 substrate - 0.5108 51.08%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9304 93.04%
CYP2C9 inhibition - 0.8300 83.00%
CYP2C19 inhibition - 0.8191 81.91%
CYP2D6 inhibition - 0.9397 93.97%
CYP1A2 inhibition - 0.6458 64.58%
CYP2C8 inhibition - 0.7186 71.86%
CYP inhibitory promiscuity - 0.6717 67.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Warning 0.4872 48.72%
Eye corrosion + 0.4905 49.05%
Eye irritation - 0.5589 55.89%
Skin irritation + 0.7172 71.72%
Skin corrosion - 0.9709 97.09%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8066 80.66%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.9204 92.04%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.6144 61.44%
Acute Oral Toxicity (c) III 0.8757 87.57%
Estrogen receptor binding - 0.7875 78.75%
Androgen receptor binding - 0.7129 71.29%
Thyroid receptor binding - 0.5609 56.09%
Glucocorticoid receptor binding - 0.5298 52.98%
Aromatase binding - 0.7498 74.98%
PPAR gamma + 0.7105 71.05%
Honey bee toxicity - 0.8945 89.45%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9974 99.74%

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 97.18% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.26% 97.25%
CHEMBL2581 P07339 Cathepsin D 88.74% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.76% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.08% 96.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.76% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.48% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 81.42% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.64% 95.56%

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.
Helichrysum argyrophyllum

Cross-Links

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PubChem 163042798
LOTUS LTS0235349
wikiData Q105222802