(1Z,5Z,7S)-1,5-dimethyl-7-prop-1-en-2-ylcyclodeca-1,5-diene

Details

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Internal ID 526cdc43-4652-4f21-a8c8-fa43205d9205
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (1Z,5Z,7S)-1,5-dimethyl-7-prop-1-en-2-ylcyclodeca-1,5-diene
SMILES (Canonical) CC1=CCCC(=CC(CCC1)C(=C)C)C
SMILES (Isomeric) C/C/1=C/CC/C(=C\[C@H](CCC1)C(=C)C)/C
InChI InChI=1S/C15H24/c1-12(2)15-10-6-8-13(3)7-5-9-14(4)11-15/h7,11,15H,1,5-6,8-10H2,2-4H3/b13-7-,14-11-/t15-/m0/s1
InChI Key YSOYXLPARMWZFY-CXWCYCAGSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 5.04
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 (1Z,5Z,7S)-1,5-dimethyl-7-prop-1-en-2-ylcyclodeca-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 + 0.9915 99.15%
Caco-2 + 0.9722 97.22%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.5878 58.78%
OATP2B1 inhibitior - 0.8495 84.95%
OATP1B1 inhibitior + 0.9588 95.88%
OATP1B3 inhibitior + 0.9473 94.73%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.5877 58.77%
P-glycoprotein inhibitior - 0.9270 92.70%
P-glycoprotein substrate - 0.8961 89.61%
CYP3A4 substrate - 0.5807 58.07%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9207 92.07%
CYP2C9 inhibition - 0.8613 86.13%
CYP2C19 inhibition - 0.8203 82.03%
CYP2D6 inhibition - 0.9379 93.79%
CYP1A2 inhibition - 0.6699 66.99%
CYP2C8 inhibition - 0.8378 83.78%
CYP inhibitory promiscuity - 0.7682 76.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Warning 0.4978 49.78%
Eye corrosion + 0.5909 59.09%
Eye irritation + 0.7587 75.87%
Skin irritation + 0.7468 74.68%
Skin corrosion - 0.9749 97.49%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6471 64.71%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6282 62.82%
skin sensitisation + 0.8923 89.23%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.5617 56.17%
Acute Oral Toxicity (c) III 0.8499 84.99%
Estrogen receptor binding - 0.9677 96.77%
Androgen receptor binding - 0.9006 90.06%
Thyroid receptor binding - 0.7534 75.34%
Glucocorticoid receptor binding - 0.8064 80.64%
Aromatase binding - 0.8260 82.60%
PPAR gamma - 0.8163 81.63%
Honey bee toxicity - 0.9303 93.03%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9965 99.65%

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 95.30% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 90.70% 91.49%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.90% 97.25%
CHEMBL2581 P07339 Cathepsin D 88.60% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.62% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.75% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.04% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.13% 92.94%

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.
Saccogyna viticulosa

Cross-Links

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PubChem 101349813
LOTUS LTS0088891
wikiData Q105360378