1-Methyl-5-methylidene-8-prop-1-en-2-ylcyclodeca-1,6-diene

Details

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Internal ID 4fbb015a-ccee-4b25-883a-fd18965ef9fc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 1-methyl-5-methylidene-8-prop-1-en-2-ylcyclodeca-1,6-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22/c1-12(2)15-10-8-13(3)6-5-7-14(4)9-11-15/h7-8,10,15H,1,3,5-6,9,11H2,2,4H3
InChI Key VPPSCJHEMMVYRU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.81
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 1-Methyl-5-methylidene-8-prop-1-en-2-ylcyclodeca-1,6-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 + 0.8491 84.91%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.6699 66.99%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9564 95.64%
OATP1B3 inhibitior + 0.9500 95.00%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7771 77.71%
P-glycoprotein inhibitior - 0.9547 95.47%
P-glycoprotein substrate - 0.8818 88.18%
CYP3A4 substrate - 0.5275 52.75%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7751 77.51%
CYP3A4 inhibition - 0.9326 93.26%
CYP2C9 inhibition - 0.8986 89.86%
CYP2C19 inhibition - 0.8577 85.77%
CYP2D6 inhibition - 0.9357 93.57%
CYP1A2 inhibition - 0.6595 65.95%
CYP2C8 inhibition - 0.7633 76.33%
CYP inhibitory promiscuity - 0.7749 77.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.4927 49.27%
Eye corrosion + 0.7142 71.42%
Eye irritation + 0.7116 71.16%
Skin irritation + 0.7176 71.76%
Skin corrosion - 0.9789 97.89%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4472 44.72%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.9314 93.14%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.5488 54.88%
Acute Oral Toxicity (c) III 0.8539 85.39%
Estrogen receptor binding - 0.9016 90.16%
Androgen receptor binding - 0.8433 84.33%
Thyroid receptor binding - 0.8130 81.30%
Glucocorticoid receptor binding - 0.6954 69.54%
Aromatase binding - 0.8643 86.43%
PPAR gamma - 0.6526 65.26%
Honey bee toxicity - 0.9000 90.00%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9967 99.67%

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 93.21% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.54% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.83% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.87% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 82.02% 91.49%
CHEMBL2581 P07339 Cathepsin D 81.75% 98.95%

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.
Psilostrophe villosa

Cross-Links

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PubChem 163069841
LOTUS LTS0087265
wikiData Q105290919