2-Methyl-8-methylidene-5-propan-2-ylcyclodeca-2,6-dien-1-ol

Details

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Internal ID 5d91ec6c-c280-4359-8dfe-fc046a09a610
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 2-methyl-8-methylidene-5-propan-2-ylcyclodeca-2,6-dien-1-ol
SMILES (Canonical) CC1=CCC(C=CC(=C)CCC1O)C(C)C
SMILES (Isomeric) CC1=CCC(C=CC(=C)CCC1O)C(C)C
InChI InChI=1S/C15H24O/c1-11(2)14-8-5-12(3)6-10-15(16)13(4)7-9-14/h5,7-8,11,14-16H,3,6,9-10H2,1-2,4H3
InChI Key KMNKEJZZENNJLR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.86
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Methyl-8-methylidene-5-propan-2-ylcyclodeca-2,6-dien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.8324 83.24%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.4353 43.53%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.9427 94.27%
OATP1B3 inhibitior + 0.9085 90.85%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8222 82.22%
P-glycoprotein inhibitior - 0.9440 94.40%
P-glycoprotein substrate - 0.8572 85.72%
CYP3A4 substrate - 0.5674 56.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7555 75.55%
CYP3A4 inhibition - 0.9256 92.56%
CYP2C9 inhibition - 0.8509 85.09%
CYP2C19 inhibition - 0.8070 80.70%
CYP2D6 inhibition - 0.9144 91.44%
CYP1A2 inhibition - 0.7643 76.43%
CYP2C8 inhibition - 0.9034 90.34%
CYP inhibitory promiscuity - 0.8510 85.10%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Non-required 0.6760 67.60%
Eye corrosion - 0.8762 87.62%
Eye irritation - 0.6202 62.02%
Skin irritation + 0.6833 68.33%
Skin corrosion - 0.8688 86.88%
Ames mutagenesis - 0.7964 79.64%
Human Ether-a-go-go-Related Gene inhibition - 0.4242 42.42%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.7277 72.77%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5164 51.64%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.8809 88.09%
Acute Oral Toxicity (c) III 0.7325 73.25%
Estrogen receptor binding - 0.8857 88.57%
Androgen receptor binding - 0.8532 85.32%
Thyroid receptor binding - 0.6187 61.87%
Glucocorticoid receptor binding - 0.4673 46.73%
Aromatase binding - 0.8526 85.26%
PPAR gamma - 0.7037 70.37%
Honey bee toxicity - 0.8675 86.75%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.8873 88.73%

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
CHEMBL3359 P21462 Formyl peptide receptor 1 89.88% 93.56%
CHEMBL2581 P07339 Cathepsin D 87.22% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.81% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.03% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.21% 95.89%
CHEMBL1977 P11473 Vitamin D receptor 82.98% 99.43%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.91% 96.47%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.80% 90.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.34% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.25% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.96% 96.09%
CHEMBL1871 P10275 Androgen Receptor 81.20% 96.43%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.21% 97.25%

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.
Senecio philippicus

Cross-Links

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PubChem 163032052
LOTUS LTS0257422
wikiData Q105143053