2-(4,8-Dimethylcyclodeca-2,7-dien-1-yl)propan-2-ol

Details

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Internal ID f2f2165b-428d-4e57-a7d8-2655dedb491b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 2-(4,8-dimethylcyclodeca-2,7-dien-1-yl)propan-2-ol
SMILES (Canonical) CC1CCC=C(CCC(C=C1)C(C)(C)O)C
SMILES (Isomeric) CC1CCC=C(CCC(C=C1)C(C)(C)O)C
InChI InChI=1S/C15H26O/c1-12-6-5-7-13(2)9-11-14(10-8-12)15(3,4)16/h6,9,11,13-14,16H,5,7-8,10H2,1-4H3
InChI Key ZVZPKUXZGROCDB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.09
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-(4,8-Dimethylcyclodeca-2,7-dien-1-yl)propan-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9929 99.29%
Caco-2 + 0.8429 84.29%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.4421 44.21%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9629 96.29%
OATP1B3 inhibitior + 0.9239 92.39%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.7360 73.60%
P-glycoprotein inhibitior - 0.9356 93.56%
P-glycoprotein substrate - 0.8745 87.45%
CYP3A4 substrate - 0.5664 56.64%
CYP2C9 substrate - 0.7759 77.59%
CYP2D6 substrate - 0.7764 77.64%
CYP3A4 inhibition - 0.8499 84.99%
CYP2C9 inhibition - 0.5563 55.63%
CYP2C19 inhibition - 0.6210 62.10%
CYP2D6 inhibition - 0.9308 93.08%
CYP1A2 inhibition - 0.7261 72.61%
CYP2C8 inhibition - 0.8011 80.11%
CYP inhibitory promiscuity - 0.7255 72.55%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7528 75.28%
Carcinogenicity (trinary) Non-required 0.5749 57.49%
Eye corrosion - 0.8491 84.91%
Eye irritation - 0.6559 65.59%
Skin irritation + 0.7414 74.14%
Skin corrosion - 0.9655 96.55%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5149 51.49%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5197 51.97%
skin sensitisation + 0.8579 85.79%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.7943 79.43%
Acute Oral Toxicity (c) IV 0.4987 49.87%
Estrogen receptor binding - 0.9255 92.55%
Androgen receptor binding - 0.8167 81.67%
Thyroid receptor binding - 0.5102 51.02%
Glucocorticoid receptor binding - 0.6143 61.43%
Aromatase binding - 0.8839 88.39%
PPAR gamma - 0.7953 79.53%
Honey bee toxicity - 0.9447 94.47%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9759 97.59%

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 98.05% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.68% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.99% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.05% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.73% 92.94%
CHEMBL1871 P10275 Androgen Receptor 83.00% 96.43%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 82.91% 90.93%
CHEMBL2581 P07339 Cathepsin D 82.50% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.90% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.74% 100.00%

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.
Dumortiera hirsuta
Ferula communis
Psidium guajava

Cross-Links

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PubChem 73237633
LOTUS LTS0229694
wikiData Q105384772