1,5-Dimethyl-7-(2-methylprop-1-enyl)cyclonon-4-en-1-ol

Details

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Internal ID 5b6c6598-850b-4b73-bb97-d83594c18e59
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 1,5-dimethyl-7-(2-methylprop-1-enyl)cyclonon-4-en-1-ol
SMILES (Canonical) CC1=CCCC(CCC(C1)C=C(C)C)(C)O
SMILES (Isomeric) CC1=CCCC(CCC(C1)C=C(C)C)(C)O
InChI InChI=1S/C15H26O/c1-12(2)10-14-7-9-15(4,16)8-5-6-13(3)11-14/h6,10,14,16H,5,7-9,11H2,1-4H3
InChI Key FKVGWGFRHBPOHC-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 3.70
Atomic LogP (AlogP) 4.23
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 1,5-Dimethyl-7-(2-methylprop-1-enyl)cyclonon-4-en-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 + 0.9968 99.68%
Caco-2 + 0.9154 91.54%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.4231 42.31%
OATP2B1 inhibitior - 0.8471 84.71%
OATP1B1 inhibitior + 0.9516 95.16%
OATP1B3 inhibitior + 0.9624 96.24%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8388 83.88%
P-glycoprotein inhibitior - 0.9687 96.87%
P-glycoprotein substrate - 0.8902 89.02%
CYP3A4 substrate - 0.5115 51.15%
CYP2C9 substrate - 0.5790 57.90%
CYP2D6 substrate - 0.7630 76.30%
CYP3A4 inhibition - 0.8491 84.91%
CYP2C9 inhibition - 0.8021 80.21%
CYP2C19 inhibition - 0.8452 84.52%
CYP2D6 inhibition - 0.9424 94.24%
CYP1A2 inhibition - 0.7819 78.19%
CYP2C8 inhibition - 0.8004 80.04%
CYP inhibitory promiscuity - 0.9170 91.70%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.5904 59.04%
Eye corrosion - 0.9038 90.38%
Eye irritation + 0.5824 58.24%
Skin irritation + 0.7754 77.54%
Skin corrosion - 0.9561 95.61%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4598 45.98%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5101 51.01%
skin sensitisation + 0.8315 83.15%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.5162 51.62%
Acute Oral Toxicity (c) III 0.7956 79.56%
Estrogen receptor binding - 0.7531 75.31%
Androgen receptor binding - 0.8170 81.70%
Thyroid receptor binding - 0.7365 73.65%
Glucocorticoid receptor binding - 0.7486 74.86%
Aromatase binding - 0.7345 73.45%
PPAR gamma - 0.7418 74.18%
Honey bee toxicity - 0.8332 83.32%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.8948 89.48%

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 93.76% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.10% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.94% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.60% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.47% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.15% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.07% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.36% 95.89%
CHEMBL2581 P07339 Cathepsin D 81.28% 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.
Fokienia hodginsii
Garcinia intermedia
Garcinia yunnanensis

Cross-Links

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PubChem 162955869
LOTUS LTS0263889
wikiData Q104944869