6-Methyl-2-methylideneoct-7-ene-1,3,6-triol

Details

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Internal ID 81e0b27d-f10a-4fc0-abff-258d9d03d6f0
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 6-methyl-2-methylideneoct-7-ene-1,3,6-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O3/c1-4-10(3,13)6-5-9(12)8(2)7-11/h4,9,11-13H,1-2,5-7H2,3H3
InChI Key FNIGDKAVQMRSAK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O3
Molecular Weight 186.25 g/mol
Exact Mass 186.125594432 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.61
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Methyl-2-methylideneoct-7-ene-1,3,6-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9339 93.39%
Caco-2 - 0.5943 59.43%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5043 50.43%
OATP2B1 inhibitior - 0.8508 85.08%
OATP1B1 inhibitior + 0.9398 93.98%
OATP1B3 inhibitior + 0.9532 95.32%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6867 68.67%
BSEP inhibitior - 0.9470 94.70%
P-glycoprotein inhibitior - 0.9759 97.59%
P-glycoprotein substrate - 0.9131 91.31%
CYP3A4 substrate - 0.5670 56.70%
CYP2C9 substrate - 0.8160 81.60%
CYP2D6 substrate - 0.7629 76.29%
CYP3A4 inhibition - 0.8930 89.30%
CYP2C9 inhibition - 0.7694 76.94%
CYP2C19 inhibition - 0.8025 80.25%
CYP2D6 inhibition - 0.8792 87.92%
CYP1A2 inhibition - 0.7308 73.08%
CYP2C8 inhibition - 0.9289 92.89%
CYP inhibitory promiscuity - 0.7969 79.69%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.6646 66.46%
Eye corrosion - 0.9224 92.24%
Eye irritation + 0.6066 60.66%
Skin irritation - 0.7010 70.10%
Skin corrosion - 0.9601 96.01%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6061 60.61%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.6870 68.70%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.4545 45.45%
Acute Oral Toxicity (c) IV 0.5036 50.36%
Estrogen receptor binding - 0.8758 87.58%
Androgen receptor binding - 0.8034 80.34%
Thyroid receptor binding - 0.7197 71.97%
Glucocorticoid receptor binding + 0.5707 57.07%
Aromatase binding - 0.7778 77.78%
PPAR gamma - 0.6983 69.83%
Honey bee toxicity - 0.8796 87.96%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity + 0.8131 81.31%

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
CHEMBL4040 P28482 MAP kinase ERK2 92.44% 83.82%
CHEMBL2581 P07339 Cathepsin D 88.42% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.34% 97.29%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 87.24% 90.93%
CHEMBL2885 P07451 Carbonic anhydrase III 86.89% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.18% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.54% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 84.53% 94.73%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.62% 96.47%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.36% 91.11%

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.
Artemisia xerophytica

Cross-Links

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PubChem 14779627
LOTUS LTS0012650
wikiData Q104998313