4-Ethenyl-5-methyl-2-methylidenehex-5-ene-1,3-diol

Details

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Internal ID f2d90edb-2489-4625-b3ba-4c06504231cb
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 4-ethenyl-5-methyl-2-methylidenehex-5-ene-1,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O2/c1-5-9(7(2)3)10(12)8(4)6-11/h5,9-12H,1-2,4,6H2,3H3
InChI Key VYMSAJDGBJPIAV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O2
Molecular Weight 168.23 g/mol
Exact Mass 168.115029749 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.27
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Ethenyl-5-methyl-2-methylidenehex-5-ene-1,3-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9606 96.06%
Caco-2 - 0.7964 79.64%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.4497 44.97%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9362 93.62%
OATP1B3 inhibitior + 0.9603 96.03%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8838 88.38%
BSEP inhibitior - 0.9642 96.42%
P-glycoprotein inhibitior - 0.9516 95.16%
P-glycoprotein substrate - 0.9356 93.56%
CYP3A4 substrate - 0.6520 65.20%
CYP2C9 substrate - 0.8172 81.72%
CYP2D6 substrate - 0.7743 77.43%
CYP3A4 inhibition - 0.8443 84.43%
CYP2C9 inhibition - 0.8417 84.17%
CYP2C19 inhibition - 0.7769 77.69%
CYP2D6 inhibition - 0.9221 92.21%
CYP1A2 inhibition - 0.6870 68.70%
CYP2C8 inhibition - 0.9627 96.27%
CYP inhibitory promiscuity - 0.6342 63.42%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.7012 70.12%
Eye corrosion + 0.4585 45.85%
Eye irritation + 0.8300 83.00%
Skin irritation + 0.4927 49.27%
Skin corrosion - 0.6458 64.58%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6989 69.89%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.7093 70.93%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6701 67.01%
Acute Oral Toxicity (c) II 0.4152 41.52%
Estrogen receptor binding - 0.7733 77.33%
Androgen receptor binding - 0.9002 90.02%
Thyroid receptor binding - 0.6195 61.95%
Glucocorticoid receptor binding - 0.8553 85.53%
Aromatase binding - 0.7985 79.85%
PPAR gamma - 0.7936 79.36%
Honey bee toxicity - 0.7773 77.73%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.9400 94.00%
Fish aquatic toxicity - 0.6892 68.92%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.57% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.41% 91.11%
CHEMBL2885 P07451 Carbonic anhydrase III 87.39% 87.45%
CHEMBL2581 P07339 Cathepsin D 84.31% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.42% 97.29%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.54% 85.14%

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 herba-alba
Hofmeisteria schaffneri

Cross-Links

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PubChem 14705672
LOTUS LTS0248945
wikiData Q104074043