4-(Hydroxymethyl)octa-3,5-diene-2,7-diol

Details

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Internal ID eec090dc-307a-463b-9fa4-1937c3090614
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 4-(hydroxymethyl)octa-3,5-diene-2,7-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H16O3/c1-7(11)3-4-9(6-10)5-8(2)12/h3-5,7-8,10-12H,6H2,1-2H3
InChI Key KWETYTFGFLMCQO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16O3
Molecular Weight 172.22 g/mol
Exact Mass 172.109944368 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.22
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(Hydroxymethyl)octa-3,5-diene-2,7-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9623 96.23%
Caco-2 + 0.7207 72.07%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5870 58.70%
OATP2B1 inhibitior - 0.8635 86.35%
OATP1B1 inhibitior + 0.9264 92.64%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9517 95.17%
P-glycoprotein inhibitior - 0.9788 97.88%
P-glycoprotein substrate - 0.9464 94.64%
CYP3A4 substrate - 0.6774 67.74%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7901 79.01%
CYP3A4 inhibition - 0.7100 71.00%
CYP2C9 inhibition - 0.8321 83.21%
CYP2C19 inhibition - 0.7916 79.16%
CYP2D6 inhibition - 0.8991 89.91%
CYP1A2 inhibition - 0.8242 82.42%
CYP2C8 inhibition - 0.9690 96.90%
CYP inhibitory promiscuity - 0.5601 56.01%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5640 56.40%
Carcinogenicity (trinary) Non-required 0.6678 66.78%
Eye corrosion - 0.6329 63.29%
Eye irritation - 0.5080 50.80%
Skin irritation - 0.5597 55.97%
Skin corrosion - 0.6395 63.95%
Ames mutagenesis - 0.7083 70.83%
Human Ether-a-go-go-Related Gene inhibition - 0.6901 69.01%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5053 50.53%
skin sensitisation - 0.5385 53.85%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.4743 47.43%
Acute Oral Toxicity (c) III 0.6581 65.81%
Estrogen receptor binding - 0.9122 91.22%
Androgen receptor binding - 0.9162 91.62%
Thyroid receptor binding - 0.7805 78.05%
Glucocorticoid receptor binding - 0.7422 74.22%
Aromatase binding - 0.8615 86.15%
PPAR gamma - 0.8346 83.46%
Honey bee toxicity - 0.9109 91.09%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.9500 95.00%
Fish aquatic toxicity - 0.6649 66.49%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.98% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.29% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.57% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.09% 97.29%
CHEMBL226 P30542 Adenosine A1 receptor 81.48% 95.93%
CHEMBL2885 P07451 Carbonic anhydrase III 80.90% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.62% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162971763
LOTUS LTS0093501
wikiData Q104170650