6-(Hydroxymethyl)hept-6-ene-2,5-dione

Details

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Internal ID 2089c18a-6b76-4e29-99ce-6788b02ed556
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 6-(hydroxymethyl)hept-6-ene-2,5-dione
SMILES (Canonical) CC(=O)CCC(=O)C(=C)CO
SMILES (Isomeric) CC(=O)CCC(=O)C(=C)CO
InChI InChI=1S/C8H12O3/c1-6(5-9)8(11)4-3-7(2)10/h9H,1,3-5H2,2H3
InChI Key OUWAGQDIAXXNBV-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C8H12O3
Molecular Weight 156.18 g/mol
Exact Mass 156.078644241 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP -0.70
Atomic LogP (AlogP) 0.47
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(Hydroxymethyl)hept-6-ene-2,5-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9713 97.13%
Caco-2 + 0.7376 73.76%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7870 78.70%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.9424 94.24%
OATP1B3 inhibitior + 0.9530 95.30%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9339 93.39%
P-glycoprotein inhibitior - 0.9692 96.92%
P-glycoprotein substrate - 0.9646 96.46%
CYP3A4 substrate - 0.6924 69.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8305 83.05%
CYP3A4 inhibition - 0.8343 83.43%
CYP2C9 inhibition - 0.8269 82.69%
CYP2C19 inhibition - 0.8293 82.93%
CYP2D6 inhibition - 0.8842 88.42%
CYP1A2 inhibition - 0.6882 68.82%
CYP2C8 inhibition - 0.9894 98.94%
CYP inhibitory promiscuity - 0.8895 88.95%
UGT catelyzed - 0.5638 56.38%
Carcinogenicity (binary) - 0.6423 64.23%
Carcinogenicity (trinary) Non-required 0.6934 69.34%
Eye corrosion - 0.6084 60.84%
Eye irritation + 0.9369 93.69%
Skin irritation + 0.5607 56.07%
Skin corrosion - 0.9106 91.06%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7371 73.71%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.6841 68.41%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.6158 61.58%
Acute Oral Toxicity (c) III 0.6227 62.27%
Estrogen receptor binding - 0.9573 95.73%
Androgen receptor binding - 0.9026 90.26%
Thyroid receptor binding - 0.8755 87.55%
Glucocorticoid receptor binding - 0.9201 92.01%
Aromatase binding - 0.8714 87.14%
PPAR gamma - 0.8102 81.02%
Honey bee toxicity - 0.9454 94.54%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.9352 93.52%

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 92.28% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.88% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.48% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.24% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 80.33% 91.19%

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.
Chrysothamnus viscidiflorus

Cross-Links

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PubChem 16085190
LOTUS LTS0049719
wikiData Q105200488