(Z)-3,4-Dideuteriohex-3-en-1-ol

Details

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Internal ID e2f3720b-bd17-4d8e-aa2b-e3e3d2436131
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (Z)-3,4-dideuteriohex-3-en-1-ol
SMILES (Canonical) CCC=CCCO
SMILES (Isomeric) [2H]/C(=C(\[2H])/CCO)/CC
InChI InChI=1S/C6H12O/c1-2-3-4-5-6-7/h3-4,7H,2,5-6H2,1H3/b4-3-/i3D,4D
InChI Key UFLHIIWVXFIJGU-KKLCAENNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12O
Molecular Weight 102.17 g/mol
Exact Mass 102.101368494 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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164668-81-9
CS-T-55628

2D Structure

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2D Structure of (Z)-3,4-Dideuteriohex-3-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 + 0.9924 99.24%
Caco-2 + 0.8071 80.71%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.6115 61.15%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9240 92.40%
OATP1B3 inhibitior + 0.9315 93.15%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9400 94.00%
P-glycoprotein inhibitior - 0.9787 97.87%
P-glycoprotein substrate - 0.9514 95.14%
CYP3A4 substrate - 0.7454 74.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9236 92.36%
CYP2C9 inhibition - 0.9219 92.19%
CYP2C19 inhibition - 0.9289 92.89%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.7010 70.10%
CYP2C8 inhibition - 0.9392 93.92%
CYP inhibitory promiscuity - 0.7811 78.11%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.6514 65.14%
Eye corrosion + 0.8230 82.30%
Eye irritation + 0.9820 98.20%
Skin irritation + 0.7350 73.50%
Skin corrosion - 0.9800 98.00%
Ames mutagenesis - 0.7432 74.32%
Human Ether-a-go-go-Related Gene inhibition - 0.6206 62.06%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6121 61.21%
skin sensitisation + 0.8246 82.46%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.6038 60.38%
Acute Oral Toxicity (c) III 0.8695 86.95%
Estrogen receptor binding - 0.9316 93.16%
Androgen receptor binding - 0.8753 87.53%
Thyroid receptor binding - 0.8323 83.23%
Glucocorticoid receptor binding - 0.8976 89.76%
Aromatase binding - 0.9023 90.23%
PPAR gamma - 0.8737 87.37%
Honey bee toxicity - 0.9479 94.79%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.9400 94.00%
Fish aquatic toxicity - 0.5737 57.37%

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 84.28% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.94% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 83.54% 87.45%

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.
Capsella bursa-pastoris
Houttuynia cordata

Cross-Links

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PubChem 10261058
NPASS NPC64946