(E,3R,10S)-dodec-4-en-6,8-diyne-1,3,10-triol

Details

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Internal ID e9bec6c4-bd28-4ad0-ad04-b72dfdc51706
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (E,3R,10S)-dodec-4-en-6,8-diyne-1,3,10-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O3/c1-2-11(14)7-5-3-4-6-8-12(15)9-10-13/h6,8,11-15H,2,9-10H2,1H3/b8-6+/t11-,12-/m0/s1
InChI Key FRCQILBDHYIEHQ-BIVWETNQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O3
Molecular Weight 208.25 g/mol
Exact Mass 208.109944368 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.06
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 (E,3R,10S)-dodec-4-en-6,8-diyne-1,3,10-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9488 94.88%
Caco-2 - 0.8040 80.40%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5864 58.64%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.8711 87.11%
OATP1B3 inhibitior + 0.9535 95.35%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8588 85.88%
BSEP inhibitior - 0.9310 93.10%
P-glycoprotein inhibitior - 0.9760 97.60%
P-glycoprotein substrate - 0.8266 82.66%
CYP3A4 substrate - 0.5994 59.94%
CYP2C9 substrate - 0.8056 80.56%
CYP2D6 substrate - 0.7828 78.28%
CYP3A4 inhibition - 0.7476 74.76%
CYP2C9 inhibition - 0.8651 86.51%
CYP2C19 inhibition - 0.8069 80.69%
CYP2D6 inhibition - 0.9078 90.78%
CYP1A2 inhibition - 0.6234 62.34%
CYP2C8 inhibition - 0.9349 93.49%
CYP inhibitory promiscuity - 0.6763 67.63%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.6798 67.98%
Eye corrosion - 0.7941 79.41%
Eye irritation - 0.9582 95.82%
Skin irritation - 0.5401 54.01%
Skin corrosion - 0.6976 69.76%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5606 56.06%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5606 56.06%
skin sensitisation - 0.8200 82.00%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.6176 61.76%
Acute Oral Toxicity (c) IV 0.3906 39.06%
Estrogen receptor binding + 0.6428 64.28%
Androgen receptor binding - 0.8241 82.41%
Thyroid receptor binding + 0.6586 65.86%
Glucocorticoid receptor binding + 0.6912 69.12%
Aromatase binding - 0.5070 50.70%
PPAR gamma + 0.5753 57.53%
Honey bee toxicity - 0.8728 87.28%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.9240 92.40%

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 93.34% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.02% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.58% 99.17%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.13% 93.10%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.27% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.26% 96.61%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.26% 92.86%

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.
Doronicum pardalianches
Emilia sonchifolia
Osteospermum imbricatum

Cross-Links

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PubChem 162845538
LOTUS LTS0160692
wikiData Q105306842