(8R,9R,10R)-heptadec-1-en-11,13-diyne-8,9,10-triol

Details

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Internal ID 291061fb-7194-43be-86a5-928a934c89ae
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (8R,9R,10R)-heptadec-1-en-11,13-diyne-8,9,10-triol
SMILES (Canonical) CCCC#CC#CC(C(C(CCCCCC=C)O)O)O
SMILES (Isomeric) CCCC#CC#C[C@H]([C@@H]([C@@H](CCCCCC=C)O)O)O
InChI InChI=1S/C17H26O3/c1-3-5-7-9-11-13-15(18)17(20)16(19)14-12-10-8-6-4-2/h3,15-20H,1,4-7,9,11,13H2,2H3/t15-,16-,17-/m1/s1
InChI Key VTJDJUWUGQEKRI-BRWVUGGUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H26O3
Molecular Weight 278.40 g/mol
Exact Mass 278.18819469 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.01
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8R,9R,10R)-heptadec-1-en-11,13-diyne-8,9,10-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8484 84.84%
Caco-2 - 0.6456 64.56%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.5312 53.12%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9108 91.08%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8838 88.38%
BSEP inhibitior - 0.8618 86.18%
P-glycoprotein inhibitior - 0.9297 92.97%
P-glycoprotein substrate - 0.7388 73.88%
CYP3A4 substrate + 0.5146 51.46%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate - 0.7498 74.98%
CYP3A4 inhibition - 0.7411 74.11%
CYP2C9 inhibition - 0.7826 78.26%
CYP2C19 inhibition - 0.7538 75.38%
CYP2D6 inhibition - 0.8712 87.12%
CYP1A2 inhibition - 0.5564 55.64%
CYP2C8 inhibition - 0.7496 74.96%
CYP inhibitory promiscuity - 0.8032 80.32%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6450 64.50%
Eye corrosion - 0.8771 87.71%
Eye irritation - 0.9020 90.20%
Skin irritation - 0.6216 62.16%
Skin corrosion - 0.8539 85.39%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6619 66.19%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.5787 57.87%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.9098 90.98%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5400 54.00%
Acute Oral Toxicity (c) IV 0.3727 37.27%
Estrogen receptor binding + 0.7289 72.89%
Androgen receptor binding - 0.5971 59.71%
Thyroid receptor binding + 0.5880 58.80%
Glucocorticoid receptor binding + 0.5964 59.64%
Aromatase binding + 0.5325 53.25%
PPAR gamma + 0.6320 63.20%
Honey bee toxicity - 0.8660 86.60%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5124 51.24%
Fish aquatic toxicity + 0.8638 86.38%

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
CHEMBL2581 P07339 Cathepsin D 95.46% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.50% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 93.04% 90.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.60% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.97% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.28% 99.17%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 88.27% 85.40%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 85.58% 85.94%
CHEMBL2885 P07451 Carbonic anhydrase III 85.08% 87.45%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.59% 96.47%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.26% 94.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.15% 92.08%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.57% 93.56%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.43% 95.17%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 82.37% 97.34%
CHEMBL1907 P15144 Aminopeptidase N 81.71% 93.31%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.99% 100.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.96% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.64% 96.00%
CHEMBL242 Q92731 Estrogen receptor beta 80.58% 98.35%

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.
Cirsium japonicum

Cross-Links

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PubChem 162905802
LOTUS LTS0216823
wikiData Q105292765