(3S,8R,9R,10R)-heptadec-1-en-4,6-diyne-3,8,9,10-tetrol

Details

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Internal ID 07b8a695-233e-4712-ac11-6267ba6d24db
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (3S,8R,9R,10R)-heptadec-1-en-4,6-diyne-3,8,9,10-tetrol
SMILES (Canonical) CCCCCCCC(C(C(C#CC#CC(C=C)O)O)O)O
SMILES (Isomeric) CCCCCCC[C@H]([C@H]([C@@H](C#CC#C[C@H](C=C)O)O)O)O
InChI InChI=1S/C17H26O4/c1-3-5-6-7-8-12-15(19)17(21)16(20)13-10-9-11-14(18)4-2/h4,14-21H,2-3,5-8,12H2,1H3/t14-,15+,16+,17+/m0/s1
InChI Key MMVNLSXYHISWMN-YLFCFFPRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H26O4
Molecular Weight 294.40 g/mol
Exact Mass 294.18310931 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 2.40
Atomic LogP (AlogP) 0.98
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,8R,9R,10R)-heptadec-1-en-4,6-diyne-3,8,9,10-tetrol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7859 78.59%
Caco-2 - 0.7379 73.79%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.5014 50.14%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9131 91.31%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9088 90.88%
BSEP inhibitior - 0.9389 93.89%
P-glycoprotein inhibitior - 0.8948 89.48%
P-glycoprotein substrate - 0.7640 76.40%
CYP3A4 substrate - 0.5222 52.22%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate - 0.7498 74.98%
CYP3A4 inhibition - 0.6083 60.83%
CYP2C9 inhibition - 0.8071 80.71%
CYP2C19 inhibition - 0.7565 75.65%
CYP2D6 inhibition - 0.8511 85.11%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.8248 82.48%
CYP inhibitory promiscuity - 0.8203 82.03%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.6970 69.70%
Eye corrosion - 0.9468 94.68%
Eye irritation - 0.9347 93.47%
Skin irritation - 0.6274 62.74%
Skin corrosion - 0.9098 90.98%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7014 70.14%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.5276 52.76%
skin sensitisation - 0.6048 60.48%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.9004 90.04%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.6219 62.19%
Acute Oral Toxicity (c) III 0.4646 46.46%
Estrogen receptor binding + 0.6605 66.05%
Androgen receptor binding - 0.6476 64.76%
Thyroid receptor binding + 0.7160 71.60%
Glucocorticoid receptor binding + 0.6985 69.85%
Aromatase binding + 0.5855 58.55%
PPAR gamma + 0.5624 56.24%
Honey bee toxicity - 0.9259 92.59%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6213 62.13%
Fish aquatic toxicity + 0.9568 95.68%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 96.24% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 95.18% 92.86%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 95.16% 85.94%
CHEMBL2581 P07339 Cathepsin D 95.08% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 91.34% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.02% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.57% 92.08%
CHEMBL2885 P07451 Carbonic anhydrase III 89.87% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.13% 99.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.64% 91.81%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.06% 95.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.15% 93.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.99% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 83.02% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.85% 91.11%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.24% 100.00%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 81.35% 85.40%
CHEMBL2996 Q05655 Protein kinase C delta 80.96% 97.79%

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.
Hydrocotyle leucocephala

Cross-Links

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PubChem 163090813
LOTUS LTS0229814
wikiData Q105168119