(8R,9S,10S)-10-methoxyheptadec-16-en-4,6-diyne-8,9-diol

Details

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Internal ID 2358f748-e049-4db7-ad11-58996551bcb6
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (8R,9S,10S)-10-methoxyheptadec-16-en-4,6-diyne-8,9-diol
SMILES (Canonical) CCCC#CC#CC(C(C(CCCCCC=C)OC)O)O
SMILES (Isomeric) CCCC#CC#C[C@H]([C@@H]([C@H](CCCCCC=C)OC)O)O
InChI InChI=1S/C18H28O3/c1-4-6-8-10-12-14-16(19)18(20)17(21-3)15-13-11-9-7-5-2/h5,16-20H,2,4,6-7,9,11,13,15H2,1,3H3/t16-,17+,18+/m1/s1
InChI Key LSMAUQIQTAVNFS-SQNIBIBYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H28O3
Molecular Weight 292.40 g/mol
Exact Mass 292.20384475 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 3.80
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8R,9S,10S)-10-methoxyheptadec-16-en-4,6-diyne-8,9-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9431 94.31%
Caco-2 + 0.5504 55.04%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.5992 59.92%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9069 90.69%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8677 86.77%
P-glycoprotein inhibitior - 0.8891 88.91%
P-glycoprotein substrate - 0.6589 65.89%
CYP3A4 substrate + 0.5635 56.35%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.7572 75.72%
CYP3A4 inhibition - 0.7048 70.48%
CYP2C9 inhibition - 0.7883 78.83%
CYP2C19 inhibition - 0.7089 70.89%
CYP2D6 inhibition - 0.8687 86.87%
CYP1A2 inhibition - 0.5193 51.93%
CYP2C8 inhibition - 0.6549 65.49%
CYP inhibitory promiscuity - 0.7520 75.20%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7023 70.23%
Carcinogenicity (trinary) Non-required 0.6947 69.47%
Eye corrosion - 0.8840 88.40%
Eye irritation - 0.9350 93.50%
Skin irritation - 0.7802 78.02%
Skin corrosion - 0.9498 94.98%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6643 66.43%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5941 59.41%
skin sensitisation + 0.5759 57.59%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.8405 84.05%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5841 58.41%
Acute Oral Toxicity (c) III 0.5183 51.83%
Estrogen receptor binding + 0.8411 84.11%
Androgen receptor binding - 0.5673 56.73%
Thyroid receptor binding + 0.6926 69.26%
Glucocorticoid receptor binding + 0.6835 68.35%
Aromatase binding - 0.5477 54.77%
PPAR gamma - 0.5652 56.52%
Honey bee toxicity - 0.7521 75.21%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5176 51.76%
Fish aquatic toxicity + 0.9491 94.91%

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 96.35% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.79% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 93.29% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.51% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.02% 92.86%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.64% 94.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.89% 97.29%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.55% 96.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 86.28% 95.17%
CHEMBL2885 P07451 Carbonic anhydrase III 86.27% 87.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.04% 92.08%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 85.77% 85.40%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.67% 91.11%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.08% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.94% 93.56%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.39% 91.81%
CHEMBL1907 P15144 Aminopeptidase N 80.68% 93.31%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 80.38% 85.94%

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 163054613
LOTUS LTS0012046
wikiData Q105156613