Gymnasterkoreayne C

Details

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Internal ID f160d0e7-8c1c-4c54-be08-3ae63c907f79
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name [(3S,8S,9Z)-8-hydroxyheptadeca-1,9,16-trien-4,6-diyn-3-yl] acetate
SMILES (Canonical) CC(=O)OC(C=C)C#CC#CC(C=CCCCCCC=C)O
SMILES (Isomeric) CC(=O)O[C@@H](C=C)C#CC#C[C@H](/C=C\CCCCCC=C)O
InChI InChI=1S/C19H24O3/c1-4-6-7-8-9-10-11-14-18(21)15-12-13-16-19(5-2)22-17(3)20/h4-5,11,14,18-19,21H,1-2,6-10H2,3H3/b14-11-/t18-,19-/m0/s1
InChI Key XLZZUDXEHSVXOR-ZUKORNFRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H24O3
Molecular Weight 300.40 g/mol
Exact Mass 300.17254462 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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CHEMBL463830

2D Structure

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2D Structure of Gymnasterkoreayne C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9640 96.40%
Caco-2 - 0.6964 69.64%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.6538 65.38%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.8956 89.56%
OATP1B3 inhibitior + 0.9437 94.37%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8864 88.64%
P-glycoprotein inhibitior - 0.8055 80.55%
P-glycoprotein substrate - 0.8211 82.11%
CYP3A4 substrate + 0.5546 55.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8563 85.63%
CYP3A4 inhibition - 0.8064 80.64%
CYP2C9 inhibition - 0.7719 77.19%
CYP2C19 inhibition - 0.8189 81.89%
CYP2D6 inhibition - 0.9476 94.76%
CYP1A2 inhibition - 0.7196 71.96%
CYP2C8 inhibition - 0.7585 75.85%
CYP inhibitory promiscuity - 0.7934 79.34%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6058 60.58%
Carcinogenicity (trinary) Non-required 0.6558 65.58%
Eye corrosion + 0.8895 88.95%
Eye irritation - 0.9294 92.94%
Skin irritation + 0.5086 50.86%
Skin corrosion - 0.7580 75.80%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6516 65.16%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.6308 63.08%
skin sensitisation + 0.8098 80.98%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6349 63.49%
Acute Oral Toxicity (c) III 0.6980 69.80%
Estrogen receptor binding - 0.5116 51.16%
Androgen receptor binding - 0.6102 61.02%
Thyroid receptor binding + 0.5436 54.36%
Glucocorticoid receptor binding + 0.6323 63.23%
Aromatase binding - 0.5856 58.56%
PPAR gamma + 0.5946 59.46%
Honey bee toxicity - 0.6799 67.99%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5137 51.37%
Fish aquatic toxicity + 0.9509 95.09%

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 94.57% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.42% 99.17%
CHEMBL2581 P07339 Cathepsin D 93.29% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.14% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.31% 94.45%
CHEMBL1829 O15379 Histone deacetylase 3 86.44% 95.00%
CHEMBL1937 Q92769 Histone deacetylase 2 85.03% 94.75%
CHEMBL340 P08684 Cytochrome P450 3A4 84.62% 91.19%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.88% 97.21%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.69% 97.29%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.68% 94.33%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 81.87% 92.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.84% 96.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.67% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.79% 96.00%

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.
Aster koraiensis
Baccharis thesioides
Bonnetia paniculata
Glycosmis ovoidea
Raukaua simplex
Veronica chamaedrys
Vitex agnus-castus

Cross-Links

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PubChem 11779567
NPASS NPC212730
LOTUS LTS0048866
wikiData Q105330594