I'-(6"-0-myristyl-p-glucopyanosyloxy)-3,4,3', 4'-tetradehydro1,2,1',2'-tetrahydro-l-hydroxy-yl,yl-carotene

Details

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Internal ID 6e395687-83ad-450b-8fce-18d0df6d9203
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name [(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(4E,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E,28E)-31-hydroxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaen-2-yl]oxyoxan-2-yl]methyl tetradecanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C60H92O8/c1-12-13-14-15-16-17-18-19-20-21-22-43-54(61)66-46-53-55(62)56(63)57(64)58(67-53)68-60(10,11)45-30-42-52(7)40-28-38-50(5)36-26-34-48(3)32-24-23-31-47(2)33-25-35-49(4)37-27-39-51(6)41-29-44-59(8,9)65/h23-42,53,55-58,62-65H,12-22,43-46H2,1-11H3/b24-23+,33-25+,34-26+,37-27+,38-28+,41-29+,42-30+,47-31+,48-32+,49-35+,50-36+,51-39+,52-40+/t53-,55-,56+,57-,58+/m1/s1
InChI Key DKOBIKXQKYQNOO-KEPLRZDGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C60H92O8
Molecular Weight 941.40 g/mol
Exact Mass 940.67921989 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP 17.50
Atomic LogP (AlogP) 13.96
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 32

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of I'-(6"-0-myristyl-p-glucopyanosyloxy)-3,4,3', 4'-tetradehydro1,2,1',2'-tetrahydro-l-hydroxy-yl,yl-carotene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8290 82.90%
Caco-2 - 0.8561 85.61%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.8826 88.26%
OATP2B1 inhibitior - 0.5787 57.87%
OATP1B1 inhibitior + 0.8244 82.44%
OATP1B3 inhibitior + 0.8811 88.11%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6568 65.68%
BSEP inhibitior + 0.9954 99.54%
P-glycoprotein inhibitior + 0.7549 75.49%
P-glycoprotein substrate - 0.6217 62.17%
CYP3A4 substrate + 0.6762 67.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8925 89.25%
CYP3A4 inhibition - 0.7669 76.69%
CYP2C9 inhibition - 0.7369 73.69%
CYP2C19 inhibition - 0.6813 68.13%
CYP2D6 inhibition - 0.9229 92.29%
CYP1A2 inhibition - 0.8289 82.89%
CYP2C8 inhibition + 0.5418 54.18%
CYP inhibitory promiscuity - 0.9112 91.12%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6938 69.38%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9038 90.38%
Skin irritation - 0.6483 64.83%
Skin corrosion - 0.9591 95.91%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8493 84.93%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.5052 50.52%
skin sensitisation - 0.7960 79.60%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.5854 58.54%
Acute Oral Toxicity (c) III 0.6097 60.97%
Estrogen receptor binding + 0.8149 81.49%
Androgen receptor binding - 0.5143 51.43%
Thyroid receptor binding + 0.6037 60.37%
Glucocorticoid receptor binding + 0.7361 73.61%
Aromatase binding - 0.5452 54.52%
PPAR gamma + 0.7699 76.99%
Honey bee toxicity - 0.8435 84.35%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7453 74.53%
Fish aquatic toxicity + 0.9651 96.51%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 97.54% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.65% 97.25%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 96.58% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.16% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 94.71% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.08% 91.11%
CHEMBL5255 O00206 Toll-like receptor 4 93.45% 92.50%
CHEMBL218 P21554 Cannabinoid CB1 receptor 93.04% 96.61%
CHEMBL3401 O75469 Pregnane X receptor 93.00% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.91% 96.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.61% 89.34%
CHEMBL2581 P07339 Cathepsin D 91.51% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.51% 92.08%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.02% 100.00%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.53% 92.86%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.90% 86.33%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.86% 97.29%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 85.68% 82.50%
CHEMBL4227 P25090 Lipoxin A4 receptor 85.43% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.40% 93.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.38% 96.47%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 84.15% 80.33%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.68% 94.33%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.96% 91.81%
CHEMBL5957 P21589 5'-nucleotidase 81.54% 97.78%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.12% 89.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 101921513
LOTUS LTS0058836
wikiData Q104983493