(2R,3R,4S,5S,6R)-2-[(1R,2R)-1,5-bis(3,4-dimethoxyphenyl)-1-hydroxypent-4-yn-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID 73c40b6d-4d1c-4b95-8c76-a55e6b303bd1
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl glycosides > Fatty acyl glycosides of mono- and disaccharides
IUPAC Name (2R,3R,4S,5S,6R)-2-[(1R,2R)-1,5-bis(3,4-dimethoxyphenyl)-1-hydroxypent-4-yn-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) COC1=C(C=C(C=C1)C#CCC(C(C2=CC(=C(C=C2)OC)OC)O)OC3C(C(C(C(O3)CO)O)O)O)OC
SMILES (Isomeric) COC1=C(C=C(C=C1)C#CC[C@H]([C@@H](C2=CC(=C(C=C2)OC)OC)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)OC
InChI InChI=1S/C27H34O11/c1-33-17-10-8-15(12-20(17)35-3)6-5-7-19(23(29)16-9-11-18(34-2)21(13-16)36-4)37-27-26(32)25(31)24(30)22(14-28)38-27/h8-13,19,22-32H,7,14H2,1-4H3/t19-,22-,23-,24-,25+,26-,27-/m1/s1
InChI Key IKIFYAWQFDKTCM-OHGANORHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H34O11
Molecular Weight 534.60 g/mol
Exact Mass 534.21011190 g/mol
Topological Polar Surface Area (TPSA) 157.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.38
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R,4S,5S,6R)-2-[(1R,2R)-1,5-bis(3,4-dimethoxyphenyl)-1-hydroxypent-4-yn-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8307 83.07%
Caco-2 - 0.8540 85.40%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6151 61.51%
OATP2B1 inhibitior - 0.8616 86.16%
OATP1B1 inhibitior + 0.8611 86.11%
OATP1B3 inhibitior + 0.9405 94.05%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6827 68.27%
P-glycoprotein inhibitior - 0.4444 44.44%
P-glycoprotein substrate - 0.6282 62.82%
CYP3A4 substrate + 0.5653 56.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7833 78.33%
CYP3A4 inhibition - 0.6832 68.32%
CYP2C9 inhibition - 0.8763 87.63%
CYP2C19 inhibition - 0.8514 85.14%
CYP2D6 inhibition - 0.8970 89.70%
CYP1A2 inhibition - 0.8293 82.93%
CYP2C8 inhibition + 0.4880 48.80%
CYP inhibitory promiscuity - 0.6366 63.66%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6882 68.82%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9348 93.48%
Skin irritation - 0.8610 86.10%
Skin corrosion - 0.9548 95.48%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7967 79.67%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation - 0.8923 89.23%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.8950 89.50%
Acute Oral Toxicity (c) III 0.7317 73.17%
Estrogen receptor binding + 0.7917 79.17%
Androgen receptor binding + 0.6010 60.10%
Thyroid receptor binding + 0.6485 64.85%
Glucocorticoid receptor binding + 0.5544 55.44%
Aromatase binding + 0.5352 53.52%
PPAR gamma + 0.6595 65.95%
Honey bee toxicity - 0.7676 76.76%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.7117 71.17%

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 98.43% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.64% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.74% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.51% 96.00%
CHEMBL2581 P07339 Cathepsin D 90.40% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.24% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 88.40% 90.20%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.17% 89.62%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.10% 86.92%
CHEMBL4208 P20618 Proteasome component C5 87.99% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.65% 86.33%
CHEMBL2535 P11166 Glucose transporter 86.67% 98.75%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.11% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.34% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 84.86% 94.73%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 82.08% 100.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.21% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.78% 92.94%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.41% 97.36%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.28% 94.45%

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 163036222
LOTUS LTS0231609
wikiData Q105114643