(2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,8R,10S,11S,12S,14S,15R,16R)-10,14-dihydroxy-7,7,12,16-tetramethyl-15-[(2R,5R,6S)-5,6,7-trihydroxy-6-methylheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID 04b0a82f-4c1a-43cf-8779-e1db1a8de02a
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins > Cucurbitacin glycosides
IUPAC Name (2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,8R,10S,11S,12S,14S,15R,16R)-10,14-dihydroxy-7,7,12,16-tetramethyl-15-[(2R,5R,6S)-5,6,7-trihydroxy-6-methylheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H62O11/c1-18(7-8-23(41)34(6,45)17-38)25-20(40)14-33(5)29-19(39)13-22-31(2,3)24(47-30-28(44)27(43)26(42)21(15-37)46-30)9-10-35(22)16-36(29,35)12-11-32(25,33)4/h18-30,37-45H,7-17H2,1-6H3/t18-,19+,20+,21-,22+,23-,24+,25+,26-,27+,28-,29+,30+,32-,33+,34+,35-,36+/m1/s1
InChI Key PQMDZXOZFXZRLE-WQCSCSKNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H62O11
Molecular Weight 670.90 g/mol
Exact Mass 670.42921279 g/mol
Topological Polar Surface Area (TPSA) 201.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.07
H-Bond Acceptor 11
H-Bond Donor 9
Rotatable Bonds 9

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-[[(1S,3R,6S,8R,10S,11S,12S,14S,15R,16R)-10,14-dihydroxy-7,7,12,16-tetramethyl-15-[(2R,5R,6S)-5,6,7-trihydroxy-6-methylheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]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 + 0.5937 59.37%
Caco-2 - 0.8546 85.46%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.5869 58.69%
OATP2B1 inhibitior - 0.7213 72.13%
OATP1B1 inhibitior + 0.8221 82.21%
OATP1B3 inhibitior + 0.9226 92.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8818 88.18%
P-glycoprotein inhibitior + 0.7114 71.14%
P-glycoprotein substrate - 0.5780 57.80%
CYP3A4 substrate + 0.7132 71.32%
CYP2C9 substrate - 0.8018 80.18%
CYP2D6 substrate - 0.8301 83.01%
CYP3A4 inhibition - 0.9159 91.59%
CYP2C9 inhibition - 0.7399 73.99%
CYP2C19 inhibition - 0.7886 78.86%
CYP2D6 inhibition - 0.9500 95.00%
CYP1A2 inhibition - 0.8589 85.89%
CYP2C8 inhibition + 0.5897 58.97%
CYP inhibitory promiscuity - 0.9556 95.56%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7201 72.01%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9171 91.71%
Skin irritation - 0.7128 71.28%
Skin corrosion - 0.9478 94.78%
Ames mutagenesis - 0.7170 71.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6943 69.43%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.7874 78.74%
skin sensitisation - 0.9054 90.54%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.7021 70.21%
Acute Oral Toxicity (c) I 0.5222 52.22%
Estrogen receptor binding + 0.5988 59.88%
Androgen receptor binding + 0.7587 75.87%
Thyroid receptor binding - 0.5671 56.71%
Glucocorticoid receptor binding + 0.5378 53.78%
Aromatase binding + 0.6604 66.04%
PPAR gamma + 0.6199 61.99%
Honey bee toxicity - 0.6664 66.64%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.8276 82.76%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.59% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.65% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.75% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.98% 97.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 94.53% 95.58%
CHEMBL2996 Q05655 Protein kinase C delta 94.44% 97.79%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.73% 85.14%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 91.97% 92.88%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 91.71% 100.00%
CHEMBL220 P22303 Acetylcholinesterase 91.69% 94.45%
CHEMBL218 P21554 Cannabinoid CB1 receptor 90.14% 96.61%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.77% 97.14%
CHEMBL2581 P07339 Cathepsin D 89.68% 98.95%
CHEMBL2094135 Q96BI3 Gamma-secretase 87.54% 98.05%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.50% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.97% 94.45%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.29% 100.00%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 86.05% 82.50%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 85.92% 91.03%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 85.71% 96.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.70% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.91% 95.89%
CHEMBL284 P27487 Dipeptidyl peptidase IV 84.79% 95.69%
CHEMBL344 Q99705 Melanin-concentrating hormone receptor 1 84.50% 92.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.36% 100.00%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.70% 92.86%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.35% 89.62%
CHEMBL237 P41145 Kappa opioid receptor 83.19% 98.10%
CHEMBL259 P32245 Melanocortin receptor 4 82.73% 95.38%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 82.52% 99.17%
CHEMBL2413 P32246 C-C chemokine receptor type 1 82.47% 89.50%
CHEMBL2007625 O75874 Isocitrate dehydrogenase [NADP] cytoplasmic 82.44% 99.00%
CHEMBL1937 Q92769 Histone deacetylase 2 82.12% 94.75%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.88% 96.47%
CHEMBL226 P30542 Adenosine A1 receptor 81.67% 95.93%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.63% 91.24%
CHEMBL4581 P52732 Kinesin-like protein 1 81.35% 93.18%
CHEMBL1977 P11473 Vitamin D receptor 81.33% 99.43%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.00% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.96% 94.62%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.76% 91.07%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.12% 89.34%

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.
Tarenna gracilipes

Cross-Links

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PubChem 162996998
LOTUS LTS0051743
wikiData Q105213286