(2R,3R,4S,5S,6R)-2-[[(1R,2R,3R,5R,6R,8S,12S)-8,12-dihydroxy-1,5,9,9-tetramethyl-10-oxatricyclo[6.2.2.02,6]dodecan-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID fbebaa0a-e100-40f8-8845-8f55a186a3a6
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (2R,3R,4S,5S,6R)-2-[[(1R,2R,3R,5R,6R,8S,12S)-8,12-dihydroxy-1,5,9,9-tetramethyl-10-oxatricyclo[6.2.2.02,6]dodecan-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) CC1CC(C2C1CC3(C(CC2(OC3(C)C)C)O)O)OC4C(C(C(C(O4)CO)O)O)O
SMILES (Isomeric) C[C@@H]1C[C@H]([C@H]2[C@@H]1C[C@@]3([C@H](C[C@]2(OC3(C)C)C)O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
InChI InChI=1S/C21H36O9/c1-9-5-11(28-18-17(26)16(25)15(24)12(8-22)29-18)14-10(9)6-21(27)13(23)7-20(14,4)30-19(21,2)3/h9-18,22-27H,5-8H2,1-4H3/t9-,10-,11-,12-,13+,14-,15-,16+,17-,18-,20-,21+/m1/s1
InChI Key SPYAOTULQPJFGN-XUKBFMRMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H36O9
Molecular Weight 432.50 g/mol
Exact Mass 432.23593272 g/mol
Topological Polar Surface Area (TPSA) 149.00 Ų
XlogP -1.00
Atomic LogP (AlogP) -1.10
H-Bond Acceptor 9
H-Bond Donor 6
Rotatable Bonds 3

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,3R,5R,6R,8S,12S)-8,12-dihydroxy-1,5,9,9-tetramethyl-10-oxatricyclo[6.2.2.02,6]dodecan-3-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 + 0.6063 60.63%
Caco-2 - 0.8048 80.48%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.5326 53.26%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.8961 89.61%
OATP1B3 inhibitior + 0.9161 91.61%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9277 92.77%
P-glycoprotein inhibitior - 0.7810 78.10%
P-glycoprotein substrate - 0.7874 78.74%
CYP3A4 substrate + 0.6626 66.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8424 84.24%
CYP3A4 inhibition - 0.9263 92.63%
CYP2C9 inhibition - 0.8845 88.45%
CYP2C19 inhibition - 0.8952 89.52%
CYP2D6 inhibition - 0.9537 95.37%
CYP1A2 inhibition - 0.8735 87.35%
CYP2C8 inhibition - 0.6427 64.27%
CYP inhibitory promiscuity - 0.9646 96.46%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6961 69.61%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9406 94.06%
Skin irritation - 0.7341 73.41%
Skin corrosion - 0.9533 95.33%
Ames mutagenesis - 0.5678 56.78%
Human Ether-a-go-go-Related Gene inhibition - 0.5576 55.76%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.9118 91.18%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.7439 74.39%
Acute Oral Toxicity (c) I 0.4873 48.73%
Estrogen receptor binding - 0.4934 49.34%
Androgen receptor binding + 0.5671 56.71%
Thyroid receptor binding + 0.6791 67.91%
Glucocorticoid receptor binding - 0.5409 54.09%
Aromatase binding + 0.7325 73.25%
PPAR gamma + 0.6498 64.98%
Honey bee toxicity - 0.6966 69.66%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8781 87.81%

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 97.25% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.40% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.40% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.55% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.09% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.46% 96.61%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.70% 86.33%
CHEMBL226 P30542 Adenosine A1 receptor 87.56% 95.93%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 85.54% 96.21%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.42% 86.92%
CHEMBL221 P23219 Cyclooxygenase-1 84.31% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.28% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.07% 92.94%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 84.03% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 82.38% 97.79%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.34% 95.50%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.03% 91.24%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.23% 95.89%

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.
Daucus carota

Cross-Links

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PubChem 163079455
LOTUS LTS0003652
wikiData Q105257679