(2R,3R,4S,5S,6R)-2-[[(1R,2S,5S,7R,8S,9R)-7-hydroxy-5-(2-hydroxypropan-2-yl)-2,8-dimethyl-9-tricyclo[4.4.0.02,8]decanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID db3774d7-881b-43fc-ae02-9453fcdf43d1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name (2R,3R,4S,5S,6R)-2-[[(1R,2S,5S,7R,8S,9R)-7-hydroxy-5-(2-hydroxypropan-2-yl)-2,8-dimethyl-9-tricyclo[4.4.0.02,8]decanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) CC12CCC(C3C1CC(C2(C3O)C)OC4C(C(C(C(O4)CO)O)O)O)C(C)(C)O
SMILES (Isomeric) C[C@]12CC[C@@H](C3[C@H]1C[C@H]([C@@]2([C@@H]3O)C)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)C(C)(C)O
InChI InChI=1S/C21H36O8/c1-19(2,27)9-5-6-20(3)10-7-12(21(20,4)17(26)13(9)10)29-18-16(25)15(24)14(23)11(8-22)28-18/h9-18,22-27H,5-8H2,1-4H3/t9-,10+,11+,12+,13?,14+,15-,16+,17+,18-,20-,21+/m0/s1
InChI Key FNAYTJOYVAPBEA-MXFJHXAWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H36O8
Molecular Weight 416.50 g/mol
Exact Mass 416.24101810 g/mol
Topological Polar Surface Area (TPSA) 140.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.62
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 4

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,2S,5S,7R,8S,9R)-7-hydroxy-5-(2-hydroxypropan-2-yl)-2,8-dimethyl-9-tricyclo[4.4.0.02,8]decanyl]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 + 0.5896 58.96%
Caco-2 - 0.8146 81.46%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.6884 68.84%
OATP2B1 inhibitior - 0.8615 86.15%
OATP1B1 inhibitior + 0.8438 84.38%
OATP1B3 inhibitior + 0.9034 90.34%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9480 94.80%
P-glycoprotein inhibitior - 0.8191 81.91%
P-glycoprotein substrate - 0.8787 87.87%
CYP3A4 substrate + 0.6388 63.88%
CYP2C9 substrate - 0.7983 79.83%
CYP2D6 substrate - 0.8352 83.52%
CYP3A4 inhibition - 0.9315 93.15%
CYP2C9 inhibition - 0.7710 77.10%
CYP2C19 inhibition - 0.8286 82.86%
CYP2D6 inhibition - 0.9583 95.83%
CYP1A2 inhibition - 0.8112 81.12%
CYP2C8 inhibition + 0.4593 45.93%
CYP inhibitory promiscuity - 0.9296 92.96%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7415 74.15%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9633 96.33%
Skin irritation - 0.7187 71.87%
Skin corrosion - 0.9515 95.15%
Ames mutagenesis - 0.7407 74.07%
Human Ether-a-go-go-Related Gene inhibition - 0.5881 58.81%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5676 56.76%
skin sensitisation - 0.9259 92.59%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7210 72.10%
Acute Oral Toxicity (c) III 0.4267 42.67%
Estrogen receptor binding + 0.6461 64.61%
Androgen receptor binding + 0.6226 62.26%
Thyroid receptor binding + 0.5888 58.88%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.7419 74.19%
PPAR gamma + 0.5795 57.95%
Honey bee toxicity - 0.8118 81.18%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9001 90.01%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.84% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.82% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.87% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.65% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 88.05% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.47% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.03% 95.89%
CHEMBL218 P21554 Cannabinoid CB1 receptor 86.58% 96.61%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.97% 86.33%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 84.44% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.58% 93.04%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.23% 97.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.82% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.64% 86.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.57% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 80.85% 94.73%
CHEMBL226 P30542 Adenosine A1 receptor 80.56% 95.93%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.49% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.20% 92.62%

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.
Kandelia candel

Cross-Links

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PubChem 118727704
LOTUS LTS0139763
wikiData Q104998193