(20S)-3beta-[2-O-(alpha-L-Rhamnopyranosyl)-3-O-(beta-D-xylopyranosyl)-beta-D-glucopyranosyloxy]-20-hydroxydammara-24-ene-21-oic acid 2-O-(beta-D-glucopyranosyl)-6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranosyl ester

Details

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Internal ID ce300be4-4004-4e63-92c9-3e4e2fb66c93
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name [(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl] (2S)-2-hydroxy-2-[(3S,5R,8R,9R,10R,13R,14R,17S)-3-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-enoate
SMILES (Canonical) CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(=O)C(CCC=C(C)C)(C3CCC4(C3CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC(=O)[C@](CCC=C(C)C)([C@H]3CC[C@@]4([C@@H]3CC[C@H]5[C@]4(CC[C@@H]6[C@@]5(CC[C@@H](C6(C)C)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O)O[C@H]8[C@@H]([C@H]([C@@H](CO8)O)O)O)O[C@H]9[C@@H]([C@@H]([C@H]([C@@H](O9)C)O)O)O)C)C)C)O)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O)O)O)O)O)O
InChI InChI=1S/C65H108O31/c1-25(2)11-10-17-65(84,60(83)96-58-52(94-57-50(82)45(77)40(72)31(21-66)89-57)46(78)41(73)33(91-58)24-86-54-48(80)43(75)37(69)26(3)87-54)29-14-19-63(8)28(29)12-13-35-62(7)18-16-36(61(5,6)34(62)15-20-64(35,63)9)92-59-53(95-56-49(81)44(76)38(70)27(4)88-56)51(42(74)32(22-67)90-59)93-55-47(79)39(71)30(68)23-85-55/h11,26-59,66-82,84H,10,12-24H2,1-9H3/t26-,27-,28+,29-,30+,31+,32+,33+,34-,35+,36-,37-,38-,39-,40+,41+,42+,43+,44+,45-,46-,47+,48+,49+,50+,51-,52+,53+,54+,55-,56-,57-,58-,59-,62-,63+,64+,65-/m0/s1
InChI Key TUSHGITUXWESKG-OONNXCBNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C65H108O31
Molecular Weight 1385.50 g/mol
Exact Mass 1384.6874566 g/mol
Topological Polar Surface Area (TPSA) 492.00 Ų
XlogP -1.50
Atomic LogP (AlogP) -4.33
H-Bond Acceptor 31
H-Bond Donor 18
Rotatable Bonds 19

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (20S)-3beta-[2-O-(alpha-L-Rhamnopyranosyl)-3-O-(beta-D-xylopyranosyl)-beta-D-glucopyranosyloxy]-20-hydroxydammara-24-ene-21-oic acid 2-O-(beta-D-glucopyranosyl)-6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranosyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7719 77.19%
Caco-2 - 0.8780 87.80%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.8134 81.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7898 78.98%
OATP1B3 inhibitior - 0.2428 24.28%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6776 67.76%
BSEP inhibitior + 0.9341 93.41%
P-glycoprotein inhibitior + 0.7456 74.56%
P-glycoprotein substrate + 0.5479 54.79%
CYP3A4 substrate + 0.7501 75.01%
CYP2C9 substrate - 0.7973 79.73%
CYP2D6 substrate - 0.8649 86.49%
CYP3A4 inhibition - 0.9469 94.69%
CYP2C9 inhibition - 0.8637 86.37%
CYP2C19 inhibition - 0.9118 91.18%
CYP2D6 inhibition - 0.9391 93.91%
CYP1A2 inhibition - 0.9069 90.69%
CYP2C8 inhibition + 0.7649 76.49%
CYP inhibitory promiscuity - 0.9514 95.14%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6516 65.16%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.8982 89.82%
Skin irritation - 0.5512 55.12%
Skin corrosion - 0.9480 94.80%
Ames mutagenesis - 0.6154 61.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7937 79.37%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.6372 63.72%
skin sensitisation - 0.9013 90.13%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.9325 93.25%
Acute Oral Toxicity (c) I 0.4409 44.09%
Estrogen receptor binding + 0.7640 76.40%
Androgen receptor binding + 0.7560 75.60%
Thyroid receptor binding + 0.6383 63.83%
Glucocorticoid receptor binding + 0.8170 81.70%
Aromatase binding + 0.6693 66.93%
PPAR gamma + 0.8307 83.07%
Honey bee toxicity - 0.5888 58.88%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9413 94.13%

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 99.19% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.50% 96.09%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 94.87% 91.24%
CHEMBL325 Q13547 Histone deacetylase 1 94.62% 95.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.84% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 93.20% 94.75%
CHEMBL3714130 P46095 G-protein coupled receptor 6 92.38% 97.36%
CHEMBL233 P35372 Mu opioid receptor 92.31% 97.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.75% 97.09%
CHEMBL2581 P07339 Cathepsin D 91.18% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.81% 89.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 88.29% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 87.67% 95.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.67% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.55% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.27% 94.45%
CHEMBL5255 O00206 Toll-like receptor 4 86.99% 92.50%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 86.16% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.63% 99.17%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.56% 92.88%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.40% 95.89%
CHEMBL5028 O14672 ADAM10 83.52% 97.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.78% 92.94%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.48% 90.08%
CHEMBL218 P21554 Cannabinoid CB1 receptor 82.35% 96.61%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.85% 92.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.36% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.56% 100.00%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 80.49% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.44% 93.04%

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.
Coleostephus myconis
Dahlia pinnata
Gynostemma pentaphyllum
Synotis alata

Cross-Links

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PubChem 46845275
NPASS NPC157558