3beta-(2-O,4-O-Di-alpha-L-rhamnopyranosyl-beta-D-glucopyranosyloxy)-16alpha-methoxypregna-5-ene-20-one

Details

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Internal ID 98167131-3118-4ee1-9eb6-906394671306
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides
IUPAC Name 1-[(3S,8S,9S,10R,13S,14S,16R,17R)-3-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-3,5-bis[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]oxan-2-yl]oxy-16-methoxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone
SMILES (Canonical) CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC(C7C(=O)C)OC)C)C)CO)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)O[C@H]3[C@@H]([C@@H]([C@H]([C@@H](O3)C)O)O)O)O[C@H]4CC[C@@]5([C@H]6CC[C@]7([C@H]([C@@H]6CC=C5C4)C[C@H]([C@@H]7C(=O)C)OC)C)C)CO)O)O)O
InChI InChI=1S/C40H64O16/c1-16(42)26-24(50-6)14-23-21-8-7-19-13-20(9-11-39(19,4)22(21)10-12-40(23,26)5)53-38-35(56-37-32(48)30(46)28(44)18(3)52-37)33(49)34(25(15-41)54-38)55-36-31(47)29(45)27(43)17(2)51-36/h7,17-18,20-38,41,43-49H,8-15H2,1-6H3/t17-,18-,20-,21+,22-,23-,24+,25+,26-,27-,28-,29+,30+,31+,32+,33-,34+,35+,36-,37-,38+,39-,40-/m0/s1
InChI Key OVNISBFHKJPJTA-KZADIOTQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C40H64O16
Molecular Weight 800.90 g/mol
Exact Mass 800.41943595 g/mol
Topological Polar Surface Area (TPSA) 244.00 Ų
XlogP -0.90
Atomic LogP (AlogP) -0.33
H-Bond Acceptor 16
H-Bond Donor 8
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3beta-(2-O,4-O-Di-alpha-L-rhamnopyranosyl-beta-D-glucopyranosyloxy)-16alpha-methoxypregna-5-ene-20-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7707 77.07%
Caco-2 - 0.8828 88.28%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.7935 79.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9015 90.15%
OATP1B3 inhibitior + 0.8836 88.36%
MATE1 inhibitior - 0.9812 98.12%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6512 65.12%
P-glycoprotein inhibitior + 0.7114 71.14%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.7534 75.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8635 86.35%
CYP3A4 inhibition - 0.9459 94.59%
CYP2C9 inhibition - 0.9388 93.88%
CYP2C19 inhibition - 0.9340 93.40%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition - 0.8591 85.91%
CYP2C8 inhibition + 0.6524 65.24%
CYP inhibitory promiscuity - 0.9017 90.17%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5818 58.18%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9195 91.95%
Skin irritation + 0.5059 50.59%
Skin corrosion - 0.9460 94.60%
Ames mutagenesis - 0.8937 89.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7488 74.88%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.8750 87.50%
skin sensitisation - 0.9115 91.15%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.8734 87.34%
Acute Oral Toxicity (c) III 0.4602 46.02%
Estrogen receptor binding + 0.8220 82.20%
Androgen receptor binding + 0.6954 69.54%
Thyroid receptor binding - 0.5557 55.57%
Glucocorticoid receptor binding + 0.6047 60.47%
Aromatase binding + 0.6776 67.76%
PPAR gamma + 0.6827 68.27%
Honey bee toxicity - 0.6273 62.73%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5855 58.55%
Fish aquatic toxicity + 0.9175 91.75%

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 99.17% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.97% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 92.38% 95.93%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 91.60% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.65% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.39% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.61% 97.09%
CHEMBL2581 P07339 Cathepsin D 88.12% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.14% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.63% 94.00%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 86.10% 89.05%
CHEMBL5255 O00206 Toll-like receptor 4 85.87% 92.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.43% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.99% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.74% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.52% 95.89%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.40% 97.36%
CHEMBL5028 O14672 ADAM10 81.67% 97.50%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.77% 97.33%

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.
Dioscorea futschauensis
Phragmites australis

Cross-Links

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PubChem 101258442
NPASS NPC153774
LOTUS LTS0078502
wikiData Q105200871