Bryonioside B

Details

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Internal ID 4968fbe6-9a7d-4a02-8649-f164a18f1851
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins > Cucurbitacin glycosides
IUPAC Name (3S,8S,9R,10R,13R,14S,17R)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-17-[(2R,5R)-5,6-dihydroxy-6-methylheptan-2-yl]-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H70O13/c1-20(10-14-27(44)39(5,6)51)22-16-17-40(7)26-13-11-23-24(42(26,9)28(45)18-41(22,40)8)12-15-29(38(23,3)4)54-37-35(33(49)31(47)25(19-43)53-37)55-36-34(50)32(48)30(46)21(2)52-36/h11,20-22,24-27,29-37,43-44,46-51H,10,12-19H2,1-9H3/t20-,21+,22-,24-,25-,26+,27-,29+,30+,31-,32-,33+,34-,35-,36+,37+,40+,41-,42+/m1/s1
InChI Key BQYXEGPEDSNOPN-UEOQDMPUSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C42H70O13
Molecular Weight 783.00 g/mol
Exact Mass 782.48164228 g/mol
Topological Polar Surface Area (TPSA) 216.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 13
H-Bond Donor 8
Rotatable Bonds 10

Synonyms

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CHEMBL464459

2D Structure

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2D Structure of Bryonioside B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8800 88.00%
Caco-2 - 0.8790 87.90%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.8515 85.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8349 83.49%
OATP1B3 inhibitior - 0.3152 31.52%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6526 65.26%
BSEP inhibitior + 0.7752 77.52%
P-glycoprotein inhibitior + 0.7615 76.15%
P-glycoprotein substrate + 0.5365 53.65%
CYP3A4 substrate + 0.7294 72.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8687 86.87%
CYP3A4 inhibition - 0.9072 90.72%
CYP2C9 inhibition - 0.8493 84.93%
CYP2C19 inhibition - 0.9348 93.48%
CYP2D6 inhibition - 0.9399 93.99%
CYP1A2 inhibition - 0.9005 90.05%
CYP2C8 inhibition + 0.6306 63.06%
CYP inhibitory promiscuity - 0.9315 93.15%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6163 61.63%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.9134 91.34%
Skin irritation + 0.5341 53.41%
Skin corrosion - 0.9434 94.34%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7575 75.75%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.6433 64.33%
skin sensitisation - 0.9069 90.69%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.8362 83.62%
Acute Oral Toxicity (c) III 0.6401 64.01%
Estrogen receptor binding + 0.7387 73.87%
Androgen receptor binding + 0.7450 74.50%
Thyroid receptor binding - 0.5829 58.29%
Glucocorticoid receptor binding + 0.6949 69.49%
Aromatase binding + 0.6766 67.66%
PPAR gamma + 0.7413 74.13%
Honey bee toxicity - 0.6661 66.61%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9583 95.83%

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 98.34% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.00% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.63% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 94.02% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.86% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.39% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 90.85% 94.75%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.69% 93.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.52% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.98% 95.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 88.48% 93.04%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.65% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.62% 89.00%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 86.25% 100.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 85.58% 96.21%
CHEMBL2996 Q05655 Protein kinase C delta 84.71% 97.79%
CHEMBL3401 O75469 Pregnane X receptor 83.78% 94.73%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.49% 97.36%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.63% 91.07%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.41% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.40% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.00% 100.00%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 81.90% 95.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.83% 97.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.37% 99.23%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.24% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.36% 95.89%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 80.15% 98.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10865639
LOTUS LTS0060833
wikiData Q104944634