b-Solamarine

Details

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Internal ID 508ad418-2178-45aa-8ef0-be51cbf479d2
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
IUPAC Name 2-[2-[4,5-dihydroxy-2-(hydroxymethyl)-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl)oxyoxan-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol
SMILES (Canonical) CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)OC9C(C(C(C(O9)C)O)O)O)O)O)C)C)C)NC1
SMILES (Isomeric) CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)OC9C(C(C(C(O9)C)O)O)O)O)O)C)C)C)NC1
InChI InChI=1S/C45H73NO15/c1-19-9-14-45(46-17-19)20(2)30-28(61-45)16-27-25-8-7-23-15-24(10-12-43(23,5)26(25)11-13-44(27,30)6)57-41-37(54)35(52)38(29(18-47)58-41)59-42-39(34(51)32(49)22(4)56-42)60-40-36(53)33(50)31(48)21(3)55-40/h7,19-22,24-42,46-54H,8-18H2,1-6H3
InChI Key VTYQXQQQKWLGBA-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C45H73NO15
Molecular Weight 868.10 g/mol
Exact Mass 867.49802062 g/mol
Topological Polar Surface Area (TPSA) 238.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.81
H-Bond Acceptor 16
H-Bond Donor 9
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of b-Solamarine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8227 82.27%
Caco-2 - 0.8840 88.40%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.5883 58.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9041 90.41%
OATP1B3 inhibitior + 0.9339 93.39%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8432 84.32%
P-glycoprotein inhibitior + 0.7273 72.73%
P-glycoprotein substrate + 0.5584 55.84%
CYP3A4 substrate + 0.7415 74.15%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.8216 82.16%
CYP3A4 inhibition - 0.9497 94.97%
CYP2C9 inhibition - 0.9216 92.16%
CYP2C19 inhibition - 0.9213 92.13%
CYP2D6 inhibition - 0.9346 93.46%
CYP1A2 inhibition - 0.9009 90.09%
CYP2C8 inhibition + 0.7262 72.62%
CYP inhibitory promiscuity - 0.8790 87.90%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4623 46.23%
Eye corrosion - 0.9862 98.62%
Eye irritation - 0.9131 91.31%
Skin irritation - 0.6850 68.50%
Skin corrosion - 0.9217 92.17%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8030 80.30%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.9500 95.00%
skin sensitisation - 0.8526 85.26%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.8761 87.61%
Acute Oral Toxicity (c) III 0.6991 69.91%
Estrogen receptor binding + 0.8582 85.82%
Androgen receptor binding + 0.6458 64.58%
Thyroid receptor binding - 0.5358 53.58%
Glucocorticoid receptor binding + 0.6093 60.93%
Aromatase binding + 0.6901 69.01%
PPAR gamma + 0.7613 76.13%
Honey bee toxicity - 0.6104 61.04%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.7285 72.85%

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 98.99% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.53% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.28% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 96.38% 95.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.72% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.48% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.30% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.71% 95.89%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 89.87% 89.05%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.82% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.16% 89.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.14% 96.61%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.01% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.52% 86.33%
CHEMBL1914 P06276 Butyrylcholinesterase 84.99% 95.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.37% 95.50%
CHEMBL2996 Q05655 Protein kinase C delta 83.10% 97.79%
CHEMBL2581 P07339 Cathepsin D 82.67% 98.95%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 82.27% 97.50%
CHEMBL332 P03956 Matrix metalloproteinase-1 81.95% 94.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.93% 92.94%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.98% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 80.64% 94.75%
CHEMBL5524 Q99873 Protein-arginine N-methyltransferase 1 80.63% 96.67%

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.
Solanum aviculare

Cross-Links

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PubChem 14428444
LOTUS LTS0242584
wikiData Q105293092