Uralsaponin B

Details

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Internal ID 7b87d706-b45a-4ba1-a8c7-92fc675163b9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name 6-[2-carboxy-6-[(11-carboxy-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl)oxy]-3,5-dihydroxyoxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
SMILES (Canonical) CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)C)C(=O)C=C6C3(CCC7(C6CC(CC7)(C)C(=O)O)C)C)C)C
SMILES (Isomeric) CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)C)C(=O)C=C6C3(CCC7(C6CC(CC7)(C)C(=O)O)C)C)C)C
InChI InChI=1S/C42H62O16/c1-37(2)21-8-11-42(7)31(20(43)16-18-19-17-39(4,36(53)54)13-12-38(19,3)14-15-41(18,42)6)40(21,5)10-9-22(37)55-35-27(48)28(26(47)30(58-35)33(51)52)56-34-25(46)23(44)24(45)29(57-34)32(49)50/h16,19,21-31,34-35,44-48H,8-15,17H2,1-7H3,(H,49,50)(H,51,52)(H,53,54)
InChI Key KEIFOIQHFNUSQE-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C42H62O16
Molecular Weight 822.90 g/mol
Exact Mass 822.40378589 g/mol
Topological Polar Surface Area (TPSA) 267.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.25
H-Bond Acceptor 13
H-Bond Donor 8
Rotatable Bonds 7

Synonyms

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105038-43-5
6-[2-carboxy-6-[(11-carboxy-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl)oxy]-3,5-dihydroxyoxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
3 Hydroxy-11-oxoolean-12-en-30-oic acid-3-O-glucuronopyranosyl-(1-3)glucuronopyranoside
(3beta,20beta)-20-Carboxy-11-oxo-30-norolean-12-en-3-yl 3-O-beta-D-glucopyranuronosyl-beta-D-glucopyranosiduronic acid
29-hydroxy-11,29-dioxoolean-12-en-3-yl 3-o-hexopyranuronosylhexopyranosiduronic acid
DTXSID50909312
beta-D-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 3-O-beta-D-glucopyranuronosyl-

2D Structure

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2D Structure of Uralsaponin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8728 87.28%
Caco-2 - 0.8751 87.51%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8383 83.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.4804 48.04%
OATP1B3 inhibitior - 0.3963 39.63%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.6929 69.29%
BSEP inhibitior + 0.7234 72.34%
P-glycoprotein inhibitior + 0.7632 76.32%
P-glycoprotein substrate - 0.7786 77.86%
CYP3A4 substrate + 0.7172 71.72%
CYP2C9 substrate - 0.7908 79.08%
CYP2D6 substrate - 0.8981 89.81%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.8692 86.92%
CYP2C19 inhibition - 0.9112 91.12%
CYP2D6 inhibition - 0.9423 94.23%
CYP1A2 inhibition - 0.8358 83.58%
CYP2C8 inhibition + 0.6900 69.00%
CYP inhibitory promiscuity - 0.9568 95.68%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6106 61.06%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9084 90.84%
Skin irritation - 0.5295 52.95%
Skin corrosion - 0.9236 92.36%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4663 46.63%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.6533 65.33%
skin sensitisation - 0.8115 81.15%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) IV 0.6130 61.30%
Estrogen receptor binding + 0.7825 78.25%
Androgen receptor binding + 0.7341 73.41%
Thyroid receptor binding - 0.6663 66.63%
Glucocorticoid receptor binding + 0.7431 74.31%
Aromatase binding + 0.6730 67.30%
PPAR gamma + 0.7678 76.78%
Honey bee toxicity - 0.7226 72.26%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9886 98.86%

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
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 99.25% 94.78%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.15% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.01% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.61% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 90.05% 91.49%
CHEMBL221 P23219 Cyclooxygenase-1 89.52% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.41% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.07% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.23% 86.33%
CHEMBL2581 P07339 Cathepsin D 86.21% 98.95%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.50% 97.36%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.21% 99.23%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.67% 93.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.34% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.48% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.11% 92.94%
CHEMBL5255 O00206 Toll-like receptor 4 80.40% 92.50%

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.
Glycyrrhiza glabra
Glycyrrhiza inflata
Glycyrrhiza uralensis

Cross-Links

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PubChem 163744
NPASS NPC79958