Goyaprosaponin

Details

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Internal ID bd6ad796-a7a1-4ee4-84e7-2df2bcc99fb0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-carboxy-4-formyl-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H64O15/c1-37(2)13-15-42(36(52)53)16-14-40(5)20(21(42)17-37)7-8-24-38(3)11-10-25(39(4,19-44)23(38)9-12-41(24,40)6)55-35-32(29(48)28(47)31(56-35)33(50)51)57-34-30(49)27(46)26(45)22(18-43)54-34/h7,19,21-32,34-35,43,45-49H,8-18H2,1-6H3,(H,50,51)(H,52,53)/t21-,22+,23+,24+,25-,26-,27-,28-,29-,30+,31-,32+,34-,35+,38-,39-,40+,41+,42-/m0/s1
InChI Key GBNOIXDJNQHMIV-CHTALKLSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C42H64O15
Molecular Weight 808.90 g/mol
Exact Mass 808.42452133 g/mol
Topological Polar Surface Area (TPSA) 250.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.15
H-Bond Acceptor 13
H-Bond Donor 8
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Goyaprosaponin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7941 79.41%
Caco-2 - 0.8849 88.49%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.8948 89.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7630 76.30%
OATP1B3 inhibitior - 0.5056 50.56%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.6474 64.74%
BSEP inhibitior + 0.5559 55.59%
P-glycoprotein inhibitior + 0.7583 75.83%
P-glycoprotein substrate - 0.7969 79.69%
CYP3A4 substrate + 0.7103 71.03%
CYP2C9 substrate - 0.8127 81.27%
CYP2D6 substrate - 0.8768 87.68%
CYP3A4 inhibition - 0.8459 84.59%
CYP2C9 inhibition - 0.8380 83.80%
CYP2C19 inhibition - 0.9220 92.20%
CYP2D6 inhibition - 0.9493 94.93%
CYP1A2 inhibition - 0.8499 84.99%
CYP2C8 inhibition + 0.7096 70.96%
CYP inhibitory promiscuity - 0.9381 93.81%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6298 62.98%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9099 90.99%
Skin irritation - 0.5723 57.23%
Skin corrosion - 0.9450 94.50%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6472 64.72%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.8875 88.75%
skin sensitisation - 0.9064 90.64%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.7728 77.28%
Acute Oral Toxicity (c) III 0.7628 76.28%
Estrogen receptor binding + 0.7732 77.32%
Androgen receptor binding + 0.7386 73.86%
Thyroid receptor binding - 0.6288 62.88%
Glucocorticoid receptor binding + 0.6826 68.26%
Aromatase binding + 0.6162 61.62%
PPAR gamma + 0.7575 75.75%
Honey bee toxicity - 0.7262 72.62%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6555 65.55%
Fish aquatic toxicity + 0.9778 97.78%

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 95.55% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.28% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.32% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.68% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.63% 97.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.45% 97.36%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.71% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.69% 86.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.50% 93.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.28% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.15% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.99% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.46% 100.00%
CHEMBL2581 P07339 Cathepsin D 82.26% 98.95%
CHEMBL5255 O00206 Toll-like receptor 4 81.76% 92.50%
CHEMBL5028 O14672 ADAM10 80.64% 97.50%

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.
Psammosilene tunicoides

Cross-Links

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PubChem 10581231
NPASS NPC212940