Protopanaxatriol Oxide Ii

Details

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Internal ID baaec970-a22e-4f28-94e6-2fdd2731eac1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-17-[(2S,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,6,12-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H52O5/c1-25(2)21(33)10-12-27(5)20-15-18(31)23-17(30(8)14-11-22(35-30)26(3,4)34)9-13-28(23,6)29(20,7)16-19(32)24(25)27/h17-24,31-34H,9-16H2,1-8H3/t17-,18+,19-,20+,21-,22-,23-,24-,27+,28+,29+,30-/m0/s1
InChI Key XIGBHUXQOPWGDK-YDQYPMPQSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C30H52O5
Molecular Weight 492.70 g/mol
Exact Mass 492.38147475 g/mol
Topological Polar Surface Area (TPSA) 90.20 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.68
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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CHEMBL474277

2D Structure

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2D Structure of Protopanaxatriol Oxide Ii

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 - 0.6865 68.65%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7007 70.07%
OATP2B1 inhibitior - 0.5767 57.67%
OATP1B1 inhibitior + 0.8883 88.83%
OATP1B3 inhibitior + 0.9210 92.10%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7321 73.21%
BSEP inhibitior - 0.8095 80.95%
P-glycoprotein inhibitior - 0.6199 61.99%
P-glycoprotein substrate - 0.5988 59.88%
CYP3A4 substrate + 0.7221 72.21%
CYP2C9 substrate - 0.6036 60.36%
CYP2D6 substrate - 0.7058 70.58%
CYP3A4 inhibition - 0.7241 72.41%
CYP2C9 inhibition - 0.8642 86.42%
CYP2C19 inhibition - 0.8136 81.36%
CYP2D6 inhibition - 0.9530 95.30%
CYP1A2 inhibition - 0.7696 76.96%
CYP2C8 inhibition + 0.5207 52.07%
CYP inhibitory promiscuity - 0.8721 87.21%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5771 57.71%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9204 92.04%
Skin irritation - 0.5646 56.46%
Skin corrosion - 0.9145 91.45%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6682 66.82%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.8185 81.85%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.7858 78.58%
Acute Oral Toxicity (c) III 0.5401 54.01%
Estrogen receptor binding + 0.6827 68.27%
Androgen receptor binding + 0.7097 70.97%
Thyroid receptor binding + 0.6040 60.40%
Glucocorticoid receptor binding + 0.7462 74.62%
Aromatase binding + 0.7313 73.13%
PPAR gamma + 0.5336 53.36%
Honey bee toxicity - 0.6899 68.99%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9491 94.91%

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
CHEMBL1914 P06276 Butyrylcholinesterase 96.75% 95.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.95% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 94.62% 82.69%
CHEMBL218 P21554 Cannabinoid CB1 receptor 93.76% 96.61%
CHEMBL1871 P10275 Androgen Receptor 92.52% 96.43%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.15% 97.09%
CHEMBL4302 P08183 P-glycoprotein 1 91.26% 92.98%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 91.13% 89.05%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.57% 96.77%
CHEMBL259 P32245 Melanocortin receptor 4 90.25% 95.38%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 89.95% 95.58%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.67% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.42% 100.00%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 89.15% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 89.02% 97.79%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 87.55% 87.16%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.02% 85.30%
CHEMBL2179 P04062 Beta-glucocerebrosidase 86.51% 85.31%
CHEMBL4482 O96013 Serine/threonine-protein kinase PAK 4 86.34% 95.42%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.98% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.97% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.91% 95.89%
CHEMBL5600 P27448 Serine/threonine-protein kinase c-TAK1 84.51% 88.81%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.88% 95.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.74% 85.14%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 83.51% 97.31%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 82.79% 88.84%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.50% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.48% 96.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.27% 94.45%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.77% 97.14%
CHEMBL1974 P36888 Tyrosine-protein kinase receptor FLT3 81.00% 91.83%

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.
Panax vietnamensis

Cross-Links

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PubChem 15886257
LOTUS LTS0232733
wikiData Q105328461