(5R,8R,9R,10S,11R,13R,14R,17S)-11-hydroxy-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

Details

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Internal ID f75fe571-0739-464a-812a-67ceb2c327d3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (5R,8R,9R,10S,11R,13R,14R,17S)-11-hydroxy-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H50O4/c1-25(2)21-10-15-29(7)24(27(21,5)13-11-22(25)32)20(31)17-19-18(9-14-28(19,29)6)30(8)16-12-23(34-30)26(3,4)33/h18-21,23-24,31,33H,9-17H2,1-8H3/t18-,19+,20+,21-,23+,24+,27-,28+,29+,30-/m0/s1
InChI Key DBMMBHFXIAXXLI-KPVQNITCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O4
Molecular Weight 474.70 g/mol
Exact Mass 474.37091007 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.92
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5R,8R,9R,10S,11R,13R,14R,17S)-11-hydroxy-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 - 0.5956 59.56%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7971 79.71%
OATP2B1 inhibitior - 0.5730 57.30%
OATP1B1 inhibitior + 0.8465 84.65%
OATP1B3 inhibitior + 0.9316 93.16%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6358 63.58%
BSEP inhibitior + 0.5874 58.74%
P-glycoprotein inhibitior - 0.6263 62.63%
P-glycoprotein substrate - 0.7264 72.64%
CYP3A4 substrate + 0.7100 71.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7804 78.04%
CYP3A4 inhibition - 0.6019 60.19%
CYP2C9 inhibition - 0.8364 83.64%
CYP2C19 inhibition - 0.8167 81.67%
CYP2D6 inhibition - 0.9540 95.40%
CYP1A2 inhibition - 0.7752 77.52%
CYP2C8 inhibition - 0.5661 56.61%
CYP inhibitory promiscuity - 0.9121 91.21%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6030 60.30%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9275 92.75%
Skin irritation + 0.4894 48.94%
Skin corrosion - 0.9098 90.98%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4137 41.37%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.6967 69.67%
skin sensitisation - 0.8224 82.24%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.6697 66.97%
Acute Oral Toxicity (c) III 0.5397 53.97%
Estrogen receptor binding + 0.7601 76.01%
Androgen receptor binding + 0.7151 71.51%
Thyroid receptor binding + 0.6068 60.68%
Glucocorticoid receptor binding + 0.7974 79.74%
Aromatase binding + 0.7246 72.46%
PPAR gamma + 0.5455 54.55%
Honey bee toxicity - 0.7808 78.08%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9631 96.31%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.53% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.42% 91.11%
CHEMBL1914 P06276 Butyrylcholinesterase 91.70% 95.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.39% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.62% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.58% 82.69%
CHEMBL230 P35354 Cyclooxygenase-2 89.38% 89.63%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.88% 99.23%
CHEMBL1871 P10275 Androgen Receptor 88.73% 96.43%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.14% 85.14%
CHEMBL259 P32245 Melanocortin receptor 4 87.86% 95.38%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.78% 93.04%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.74% 96.09%
CHEMBL204 P00734 Thrombin 86.64% 96.01%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.81% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.66% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.83% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.45% 86.33%
CHEMBL1902 P62942 FK506-binding protein 1A 82.91% 97.05%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 81.51% 97.33%
CHEMBL4302 P08183 P-glycoprotein 1 81.19% 92.98%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.33% 89.00%

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.
Veronica cupressoides

Cross-Links

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PubChem 14587779
LOTUS LTS0228699
wikiData Q104974590