(3beta,6alpha,16beta,20R,24S)-20,24-Epoxylanost-9(11)-ene-3,6,16,25-tetrol

Details

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Internal ID 00cf4cc4-18c4-4367-9afc-a482528143e6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (3S,5R,6S,8S,10S,13R,14S,16S,17R)-17-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,6,16-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H50O5/c1-25(2)21(33)10-12-27(5)17-9-13-28(6)24(30(8)14-11-22(35-30)26(3,4)34)20(32)16-29(28,7)18(17)15-19(31)23(25)27/h9,18-24,31-34H,10-16H2,1-8H3/t18-,19+,20+,21+,22+,23+,24+,27-,28-,29+,30-/m1/s1
InChI Key KNESISUQBYQIIU-LOIFQKOGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O5
Molecular Weight 490.70 g/mol
Exact Mass 490.36582469 g/mol
Topological Polar Surface Area (TPSA) 90.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.60
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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86541-79-9
DTXSID401170200
HY-N7924
MS-29123
CS-0138811
(3beta,6alpha,16beta,20R,24S)-20,24-Epoxylanost-9(11)-ene-3,6,16,25-tetrol

2D Structure

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2D Structure of (3beta,6alpha,16beta,20R,24S)-20,24-Epoxylanost-9(11)-ene-3,6,16,25-tetrol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 - 0.6076 60.76%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7051 70.51%
OATP2B1 inhibitior - 0.7174 71.74%
OATP1B1 inhibitior + 0.8929 89.29%
OATP1B3 inhibitior + 0.9543 95.43%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6885 68.85%
BSEP inhibitior - 0.5891 58.91%
P-glycoprotein inhibitior - 0.6072 60.72%
P-glycoprotein substrate - 0.5941 59.41%
CYP3A4 substrate + 0.6823 68.23%
CYP2C9 substrate - 0.7722 77.22%
CYP2D6 substrate - 0.7344 73.44%
CYP3A4 inhibition - 0.7521 75.21%
CYP2C9 inhibition - 0.8294 82.94%
CYP2C19 inhibition - 0.7837 78.37%
CYP2D6 inhibition - 0.9383 93.83%
CYP1A2 inhibition - 0.7663 76.63%
CYP2C8 inhibition + 0.5305 53.05%
CYP inhibitory promiscuity - 0.7495 74.95%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4595 45.95%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9412 94.12%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9292 92.92%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4409 44.09%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8046 80.46%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.8274 82.74%
Acute Oral Toxicity (c) I 0.6419 64.19%
Estrogen receptor binding + 0.7495 74.95%
Androgen receptor binding + 0.7411 74.11%
Thyroid receptor binding + 0.6483 64.83%
Glucocorticoid receptor binding + 0.7907 79.07%
Aromatase binding + 0.7100 71.00%
PPAR gamma + 0.5734 57.34%
Honey bee toxicity - 0.8191 81.91%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9836 98.36%

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 97.15% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.19% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.55% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.99% 97.25%
CHEMBL2996 Q05655 Protein kinase C delta 90.59% 97.79%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 89.47% 89.05%
CHEMBL1871 P10275 Androgen Receptor 88.40% 96.43%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.57% 96.61%
CHEMBL259 P32245 Melanocortin receptor 4 87.25% 95.38%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.82% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.73% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.35% 96.77%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.00% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.50% 95.89%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.94% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 81.53% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.05% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.33% 92.94%

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.
Astragalus trimestris

Cross-Links

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PubChem 11944583
LOTUS LTS0263862
wikiData Q104246816