(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1R,2S,6R,9S,11R,14S,15S,17R,18S,20S,23R,24S)-17-hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-20-yl]oxy]oxane-3,4,5-triol

Details

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Internal ID 941c0f00-6d9e-4762-834c-79886116a1d8
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
IUPAC Name (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1R,2S,6R,9S,11R,14S,15S,17R,18S,20S,23R,24S)-17-hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-20-yl]oxy]oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H55NO7/c1-16-4-7-26-17(2)19-5-6-20-21(23(19)14-34(26)13-16)11-24-22(20)12-27(36)25-10-18(8-9-33(24,25)3)40-32-31(39)30(38)29(37)28(15-35)41-32/h16-32,35-39H,4-15H2,1-3H3/t16-,17?,18+,19+,20-,21-,22+,23-,24+,25-,26+,27-,28-,29-,30+,31-,32-,33-/m1/s1
InChI Key RRZZOQYXEGRKNH-FRKSFXGZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C33H55NO7
Molecular Weight 577.80 g/mol
Exact Mass 577.39785309 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 2.39
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1R,2S,6R,9S,11R,14S,15S,17R,18S,20S,23R,24S)-17-hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-20-yl]oxy]oxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5613 56.13%
Caco-2 - 0.8439 84.39%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Lysosomes 0.7558 75.58%
OATP2B1 inhibitior - 0.5804 58.04%
OATP1B1 inhibitior + 0.8894 88.94%
OATP1B3 inhibitior + 0.9362 93.62%
MATE1 inhibitior - 0.9412 94.12%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8414 84.14%
P-glycoprotein inhibitior - 0.4936 49.36%
P-glycoprotein substrate - 0.5832 58.32%
CYP3A4 substrate + 0.7266 72.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7424 74.24%
CYP3A4 inhibition - 0.8752 87.52%
CYP2C9 inhibition - 0.9172 91.72%
CYP2C19 inhibition - 0.9091 90.91%
CYP2D6 inhibition - 0.9368 93.68%
CYP1A2 inhibition - 0.9532 95.32%
CYP2C8 inhibition - 0.5903 59.03%
CYP inhibitory promiscuity - 0.9818 98.18%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5638 56.38%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.9183 91.83%
Skin irritation - 0.7580 75.80%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.8534 85.34%
Human Ether-a-go-go-Related Gene inhibition - 0.3725 37.25%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.7174 71.74%
skin sensitisation - 0.8797 87.97%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6666 66.66%
Acute Oral Toxicity (c) III 0.4365 43.65%
Estrogen receptor binding + 0.5551 55.51%
Androgen receptor binding + 0.6902 69.02%
Thyroid receptor binding - 0.6085 60.85%
Glucocorticoid receptor binding - 0.5691 56.91%
Aromatase binding + 0.5826 58.26%
PPAR gamma + 0.5255 52.55%
Honey bee toxicity - 0.7312 73.12%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.6794 67.94%

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 98.44% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.24% 96.09%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 97.28% 89.05%
CHEMBL218 P21554 Cannabinoid CB1 receptor 93.30% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.86% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.78% 91.11%
CHEMBL237 P41145 Kappa opioid receptor 92.41% 98.10%
CHEMBL206 P03372 Estrogen receptor alpha 92.34% 97.64%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.54% 92.86%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.40% 96.21%
CHEMBL233 P35372 Mu opioid receptor 88.28% 97.93%
CHEMBL226 P30542 Adenosine A1 receptor 87.82% 95.93%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.52% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.75% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 86.16% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.54% 89.00%
CHEMBL2534 O15530 3-phosphoinositide dependent protein kinase-1 84.24% 95.36%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 84.18% 98.46%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.46% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.15% 94.45%
CHEMBL344 Q99705 Melanin-concentrating hormone receptor 1 83.04% 92.50%
CHEMBL238 Q01959 Dopamine transporter 81.79% 95.88%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.55% 95.89%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.95% 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.
Fritillaria persica

Cross-Links

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PubChem 101635477
LOTUS LTS0151837
wikiData Q105244493