(1R,2S,5S,6R,9R,12S,13S,16S,18S)-16-[(2R,4R,5S,6S)-5-amino-4-methoxy-6-methyloxan-2-yl]oxy-6,13-dimethyl-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icosane-2,6-diol

Details

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Internal ID 6135fe90-7021-403d-9e62-f1311a9d5b63
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides
IUPAC Name (1R,2S,5S,6R,9R,12S,13S,16S,18S)-16-[(2R,4R,5S,6S)-5-amino-4-methoxy-6-methyloxan-2-yl]oxy-6,13-dimethyl-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icosane-2,6-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H47NO6/c1-16-24(29)21(32-4)14-23(34-16)35-18-7-10-25(2)17(13-18)5-6-20-19(25)8-11-27-15-33-26(3,30)22(27)9-12-28(20,27)31/h16-24,30-31H,5-15,29H2,1-4H3/t16-,17-,18-,19-,20+,21+,22+,23-,24-,25-,26+,27-,28-/m0/s1
InChI Key XPLAXRSHXHPUNS-AJXXJKKOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H47NO6
Molecular Weight 493.70 g/mol
Exact Mass 493.34033822 g/mol
Topological Polar Surface Area (TPSA) 103.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.34
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2S,5S,6R,9R,12S,13S,16S,18S)-16-[(2R,4R,5S,6S)-5-amino-4-methoxy-6-methyloxan-2-yl]oxy-6,13-dimethyl-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icosane-2,6-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7882 78.82%
Caco-2 - 0.7604 76.04%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.5141 51.41%
OATP2B1 inhibitior - 0.5727 57.27%
OATP1B1 inhibitior + 0.8842 88.42%
OATP1B3 inhibitior + 0.9150 91.50%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5461 54.61%
P-glycoprotein inhibitior - 0.5153 51.53%
P-glycoprotein substrate + 0.6220 62.20%
CYP3A4 substrate + 0.7225 72.25%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.7679 76.79%
CYP3A4 inhibition - 0.9259 92.59%
CYP2C9 inhibition - 0.8969 89.69%
CYP2C19 inhibition - 0.8747 87.47%
CYP2D6 inhibition - 0.9265 92.65%
CYP1A2 inhibition - 0.8900 89.00%
CYP2C8 inhibition - 0.5804 58.04%
CYP inhibitory promiscuity - 0.8978 89.78%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5519 55.19%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.9417 94.17%
Skin irritation - 0.7470 74.70%
Skin corrosion - 0.9223 92.23%
Ames mutagenesis - 0.6354 63.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4243 42.43%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.6813 68.13%
skin sensitisation - 0.8712 87.12%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6090 60.90%
Acute Oral Toxicity (c) III 0.4526 45.26%
Estrogen receptor binding + 0.6833 68.33%
Androgen receptor binding + 0.7425 74.25%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6991 69.91%
Aromatase binding + 0.5853 58.53%
PPAR gamma + 0.5390 53.90%
Honey bee toxicity - 0.5956 59.56%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.3738 37.38%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.48% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.33% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.00% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 96.63% 92.94%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.07% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 93.01% 100.00%
CHEMBL2243 O00519 Anandamide amidohydrolase 91.37% 97.53%
CHEMBL1871 P10275 Androgen Receptor 89.81% 96.43%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 89.40% 97.31%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.60% 96.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.05% 95.89%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.74% 82.69%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 83.89% 95.58%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 83.87% 98.99%
CHEMBL204 P00734 Thrombin 83.73% 96.01%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.64% 97.14%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 83.49% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.17% 86.33%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 83.06% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.54% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.47% 97.25%
CHEMBL1914 P06276 Butyrylcholinesterase 81.85% 95.00%
CHEMBL284 P27487 Dipeptidyl peptidase IV 81.20% 95.69%

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.
Holarrhena pubescens

Cross-Links

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PubChem 101306836
NPASS NPC95639