5-[(1S,3R,5S,6R,8R,9S,10R,13R,14R,16S,18R,20R,22S,24S,26S)-8,13,26-trihydroxy-1-methoxy-5,9,24-trimethyl-2,15,21,23-tetraoxaheptacyclo[20.3.1.03,20.05,18.06,14.09,13.014,16]hexacosan-10-yl]pyran-2-one

Details

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Internal ID 22457f5b-3143-4dbb-ae81-ee48451b32d4
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Bufanolides and derivatives
IUPAC Name 5-[(1S,3R,5S,6R,8R,9S,10R,13R,14R,16S,18R,20R,22S,24S,26S)-8,13,26-trihydroxy-1-methoxy-5,9,24-trimethyl-2,15,21,23-tetraoxaheptacyclo[20.3.1.03,20.05,18.06,14.09,13.014,16]hexacosan-10-yl]pyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H42O10/c1-15-12-29(36-4)25(34)26(38-15)39-19-9-17-10-23-31(41-23)21(27(17,2)13-20(19)40-29)11-22(32)28(3)18(7-8-30(28,31)35)16-5-6-24(33)37-14-16/h5-6,14-15,17-23,25-26,32,34-35H,7-13H2,1-4H3/t15-,17+,18+,19+,20+,21+,22+,23-,25-,26-,27-,28-,29-,30+,31+/m0/s1
InChI Key HYFHVAKYSKJTGB-RZCMQMJHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H42O10
Molecular Weight 574.70 g/mol
Exact Mass 574.27779753 g/mol
Topological Polar Surface Area (TPSA) 136.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 2.22
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-[(1S,3R,5S,6R,8R,9S,10R,13R,14R,16S,18R,20R,22S,24S,26S)-8,13,26-trihydroxy-1-methoxy-5,9,24-trimethyl-2,15,21,23-tetraoxaheptacyclo[20.3.1.03,20.05,18.06,14.09,13.014,16]hexacosan-10-yl]pyran-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9280 92.80%
Caco-2 - 0.8346 83.46%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6000 60.00%
OATP2B1 inhibitior - 0.7164 71.64%
OATP1B1 inhibitior + 0.8487 84.87%
OATP1B3 inhibitior + 0.8531 85.31%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9071 90.71%
BSEP inhibitior + 0.6984 69.84%
P-glycoprotein inhibitior + 0.6214 62.14%
P-glycoprotein substrate + 0.6350 63.50%
CYP3A4 substrate + 0.7205 72.05%
CYP2C9 substrate - 0.7987 79.87%
CYP2D6 substrate - 0.8502 85.02%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.7969 79.69%
CYP2C19 inhibition - 0.7991 79.91%
CYP2D6 inhibition - 0.9143 91.43%
CYP1A2 inhibition - 0.7659 76.59%
CYP2C8 inhibition + 0.5908 59.08%
CYP inhibitory promiscuity - 0.9183 91.83%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5869 58.69%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9403 94.03%
Skin irritation - 0.6714 67.14%
Skin corrosion - 0.9251 92.51%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3928 39.28%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5921 59.21%
skin sensitisation - 0.8836 88.36%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.7327 73.27%
Acute Oral Toxicity (c) II 0.4545 45.45%
Estrogen receptor binding + 0.7397 73.97%
Androgen receptor binding + 0.7369 73.69%
Thyroid receptor binding + 0.5563 55.63%
Glucocorticoid receptor binding + 0.6688 66.88%
Aromatase binding + 0.7487 74.87%
PPAR gamma + 0.7115 71.15%
Honey bee toxicity - 0.7408 74.08%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9559 95.59%

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 95.87% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.92% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.87% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.69% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.20% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 91.08% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.08% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.02% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.88% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.38% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.89% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.78% 94.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.88% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.53% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.21% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.00% 82.69%
CHEMBL4208 P20618 Proteasome component C5 83.65% 90.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.12% 97.28%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.03% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.45% 100.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.13% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.15% 96.77%

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.
Tylecodon grandiflorus

Cross-Links

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PubChem 163035876
LOTUS LTS0114168
wikiData Q105035281