3-(N-succinyl argininyl)bufotalin

Details

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Internal ID 14bdce59-f93f-4c62-9255-d1cf0e762346
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Bufanolides and derivatives
IUPAC Name (2S)-2-[[4-[[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-16-acetyloxy-14-hydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]-4-oxobutanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H52N4O10/c1-20(41)49-27-18-36(47)25-8-7-22-17-23(50-30(44)11-9-28(42)40-26(32(45)46)5-4-16-39-33(37)38)12-14-34(22,2)24(25)13-15-35(36,3)31(27)21-6-10-29(43)48-19-21/h6,10,19,22-27,31,47H,4-5,7-9,11-18H2,1-3H3,(H,40,42)(H,45,46)(H4,37,38,39)/t22-,23+,24+,25-,26+,27+,31+,34+,35-,36+/m1/s1
InChI Key ZHIFTHYTXVBJCZ-FJRGKVFBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H52N4O10
Molecular Weight 700.80 g/mol
Exact Mass 700.36834387 g/mol
Topological Polar Surface Area (TPSA) 230.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 2.74
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(N-succinyl argininyl)bufotalin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8621 86.21%
Caco-2 - 0.8595 85.95%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6908 69.08%
OATP2B1 inhibitior - 0.5684 56.84%
OATP1B1 inhibitior + 0.8203 82.03%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.7846 78.46%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8577 85.77%
P-glycoprotein inhibitior + 0.7508 75.08%
P-glycoprotein substrate + 0.6862 68.62%
CYP3A4 substrate + 0.7545 75.45%
CYP2C9 substrate - 0.5958 59.58%
CYP2D6 substrate - 0.8673 86.73%
CYP3A4 inhibition - 0.8473 84.73%
CYP2C9 inhibition - 0.7687 76.87%
CYP2C19 inhibition - 0.7052 70.52%
CYP2D6 inhibition - 0.8553 85.53%
CYP1A2 inhibition - 0.7901 79.01%
CYP2C8 inhibition + 0.6970 69.70%
CYP inhibitory promiscuity - 0.9028 90.28%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6060 60.60%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.9143 91.43%
Skin irritation - 0.7641 76.41%
Skin corrosion - 0.9257 92.57%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5528 55.28%
Micronuclear + 0.6800 68.00%
Hepatotoxicity - 0.6523 65.23%
skin sensitisation - 0.8437 84.37%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.6278 62.78%
Acute Oral Toxicity (c) III 0.5349 53.49%
Estrogen receptor binding + 0.8322 83.22%
Androgen receptor binding + 0.7588 75.88%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6774 67.74%
Aromatase binding + 0.6856 68.56%
PPAR gamma + 0.7287 72.87%
Honey bee toxicity - 0.6988 69.88%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9496 94.96%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.62% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.54% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.24% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.80% 97.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 96.64% 96.38%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.88% 99.17%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 94.35% 82.69%
CHEMBL2581 P07339 Cathepsin D 93.77% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.57% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.47% 86.33%
CHEMBL2492 P36544 Neuronal acetylcholine receptor protein alpha-7 subunit 89.08% 88.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.37% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 88.01% 91.19%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.88% 96.00%
CHEMBL5028 O14672 ADAM10 86.63% 97.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.51% 95.89%
CHEMBL2514 O95665 Neurotensin receptor 2 85.38% 100.00%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 84.92% 96.25%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.89% 90.71%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.25% 94.62%
CHEMBL4578 Q14680 Maternal embryonic leucine zipper kinase 83.02% 81.58%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.50% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.02% 93.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.96% 95.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.86% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.42% 99.23%
CHEMBL204 P00734 Thrombin 80.19% 96.01%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.13% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162925488
LOTUS LTS0243719
wikiData Q105375758