Shengjimycin B2beta

Details

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Internal ID ce8d9d3e-79ab-46f6-8ee4-83a046eca442
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Aminosaccharides > Aminoglycosides
IUPAC Name [6-[6-[[(11Z,13Z)-4-acetyloxy-10-[5-(dimethylamino)-6-methyloxan-2-yl]oxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-6-yl]oxy]-4-(dimethylamino)-5-hydroxy-2-methyloxan-3-yl]oxy-4-hydroxy-2,4-dimethyloxan-3-yl] 2-methylpropanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C49H82N2O16/c1-27(2)47(56)67-46-32(7)61-40(26-49(46,9)57)65-43-31(6)62-48(42(55)41(43)51(12)13)66-44-34(22-23-52)24-28(3)36(64-39-21-20-35(50(10)11)30(5)60-39)19-17-15-16-18-29(4)59-38(54)25-37(45(44)58-14)63-33(8)53/h15-17,19,23,27-32,34-37,39-46,48,55,57H,18,20-22,24-26H2,1-14H3/b16-15-,19-17-
InChI Key KULCFBWWBNGLHQ-RKXLPSGMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C49H82N2O16
Molecular Weight 955.20 g/mol
Exact Mass 954.56643453 g/mol
Topological Polar Surface Area (TPSA) 208.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.10
H-Bond Acceptor 18
H-Bond Donor 2
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Shengjimycin B2beta

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5787 57.87%
Caco-2 - 0.8609 86.09%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.9286 92.86%
Subcellular localzation Mitochondria 0.5998 59.98%
OATP2B1 inhibitior - 0.7302 73.02%
OATP1B1 inhibitior + 0.8768 87.68%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9828 98.28%
P-glycoprotein inhibitior + 0.7661 76.61%
P-glycoprotein substrate + 0.8261 82.61%
CYP3A4 substrate + 0.6693 66.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8853 88.53%
CYP3A4 inhibition - 0.8505 85.05%
CYP2C9 inhibition - 0.9107 91.07%
CYP2C19 inhibition - 0.8950 89.50%
CYP2D6 inhibition - 0.9162 91.62%
CYP1A2 inhibition - 0.9281 92.81%
CYP2C8 inhibition + 0.7211 72.11%
CYP inhibitory promiscuity - 0.9753 97.53%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5376 53.76%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.9061 90.61%
Skin irritation - 0.7522 75.22%
Skin corrosion - 0.9106 91.06%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7705 77.05%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.7086 70.86%
skin sensitisation - 0.8675 86.75%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6973 69.73%
Acute Oral Toxicity (c) III 0.4689 46.89%
Estrogen receptor binding - 0.5365 53.65%
Androgen receptor binding + 0.6905 69.05%
Thyroid receptor binding + 0.5579 55.79%
Glucocorticoid receptor binding + 0.7001 70.01%
Aromatase binding - 0.6929 69.29%
PPAR gamma + 0.8053 80.53%
Honey bee toxicity - 0.5256 52.56%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity - 0.3616 36.16%

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 99.58% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.38% 96.09%
CHEMBL2581 P07339 Cathepsin D 98.07% 98.95%
CHEMBL204 P00734 Thrombin 95.32% 96.01%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.80% 97.25%
CHEMBL340 P08684 Cytochrome P450 3A4 94.60% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.17% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 92.90% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.70% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.59% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.61% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.45% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.42% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.52% 92.62%
CHEMBL3922 P50579 Methionine aminopeptidase 2 86.81% 97.28%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.79% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.72% 96.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.93% 91.07%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.30% 94.33%
CHEMBL4015 P41597 C-C chemokine receptor type 2 83.63% 98.57%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.55% 97.36%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.47% 93.56%
CHEMBL1974 P36888 Tyrosine-protein kinase receptor FLT3 83.26% 91.83%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.98% 91.24%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.85% 97.14%
CHEMBL3891 P07384 Calpain 1 80.78% 93.04%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.30% 92.94%

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 139588164
LOTUS LTS0233192
wikiData Q105146208