Shengjimycin B3

Details

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Internal ID 84c36108-769c-45e5-b189-8e660099de8c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Aminosaccharides > Aminoglycosides
IUPAC Name [(11Z,13Z)-6-[4-(dimethylamino)-3-hydroxy-5-(4-hydroxy-4,6-dimethyl-5-propanoyloxyoxan-2-yl)oxy-6-methyloxan-2-yl]oxy-10-[5-(dimethylamino)-6-methyloxan-2-yl]oxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-4-yl] propanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C49H82N2O16/c1-14-37(53)63-36-26-39(55)59-29(4)19-17-16-18-20-35(64-40-22-21-34(50(9)10)30(5)60-40)28(3)25-33(23-24-52)45(46(36)58-13)67-48-43(56)42(51(11)12)44(31(6)62-48)66-41-27-49(8,57)47(32(7)61-41)65-38(54)15-2/h16-18,20,24,28-36,40-48,56-57H,14-15,19,21-23,25-27H2,1-13H3/b17-16-,20-18-
InChI Key NGDGWCBJRIMBLF-OTMJARGSSA-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 4.20
Atomic LogP (AlogP) 4.25
H-Bond Acceptor 18
H-Bond Donor 2
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Shengjimycin B3

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7347 73.47%
Caco-2 - 0.8595 85.95%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.9714 97.14%
Subcellular localzation Mitochondria 0.5406 54.06%
OATP2B1 inhibitior - 0.8649 86.49%
OATP1B1 inhibitior + 0.8840 88.40%
OATP1B3 inhibitior + 0.9377 93.77%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9869 98.69%
P-glycoprotein inhibitior + 0.7650 76.50%
P-glycoprotein substrate + 0.8273 82.73%
CYP3A4 substrate + 0.6587 65.87%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8853 88.53%
CYP3A4 inhibition - 0.7614 76.14%
CYP2C9 inhibition - 0.9029 90.29%
CYP2C19 inhibition - 0.8791 87.91%
CYP2D6 inhibition - 0.9082 90.82%
CYP1A2 inhibition - 0.9230 92.30%
CYP2C8 inhibition + 0.7222 72.22%
CYP inhibitory promiscuity - 0.9623 96.23%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5481 54.81%
Eye corrosion - 0.9858 98.58%
Eye irritation - 0.9065 90.65%
Skin irritation - 0.7556 75.56%
Skin corrosion - 0.9091 90.91%
Ames mutagenesis - 0.6670 66.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8082 80.82%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.6785 67.85%
skin sensitisation - 0.8680 86.80%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6965 69.65%
Acute Oral Toxicity (c) III 0.6098 60.98%
Estrogen receptor binding + 0.5314 53.14%
Androgen receptor binding + 0.6815 68.15%
Thyroid receptor binding + 0.5749 57.49%
Glucocorticoid receptor binding + 0.6939 69.39%
Aromatase binding - 0.6424 64.24%
PPAR gamma + 0.8039 80.39%
Honey bee toxicity - 0.5277 52.77%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.7134 71.34%

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 98.82% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.21% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.11% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.22% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.29% 89.00%
CHEMBL340 P08684 Cytochrome P450 3A4 91.68% 91.19%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.30% 99.17%
CHEMBL1974 P36888 Tyrosine-protein kinase receptor FLT3 90.53% 91.83%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.41% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.21% 92.94%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.19% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.18% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.79% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.04% 95.89%
CHEMBL3922 P50579 Methionine aminopeptidase 2 84.98% 97.28%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.44% 94.33%
CHEMBL2664 P23526 Adenosylhomocysteinase 84.22% 86.67%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.90% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.05% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.84% 100.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 82.42% 97.33%
CHEMBL4208 P20618 Proteasome component C5 81.72% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.70% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.08% 92.62%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.05% 91.24%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.01% 97.36%
CHEMBL5255 O00206 Toll-like receptor 4 80.71% 92.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.43% 97.14%

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.
There are no matching plants.

Cross-Links

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PubChem 139586100
LOTUS LTS0114161
wikiData Q77498866