7-O-(alpha-glucosyl)-5,6-dihydrocineromycin B

Details

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Internal ID 61f280e5-6fad-4f5d-85e1-ce8e64d50a68
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (3E,5R,8S,9E,13S,14R)-5-hydroxy-5,9,13,14-tetramethyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-oxacyclotetradeca-3,9-dien-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H38O9/c1-13-6-5-7-14(2)16(8-10-23(4,29)11-9-18(25)30-15(13)3)31-22-21(28)20(27)19(26)17(12-24)32-22/h7,9,11,13,15-17,19-22,24,26-29H,5-6,8,10,12H2,1-4H3/b11-9+,14-7+/t13-,15+,16-,17+,19+,20-,21+,22-,23+/m0/s1
InChI Key ZXQPHIUZDVZILF-KCFREIJWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H38O9
Molecular Weight 458.50 g/mol
Exact Mass 458.25158279 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.57
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-O-(alpha-glucosyl)-5,6-dihydrocineromycin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6674 66.74%
Caco-2 - 0.7471 74.71%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.8122 81.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8703 87.03%
OATP1B3 inhibitior + 0.8059 80.59%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7026 70.26%
BSEP inhibitior - 0.7671 76.71%
P-glycoprotein inhibitior - 0.7135 71.35%
P-glycoprotein substrate - 0.7576 75.76%
CYP3A4 substrate + 0.6598 65.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8960 89.60%
CYP3A4 inhibition - 0.9233 92.33%
CYP2C9 inhibition - 0.8698 86.98%
CYP2C19 inhibition - 0.9012 90.12%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.8502 85.02%
CYP2C8 inhibition - 0.6084 60.84%
CYP inhibitory promiscuity - 0.9549 95.49%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6999 69.99%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9740 97.40%
Skin irritation - 0.6118 61.18%
Skin corrosion - 0.9508 95.08%
Ames mutagenesis - 0.6795 67.95%
Human Ether-a-go-go-Related Gene inhibition - 0.3727 37.27%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.6101 61.01%
skin sensitisation - 0.8727 87.27%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6355 63.55%
Acute Oral Toxicity (c) III 0.5991 59.91%
Estrogen receptor binding + 0.6663 66.63%
Androgen receptor binding - 0.6029 60.29%
Thyroid receptor binding - 0.6127 61.27%
Glucocorticoid receptor binding + 0.5675 56.75%
Aromatase binding - 0.5508 55.08%
PPAR gamma - 0.4831 48.31%
Honey bee toxicity - 0.8100 81.00%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6150 61.50%
Fish aquatic toxicity + 0.7276 72.76%

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 96.46% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.97% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.95% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.74% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.73% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.31% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.05% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.91% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.33% 96.09%
CHEMBL4072 P07858 Cathepsin B 87.05% 93.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.79% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.65% 89.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 85.55% 91.24%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.83% 96.21%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 83.10% 95.83%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.55% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.59% 99.23%
CHEMBL5255 O00206 Toll-like receptor 4 81.36% 92.50%
CHEMBL3401 O75469 Pregnane X receptor 80.14% 94.73%

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 10837579
LOTUS LTS0004600
wikiData Q75062233