kipukasin G

Details

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Internal ID 3cfd90c3-ff08-4dc3-a29e-b8fa6e1901ac
Taxonomy Nucleosides, nucleotides, and analogues > Pyrimidine nucleosides
IUPAC Name [(2R,3S,4R,5R)-4-hydroxy-2-(hydroxymethyl)-5-(3-methyl-2,4-dioxopyrimidin-1-yl)oxolan-3-yl] 4-hydroxy-2-methoxy-6-methylbenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H22N2O9/c1-9-6-10(23)7-11(28-3)14(9)18(26)30-16-12(8-22)29-17(15(16)25)21-5-4-13(24)20(2)19(21)27/h4-7,12,15-17,22-23,25H,8H2,1-3H3/t12-,15-,16-,17-/m1/s1
InChI Key CIJRLBYKDKLPQB-BASLNEPJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H22N2O9
Molecular Weight 422.40 g/mol
Exact Mass 422.13253028 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP -0.50
Atomic LogP (AlogP) -0.95
H-Bond Acceptor 11
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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NSC-787467
948574-03-6

2D Structure

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2D Structure of kipukasin G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7731 77.31%
Caco-2 - 0.7510 75.10%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.5705 57.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8755 87.55%
OATP1B3 inhibitior + 0.9309 93.09%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6718 67.18%
P-glycoprotein inhibitior - 0.4916 49.16%
P-glycoprotein substrate - 0.6540 65.40%
CYP3A4 substrate + 0.6483 64.83%
CYP2C9 substrate - 0.5975 59.75%
CYP2D6 substrate - 0.8648 86.48%
CYP3A4 inhibition - 0.7059 70.59%
CYP2C9 inhibition - 0.7550 75.50%
CYP2C19 inhibition - 0.8145 81.45%
CYP2D6 inhibition - 0.8944 89.44%
CYP1A2 inhibition - 0.9359 93.59%
CYP2C8 inhibition - 0.5666 56.66%
CYP inhibitory promiscuity - 0.6888 68.88%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.4926 49.26%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9457 94.57%
Skin irritation - 0.8352 83.52%
Skin corrosion - 0.9565 95.65%
Ames mutagenesis - 0.6732 67.32%
Human Ether-a-go-go-Related Gene inhibition + 0.6412 64.12%
Micronuclear + 0.9600 96.00%
Hepatotoxicity + 0.5389 53.89%
skin sensitisation - 0.9190 91.90%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7274 72.74%
Acute Oral Toxicity (c) III 0.6533 65.33%
Estrogen receptor binding + 0.6770 67.70%
Androgen receptor binding + 0.6696 66.96%
Thyroid receptor binding + 0.5281 52.81%
Glucocorticoid receptor binding + 0.6674 66.74%
Aromatase binding + 0.5822 58.22%
PPAR gamma + 0.6180 61.80%
Honey bee toxicity - 0.8213 82.13%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity - 0.4644 46.44%

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 98.18% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.12% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.45% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.71% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.58% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 91.48% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.74% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.44% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 89.34% 94.73%
CHEMBL4208 P20618 Proteasome component C5 88.21% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.50% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.58% 96.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.54% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.26% 99.17%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.66% 93.65%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 82.36% 90.93%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.15% 94.42%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.77% 91.07%

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 23624919
LOTUS LTS0087191
wikiData Q104959889