XK-469 free acid, (R)-

Details

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Internal ID 85b93411-01c1-4f13-9f61-7f675e2bf0ca
Taxonomy Benzenoids > Benzene and substituted derivatives > 2-phenoxypropionic acids > Aryloxyphenoxypropionic acids
IUPAC Name (2R)-2-[4-(7-chloroquinoxalin-2-yl)oxyphenoxy]propanoic acid
SMILES (Canonical) CC(C(=O)O)OC1=CC=C(C=C1)OC2=CN=C3C=CC(=CC3=N2)Cl
SMILES (Isomeric) C[C@H](C(=O)O)OC1=CC=C(C=C1)OC2=CN=C3C=CC(=CC3=N2)Cl
InChI InChI=1S/C17H13ClN2O4/c1-10(17(21)22)23-12-3-5-13(6-4-12)24-16-9-19-14-7-2-11(18)8-15(14)20-16/h2-10H,1H3,(H,21,22)/t10-/m1/s1
InChI Key NUQZXROIVGBRGR-SNVBAGLBSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C17H13ClN2O4
Molecular Weight 344.70 g/mol
Exact Mass 344.0563846 g/mol
Topological Polar Surface Area (TPSA) 81.50 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.93
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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NSC-698215
UNII-8VSJ573G09
157542-91-1
8VSJ573G09
Propanoic acid, 2-(4-((7-chloro-2-quinoxalinyl)oxy)phenoxy)-, (2R)-
NSC698215
(R)-xk-469 free acid
Propanoic acid, (+)-(R)-
R(+)xk469
CHEMBL1741037
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of XK-469 free acid, (R)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9862 98.62%
Caco-2 + 0.5699 56.99%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.5822 58.22%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.9228 92.28%
OATP1B3 inhibitior + 0.9409 94.09%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8370 83.70%
P-glycoprotein inhibitior - 0.7290 72.90%
P-glycoprotein substrate - 0.8807 88.07%
CYP3A4 substrate + 0.5662 56.62%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.8670 86.70%
CYP3A4 inhibition - 0.8130 81.30%
CYP2C9 inhibition - 0.9287 92.87%
CYP2C19 inhibition - 0.8591 85.91%
CYP2D6 inhibition - 0.9604 96.04%
CYP1A2 inhibition + 0.6234 62.34%
CYP2C8 inhibition + 0.6265 62.65%
CYP inhibitory promiscuity - 0.7453 74.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7797 77.97%
Carcinogenicity (trinary) Non-required 0.5537 55.37%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9670 96.70%
Skin irritation - 0.7646 76.46%
Skin corrosion - 0.9634 96.34%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6846 68.46%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.7302 73.02%
skin sensitisation - 0.8737 87.37%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.7672 76.72%
Acute Oral Toxicity (c) III 0.6526 65.26%
Estrogen receptor binding + 0.6889 68.89%
Androgen receptor binding + 0.7760 77.60%
Thyroid receptor binding + 0.8320 83.20%
Glucocorticoid receptor binding + 0.8389 83.89%
Aromatase binding + 0.7925 79.25%
PPAR gamma + 0.8194 81.94%
Honey bee toxicity - 0.9595 95.95%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.8130 81.30%
Fish aquatic toxicity - 0.3643 36.43%

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
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.69% 99.15%
CHEMBL2243 O00519 Anandamide amidohydrolase 94.78% 97.53%
CHEMBL4208 P20618 Proteasome component C5 92.93% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.77% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.73% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.52% 96.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 91.43% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 90.68% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.24% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.17% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.22% 94.45%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 88.92% 92.29%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.44% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.26% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 85.87% 90.17%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.27% 100.00%
CHEMBL1907 P15144 Aminopeptidase N 84.88% 93.31%
CHEMBL3286 P00749 Urokinase-type plasminogen activator 84.57% 97.88%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.26% 85.30%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 84.20% 95.78%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.86% 97.36%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.76% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.52% 95.89%
CHEMBL1293289 P25440 Bromodomain-containing protein 2 81.36% 86.19%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.08% 90.24%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.84% 94.42%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.12% 90.71%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

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PubChem 3246729
NPASS NPC197141