Tetraacetyl-d-xylonic nitrile

Details

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Internal ID 31be0362-1259-4a56-bdcc-cf9cf277d624
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tetracarboxylic acids and derivatives
IUPAC Name (2,3,4-triacetyloxy-5-cyano-5-oxopentyl) acetate
SMILES (Canonical) CC(=O)OCC(C(C(C(=O)C#N)OC(=O)C)OC(=O)C)OC(=O)C
SMILES (Isomeric) CC(=O)OCC(C(C(C(=O)C#N)OC(=O)C)OC(=O)C)OC(=O)C
InChI InChI=1S/C14H17NO9/c1-7(16)21-6-12(22-8(2)17)14(24-10(4)19)13(11(20)5-15)23-9(3)18/h12-14H,6H2,1-4H3
InChI Key UJBBVYYPLDKALG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H17NO9
Molecular Weight 343.29 g/mol
Exact Mass 343.09033112 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP -0.40
Atomic LogP (AlogP) -0.56
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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UJBBVYYPLDKALG-UHFFFAOYSA-N

2D Structure

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2D Structure of Tetraacetyl-d-xylonic nitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9278 92.78%
Caco-2 - 0.6124 61.24%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8497 84.97%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.9552 95.52%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7058 70.58%
P-glycoprotein inhibitior - 0.5670 56.70%
P-glycoprotein substrate - 0.8754 87.54%
CYP3A4 substrate - 0.5084 50.84%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.8730 87.30%
CYP3A4 inhibition - 0.6977 69.77%
CYP2C9 inhibition - 0.8403 84.03%
CYP2C19 inhibition - 0.8666 86.66%
CYP2D6 inhibition - 0.9117 91.17%
CYP1A2 inhibition - 0.8304 83.04%
CYP2C8 inhibition - 0.9096 90.96%
CYP inhibitory promiscuity - 0.8131 81.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6423 64.23%
Carcinogenicity (trinary) Non-required 0.7165 71.65%
Eye corrosion - 0.6389 63.89%
Eye irritation - 0.8593 85.93%
Skin irritation - 0.7981 79.81%
Skin corrosion - 0.9504 95.04%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5198 51.98%
Micronuclear - 0.7126 71.26%
Hepatotoxicity + 0.6282 62.82%
skin sensitisation - 0.8344 83.44%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.7617 76.17%
Acute Oral Toxicity (c) III 0.6641 66.41%
Estrogen receptor binding + 0.7893 78.93%
Androgen receptor binding - 0.7434 74.34%
Thyroid receptor binding - 0.5329 53.29%
Glucocorticoid receptor binding - 0.6238 62.38%
Aromatase binding - 0.7677 76.77%
PPAR gamma - 0.6111 61.11%
Honey bee toxicity - 0.6193 61.93%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.6783 67.83%

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 97.23% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.98% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.79% 85.14%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 87.03% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.05% 99.17%
CHEMBL3837 P07711 Cathepsin L 82.37% 96.61%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.65% 96.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.36% 94.80%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.89% 89.34%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.06% 94.33%

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.
Citrus × aurantium
Citrus deliciosa

Cross-Links

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PubChem 541568
NPASS NPC88519