D-threo-pentos-2-ulose

Details

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Internal ID b2c73ab7-b030-4869-b5fa-6694c09211de
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Pentoses
IUPAC Name (3S,4R)-3,4,5-trihydroxy-2-oxopentanal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H8O5/c6-1-3(8)5(10)4(9)2-7/h1,4-5,7,9-10H,2H2/t4-,5-/m1/s1
InChI Key VDSAQEDKJUSZPS-RFZPGFLSSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8O5
Molecular Weight 148.11 g/mol
Exact Mass 148.03717335 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP -2.30
Atomic LogP (AlogP) -2.53
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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Xylosone
Threo-pentos-2-ulose
D-xylosone
2-keto-D-xylose
D-lyxosone
(3S,4R)-3,4,5-trihydroxy-2-oxopentanal
26188-06-7
2-dehydro-D-xylose
threo-pentosulose
CHEBI:46675
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of D-threo-pentos-2-ulose

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5535 55.35%
Caco-2 - 0.8818 88.18%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6898 68.98%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.9442 94.42%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9763 97.63%
P-glycoprotein inhibitior - 0.9803 98.03%
P-glycoprotein substrate - 0.9782 97.82%
CYP3A4 substrate - 0.7206 72.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8124 81.24%
CYP3A4 inhibition - 0.8823 88.23%
CYP2C9 inhibition - 0.9433 94.33%
CYP2C19 inhibition - 0.9471 94.71%
CYP2D6 inhibition - 0.9460 94.60%
CYP1A2 inhibition - 0.8751 87.51%
CYP2C8 inhibition - 0.9929 99.29%
CYP inhibitory promiscuity - 0.9839 98.39%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7911 79.11%
Carcinogenicity (trinary) Non-required 0.8000 80.00%
Eye corrosion - 0.9546 95.46%
Eye irritation - 0.5834 58.34%
Skin irritation - 0.6845 68.45%
Skin corrosion - 0.9596 95.96%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8367 83.67%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.9402 94.02%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.5766 57.66%
Acute Oral Toxicity (c) III 0.4483 44.83%
Estrogen receptor binding - 0.8585 85.85%
Androgen receptor binding - 0.8385 83.85%
Thyroid receptor binding - 0.7371 73.71%
Glucocorticoid receptor binding - 0.7620 76.20%
Aromatase binding - 0.8662 86.62%
PPAR gamma - 0.8333 83.33%
Honey bee toxicity - 0.9558 95.58%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity - 0.9399 93.99%

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
CHEMBL4040 P28482 MAP kinase ERK2 92.04% 83.82%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.73% 86.92%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 86.19% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.94% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.48% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.82% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.71% 96.95%

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 160122
LOTUS LTS0263460
wikiData Q27120677