Glyceraldehyde-3-phosphate

Details

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Internal ID b34c72af-242e-48f6-a408-37de79f87d2e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Monosaccharide phosphates > Glyceraldehyde-3-phosphates
IUPAC Name [(2R)-2-hydroxy-3-oxopropyl] dihydrogen phosphate
SMILES (Canonical) C(C(C=O)O)OP(=O)(O)O
SMILES (Isomeric) C([C@H](C=O)O)OP(=O)(O)O
InChI InChI=1S/C3H7O6P/c4-1-3(5)2-9-10(6,7)8/h1,3,5H,2H2,(H2,6,7,8)/t3-/m0/s1
InChI Key LXJXRIRHZLFYRP-VKHMYHEASA-N
Popularity 694 references in papers

Physical and Chemical Properties

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Molecular Formula C3H7O6P
Molecular Weight 170.06 g/mol
Exact Mass 169.99802494 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP -2.70
Atomic LogP (AlogP) -1.34
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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591-57-1
glyceraldehyde-3-phosphate
Triose phosphate
D-glyceraldehyde-3-phosphate
propanal, 2-hydroxy-3-(phosphonooxy)-, (2R)-
glyceraldehyde-P
TD9ZNF8JPW
[(2R)-2-hydroxy-3-oxopropyl] dihydrogen phosphate
3-Phosphoglyceraldehyde, D-
(2R)-2-Hydroxy-3-(phosphonooxy)-propanal
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Glyceraldehyde-3-phosphate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7475 74.75%
Caco-2 - 0.8495 84.95%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.8760 87.60%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.9442 94.42%
OATP1B3 inhibitior + 0.9440 94.40%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9626 96.26%
P-glycoprotein inhibitior - 0.9810 98.10%
P-glycoprotein substrate - 0.9752 97.52%
CYP3A4 substrate - 0.6366 63.66%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.7908 79.08%
CYP3A4 inhibition - 0.9694 96.94%
CYP2C9 inhibition - 0.9253 92.53%
CYP2C19 inhibition - 0.9096 90.96%
CYP2D6 inhibition - 0.9322 93.22%
CYP1A2 inhibition - 0.9400 94.00%
CYP2C8 inhibition - 0.9822 98.22%
CYP inhibitory promiscuity - 0.9806 98.06%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.6819 68.19%
Carcinogenicity (trinary) Non-required 0.5963 59.63%
Eye corrosion + 0.6993 69.93%
Eye irritation - 0.5424 54.24%
Skin irritation - 0.6855 68.55%
Skin corrosion + 0.6844 68.44%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6915 69.15%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.5440 54.40%
skin sensitisation - 0.8466 84.66%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6542 65.42%
Estrogen receptor binding - 0.5762 57.62%
Androgen receptor binding - 0.7586 75.86%
Thyroid receptor binding - 0.7226 72.26%
Glucocorticoid receptor binding - 0.6221 62.21%
Aromatase binding - 0.7905 79.05%
PPAR gamma - 0.8021 80.21%
Honey bee toxicity + 0.6611 66.11%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.6949 69.49%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 97.17% 97.29%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 93.46% 94.01%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.41% 96.09%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 89.02% 91.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.79% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 81.03% 94.73%
CHEMBL1900 P15121 Aldose reductase 80.28% 92.38%

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.
Arabidopsis thaliana
Vigna radiata

Cross-Links

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PubChem 439168
LOTUS LTS0148103
wikiData Q26992303