2,3-Diphosphoglyceric Acid

Details

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Internal ID 2fa2c566-9168-4a1d-b0d5-30f07e9853a7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Sugar acids and derivatives
IUPAC Name (2R)-2,3-diphosphonooxypropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C3H8O10P2/c4-3(5)2(13-15(9,10)11)1-12-14(6,7)8/h2H,1H2,(H,4,5)(H2,6,7,8)(H2,9,10,11)/t2-/m1/s1
InChI Key XOHUEYCVLUUEJJ-UWTATZPHSA-N
Popularity 1,452 references in papers

Physical and Chemical Properties

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Molecular Formula C3H8O10P2
Molecular Weight 266.04 g/mol
Exact Mass 265.95927044 g/mol
Topological Polar Surface Area (TPSA) 171.00 Ų
XlogP -3.70
Atomic LogP (AlogP) -1.34
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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(2R)-2,3-bis(phosphonooxy)propanoic acid
RefChem:908666
GlyTouCan:G13685BJ
2,3 Diphosphoglyceric Acid
G13685BJ
2,3-bisphospho-D-glycerate
D-greenwald ester
14438-19-8
(2R)-2,3-diphosphonooxypropanoic acid
2,3-Bisphospho-D-glyceric acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,3-Diphosphoglyceric Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8857 88.57%
Caco-2 - 0.9668 96.68%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8930 89.30%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9601 96.01%
OATP1B3 inhibitior + 0.9438 94.38%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9655 96.55%
P-glycoprotein inhibitior - 0.9443 94.43%
P-glycoprotein substrate - 0.9688 96.88%
CYP3A4 substrate - 0.6587 65.87%
CYP2C9 substrate + 0.5963 59.63%
CYP2D6 substrate - 0.8830 88.30%
CYP3A4 inhibition - 0.9697 96.97%
CYP2C9 inhibition - 0.9126 91.26%
CYP2C19 inhibition - 0.9029 90.29%
CYP2D6 inhibition - 0.9232 92.32%
CYP1A2 inhibition - 0.9301 93.01%
CYP2C8 inhibition - 0.9879 98.79%
CYP inhibitory promiscuity - 0.9798 97.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7411 74.11%
Carcinogenicity (trinary) Non-required 0.5822 58.22%
Eye corrosion + 0.5128 51.28%
Eye irritation - 0.8792 87.92%
Skin irritation - 0.7174 71.74%
Skin corrosion + 0.5420 54.20%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7067 70.67%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.5474 54.74%
skin sensitisation - 0.8575 85.75%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6048 60.48%
Acute Oral Toxicity (c) III 0.6242 62.42%
Estrogen receptor binding - 0.5844 58.44%
Androgen receptor binding + 0.5204 52.04%
Thyroid receptor binding - 0.6785 67.85%
Glucocorticoid receptor binding - 0.7209 72.09%
Aromatase binding - 0.7547 75.47%
PPAR gamma - 0.7195 71.95%
Honey bee toxicity - 0.5143 51.43%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7655 76.55%
Fish aquatic toxicity - 0.4376 43.76%

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 94.91% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.41% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 92.47% 83.82%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 89.88% 91.71%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 89.31% 94.01%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.40% 95.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.10% 99.17%

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 186004
LOTUS LTS0232142
wikiData Q27102555