beta-Glycerophosphoric acid

Details

Top
Internal ID 0b6b168a-533d-4892-b159-b032e43fd5e9
Taxonomy Lipids and lipid-like molecules > Glycerophospholipids > Glycerophosphates
IUPAC Name 1,3-dihydroxypropan-2-yl dihydrogen phosphate
SMILES (Canonical) C(C(CO)OP(=O)(O)O)O
SMILES (Isomeric) C(C(CO)OP(=O)(O)O)O
InChI InChI=1S/C3H9O6P/c4-1-3(2-5)9-10(6,7)8/h3-5H,1-2H2,(H2,6,7,8)
InChI Key DHCLVCXQIBBOPH-UHFFFAOYSA-N
Popularity 1,018 references in papers

Physical and Chemical Properties

Top
Molecular Formula C3H9O6P
Molecular Weight 172.07 g/mol
Exact Mass 172.01367500 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP -2.90
Atomic LogP (AlogP) -1.55
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

Top
beta-glycerophosphate
17181-54-3
Glycerol 2-phosphate
1,2,3-Propanetriol, 2-(dihydrogen phosphate)
GLYCEROL-2-PHOSPHATE
1,3-Hydroxy-2-propyl dihydrogen phosphate
Glycerophosphoric acid II
2-glycerophosphate
1,3-dihydroxypropan-2-yl dihydrogen phosphate
glyceryl 2-phosphate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of beta-Glycerophosphoric acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9406 94.06%
Caco-2 - 0.8768 87.68%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7831 78.31%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.9666 96.66%
OATP1B3 inhibitior + 0.9442 94.42%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9649 96.49%
P-glycoprotein inhibitior - 0.9735 97.35%
P-glycoprotein substrate - 0.9898 98.98%
CYP3A4 substrate - 0.6875 68.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8128 81.28%
CYP3A4 inhibition - 0.9549 95.49%
CYP2C9 inhibition - 0.8902 89.02%
CYP2C19 inhibition - 0.8692 86.92%
CYP2D6 inhibition - 0.9214 92.14%
CYP1A2 inhibition - 0.9102 91.02%
CYP2C8 inhibition - 0.9925 99.25%
CYP inhibitory promiscuity - 0.9313 93.13%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.7508 75.08%
Carcinogenicity (trinary) Non-required 0.5496 54.96%
Eye corrosion - 0.7013 70.13%
Eye irritation - 0.8076 80.76%
Skin irritation - 0.7309 73.09%
Skin corrosion - 0.6205 62.05%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6249 62.49%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.7197 71.97%
skin sensitisation - 0.8686 86.86%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.7085 70.85%
Acute Oral Toxicity (c) III 0.6211 62.11%
Estrogen receptor binding - 0.9062 90.62%
Androgen receptor binding - 0.8073 80.73%
Thyroid receptor binding - 0.8032 80.32%
Glucocorticoid receptor binding - 0.8649 86.49%
Aromatase binding - 0.7093 70.93%
PPAR gamma - 0.7855 78.55%
Honey bee toxicity - 0.4671 46.71%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8155 81.55%
Fish aquatic toxicity - 0.8967 89.67%

Targets

Top

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 95.02% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.38% 96.09%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 86.02% 94.01%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.77% 91.71%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.76% 95.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.35% 96.95%

Plants that contains it

Top
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
Solanum lycopersicum

Cross-Links

Top
PubChem 2526
NPASS NPC31433
LOTUS LTS0006225
wikiData Q21099098