Hydroxycitric acid lactone, (-)-(P)

Details

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Internal ID b5031d96-c83c-46cf-86e3-c9b5cb368319
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name 3-hydroxy-5-oxooxolane-2,3-dicarboxylic acid
SMILES (Canonical) C1C(=O)OC(C1(C(=O)O)O)C(=O)O
SMILES (Isomeric) C1C(=O)OC(C1(C(=O)O)O)C(=O)O
InChI InChI=1S/C6H6O7/c7-2-1-6(12,5(10)11)3(13-2)4(8)9/h3,12H,1H2,(H,8,9)(H,10,11)
InChI Key PFHZIWAVXDSFTB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C6H6O7
Molecular Weight 190.11 g/mol
Exact Mass 190.01135253 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP -1.20
Atomic LogP (AlogP) -1.80
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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SCHEMBL4653448
CBA75013

2D Structure

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2D Structure of Hydroxycitric acid lactone, (-)-(P)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6330 63.30%
Caco-2 - 0.9652 96.52%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6174 61.74%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.9470 94.70%
OATP1B3 inhibitior + 0.9545 95.45%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9799 97.99%
P-glycoprotein inhibitior - 0.9771 97.71%
P-glycoprotein substrate - 0.9738 97.38%
CYP3A4 substrate - 0.6359 63.59%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.8635 86.35%
CYP3A4 inhibition - 0.9388 93.88%
CYP2C9 inhibition - 0.9668 96.68%
CYP2C19 inhibition - 0.9538 95.38%
CYP2D6 inhibition - 0.9606 96.06%
CYP1A2 inhibition - 0.9621 96.21%
CYP2C8 inhibition - 0.9808 98.08%
CYP inhibitory promiscuity - 0.9927 99.27%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6197 61.97%
Eye corrosion - 0.9624 96.24%
Eye irritation + 0.7473 74.73%
Skin irritation - 0.6352 63.52%
Skin corrosion - 0.7380 73.80%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8592 85.92%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.6960 69.60%
skin sensitisation - 0.8830 88.30%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.6818 68.18%
Acute Oral Toxicity (c) III 0.5551 55.51%
Estrogen receptor binding - 0.7893 78.93%
Androgen receptor binding - 0.6923 69.23%
Thyroid receptor binding - 0.8097 80.97%
Glucocorticoid receptor binding - 0.7664 76.64%
Aromatase binding - 0.8166 81.66%
PPAR gamma - 0.6099 60.99%
Honey bee toxicity - 0.9699 96.99%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.7463 74.63%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.13% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.55% 99.23%
CHEMBL221 P23219 Cyclooxygenase-1 85.44% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.88% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 82.27% 91.19%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.43% 93.04%

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.
Garcinia cowa
Hibiscus sabdariffa

Cross-Links

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PubChem 9859390
LOTUS LTS0243890
wikiData Q105207747