alpha-Hydroxycitric acid

Details

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Internal ID dd5c5fad-f6a5-49d6-b4d5-2c7eefd954e4
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name 2-hydroperoxypropane-1,2,3-tricarboxylic acid
SMILES (Canonical) C(C(=O)O)C(CC(=O)O)(C(=O)O)OO
SMILES (Isomeric) C(C(=O)O)C(CC(=O)O)(C(=O)O)OO
InChI InChI=1S/C6H8O8/c7-3(8)1-6(14-13,5(11)12)2-4(9)10/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)
InChI Key OIPKKHARWZNZEQ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C6H8O8
Molecular Weight 208.12 g/mol
Exact Mass 208.02191721 g/mol
Topological Polar Surface Area (TPSA) 141.00 Ų
XlogP -2.00
Atomic LogP (AlogP) -0.75
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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SCHEMBL108616

2D Structure

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2D Structure of alpha-Hydroxycitric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7722 77.22%
Caco-2 - 0.8375 83.75%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7786 77.86%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.9506 95.06%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9829 98.29%
P-glycoprotein inhibitior - 0.9807 98.07%
P-glycoprotein substrate - 0.9961 99.61%
CYP3A4 substrate - 0.7314 73.14%
CYP2C9 substrate + 0.6406 64.06%
CYP2D6 substrate - 0.8605 86.05%
CYP3A4 inhibition - 0.9148 91.48%
CYP2C9 inhibition - 0.9134 91.34%
CYP2C19 inhibition - 0.9059 90.59%
CYP2D6 inhibition - 0.9313 93.13%
CYP1A2 inhibition - 0.9292 92.92%
CYP2C8 inhibition - 0.9800 98.00%
CYP inhibitory promiscuity - 0.9722 97.22%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7130 71.30%
Carcinogenicity (trinary) Non-required 0.6650 66.50%
Eye corrosion - 0.6285 62.85%
Eye irritation + 0.9301 93.01%
Skin irritation - 0.6845 68.45%
Skin corrosion - 0.6359 63.59%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7479 74.79%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.6431 64.31%
skin sensitisation - 0.7689 76.89%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6849 68.49%
Acute Oral Toxicity (c) III 0.7963 79.63%
Estrogen receptor binding - 0.9081 90.81%
Androgen receptor binding - 0.7012 70.12%
Thyroid receptor binding - 0.8558 85.58%
Glucocorticoid receptor binding - 0.7105 71.05%
Aromatase binding - 0.6690 66.90%
PPAR gamma - 0.8027 80.27%
Honey bee toxicity - 0.9322 93.22%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.7345 73.45%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.54% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.54% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.20% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.65% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.51% 85.14%

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
Garcinia gummi-gutta

Cross-Links

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PubChem 57473313
LOTUS LTS0251138
wikiData Q104251587