4-Fluoro-2,3,5,6-tetrahydroxyhexanoic acid

Details

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Internal ID 92ce3c57-6966-449e-b569-c025c1b219bd
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name 4-fluoro-2,3,5,6-tetrahydroxyhexanoic acid
SMILES (Canonical) C(C(C(C(C(C(=O)O)O)O)F)O)O
SMILES (Isomeric) C(C(C(C(C(C(=O)O)O)O)F)O)O
InChI InChI=1S/C6H11FO6/c7-3(2(9)1-8)4(10)5(11)6(12)13/h2-5,8-11H,1H2,(H,12,13)
InChI Key OPDFEMUVZDUCJR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11FO6
Molecular Weight 198.15 g/mol
Exact Mass 198.05396623 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP -2.30
Atomic LogP (AlogP) -2.52
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Fluoro-2,3,5,6-tetrahydroxyhexanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5904 59.04%
Caco-2 - 0.9659 96.59%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7237 72.37%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.9535 95.35%
OATP1B3 inhibitior + 0.9298 92.98%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9523 95.23%
P-glycoprotein inhibitior - 0.9869 98.69%
P-glycoprotein substrate - 0.9708 97.08%
CYP3A4 substrate - 0.7036 70.36%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate - 0.8591 85.91%
CYP3A4 inhibition - 0.8382 83.82%
CYP2C9 inhibition - 0.9093 90.93%
CYP2C19 inhibition - 0.9008 90.08%
CYP2D6 inhibition - 0.9094 90.94%
CYP1A2 inhibition - 0.8725 87.25%
CYP2C8 inhibition - 0.9782 97.82%
CYP inhibitory promiscuity - 0.9648 96.48%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7944 79.44%
Carcinogenicity (trinary) Non-required 0.7353 73.53%
Eye corrosion - 0.9614 96.14%
Eye irritation - 0.9191 91.91%
Skin irritation - 0.6631 66.31%
Skin corrosion - 0.8702 87.02%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8126 81.26%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.9065 90.65%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.5413 54.13%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.4804 48.04%
Acute Oral Toxicity (c) III 0.4942 49.42%
Estrogen receptor binding - 0.8455 84.55%
Androgen receptor binding - 0.7660 76.60%
Thyroid receptor binding - 0.5425 54.25%
Glucocorticoid receptor binding + 0.5418 54.18%
Aromatase binding - 0.8813 88.13%
PPAR gamma - 0.7713 77.13%
Honey bee toxicity - 0.9563 95.63%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.8591 85.91%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.76% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.95% 96.09%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 90.34% 98.75%
CHEMBL221 P23219 Cyclooxygenase-1 86.90% 90.17%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 86.73% 97.34%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.11% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.79% 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 162926816
LOTUS LTS0123379
wikiData Q105195990