(2R,3R,5S)-5-(carboxymethyl)-2,3,5-trimethyloxolane-2-carboxylic acid

Details

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Internal ID 4da0f518-18a1-4054-b5f4-63c80f500096
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Dicarboxylic acids and derivatives
IUPAC Name (2R,3R,5S)-5-(carboxymethyl)-2,3,5-trimethyloxolane-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O5/c1-6-4-9(2,5-7(11)12)15-10(6,3)8(13)14/h6H,4-5H2,1-3H3,(H,11,12)(H,13,14)/t6-,9+,10-/m1/s1
InChI Key MCGQKNRASJPXNC-WHFVKQHSSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O5
Molecular Weight 216.23 g/mol
Exact Mass 216.09977361 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.12
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R,5S)-5-(carboxymethyl)-2,3,5-trimethyloxolane-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8160 81.60%
Caco-2 + 0.6054 60.54%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6128 61.28%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9312 93.12%
OATP1B3 inhibitior + 0.9345 93.45%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8636 86.36%
P-glycoprotein inhibitior - 0.9739 97.39%
P-glycoprotein substrate - 0.9216 92.16%
CYP3A4 substrate - 0.5477 54.77%
CYP2C9 substrate + 0.6594 65.94%
CYP2D6 substrate - 0.8854 88.54%
CYP3A4 inhibition - 0.8490 84.90%
CYP2C9 inhibition - 0.9026 90.26%
CYP2C19 inhibition - 0.8996 89.96%
CYP2D6 inhibition - 0.9573 95.73%
CYP1A2 inhibition - 0.8541 85.41%
CYP2C8 inhibition - 0.9467 94.67%
CYP inhibitory promiscuity - 0.9505 95.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6077 60.77%
Eye corrosion - 0.9370 93.70%
Eye irritation - 0.6447 64.47%
Skin irritation - 0.6068 60.68%
Skin corrosion - 0.8544 85.44%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8104 81.04%
Micronuclear - 0.7041 70.41%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.7108 71.08%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6029 60.29%
Acute Oral Toxicity (c) III 0.5793 57.93%
Estrogen receptor binding - 0.7106 71.06%
Androgen receptor binding - 0.7786 77.86%
Thyroid receptor binding - 0.7486 74.86%
Glucocorticoid receptor binding - 0.8052 80.52%
Aromatase binding - 0.7918 79.18%
PPAR gamma - 0.8416 84.16%
Honey bee toxicity - 0.9548 95.48%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.7005 70.05%

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 94.81% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 91.50% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.77% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.15% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 85.43% 91.19%

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.
Senecio nemorensis

Cross-Links

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PubChem 10965923
LOTUS LTS0132295
wikiData Q105161187