(2R,3S)-4-Methylidene-5-Oxo-2-Propyloxolane-3-Carboxylic Acid

Details

Top
Internal ID 1e937f48-267a-4c4a-9a6c-d3e728cf457e
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (2R,3S)-4-methylidene-5-oxo-2-propyloxolane-3-carboxylic acid
SMILES (Canonical) CCCC1C(C(=C)C(=O)O1)C(=O)O
SMILES (Isomeric) CCC[C@@H]1[C@H](C(=C)C(=O)O1)C(=O)O
InChI InChI=1S/C9H12O4/c1-3-4-6-7(8(10)11)5(2)9(12)13-6/h6-7H,2-4H2,1H3,(H,10,11)/t6-,7+/m1/s1
InChI Key SRQUTZJZABSZRQ-RQJHMYQMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H12O4
Molecular Weight 184.19 g/mol
Exact Mass 184.07355886 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.30
Atomic LogP (AlogP) 0.97
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
SCHEMBL13535193
CHEBI:190985
BDBM50467835
MB-3, >=95% (HPLC)
NCGC00485267-01
MS-22985
PD165056
HY-129039
CS-0103268
(2R,3S)-4-methylidene-5-oxo-2-propyloxolane-3-carboxylic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of (2R,3S)-4-Methylidene-5-Oxo-2-Propyloxolane-3-Carboxylic Acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9455 94.55%
Caco-2 - 0.8013 80.13%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7263 72.63%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.8811 88.11%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9885 98.85%
P-glycoprotein inhibitior - 0.9379 93.79%
P-glycoprotein substrate - 0.9637 96.37%
CYP3A4 substrate - 0.6172 61.72%
CYP2C9 substrate + 0.6257 62.57%
CYP2D6 substrate - 0.9038 90.38%
CYP3A4 inhibition - 0.8255 82.55%
CYP2C9 inhibition - 0.8308 83.08%
CYP2C19 inhibition - 0.7601 76.01%
CYP2D6 inhibition - 0.9211 92.11%
CYP1A2 inhibition - 0.7826 78.26%
CYP2C8 inhibition - 0.9630 96.30%
CYP inhibitory promiscuity - 0.8716 87.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8943 89.43%
Carcinogenicity (trinary) Non-required 0.5626 56.26%
Eye corrosion - 0.9115 91.15%
Eye irritation + 0.9001 90.01%
Skin irritation + 0.5436 54.36%
Skin corrosion - 0.7571 75.71%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7278 72.78%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6584 65.84%
skin sensitisation - 0.7587 75.87%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5871 58.71%
Acute Oral Toxicity (c) III 0.5918 59.18%
Estrogen receptor binding - 0.5866 58.66%
Androgen receptor binding - 0.6152 61.52%
Thyroid receptor binding - 0.7253 72.53%
Glucocorticoid receptor binding - 0.7294 72.94%
Aromatase binding - 0.8082 80.82%
PPAR gamma - 0.6794 67.94%
Honey bee toxicity - 0.9546 95.46%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9262 92.62%

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
CHEMBL221 P23219 Cyclooxygenase-1 92.93% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.13% 97.25%
CHEMBL2581 P07339 Cathepsin D 87.56% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.19% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.89% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.16% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.33% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.66% 95.50%
CHEMBL4040 P28482 MAP kinase ERK2 80.39% 83.82%

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.
Carthamus arborescens

Cross-Links

Top
PubChem 21579153
NPASS NPC48641
LOTUS LTS0009068
wikiData Q105259365