Prelactone B

Details

Top
Internal ID 196a8b51-c9de-44e5-ab6e-c92c74f9efe0
Taxonomy Organoheterocyclic compounds > Lactones > Delta valerolactones
IUPAC Name (4R,5S,6R)-4-hydroxy-5-methyl-6-propan-2-yloxan-2-one
SMILES (Canonical) CC1C(CC(=O)OC1C(C)C)O
SMILES (Isomeric) C[C@H]1[C@@H](CC(=O)O[C@@H]1C(C)C)O
InChI InChI=1S/C9H16O3/c1-5(2)9-6(3)7(10)4-8(11)12-9/h5-7,9-10H,4H2,1-3H3/t6-,7+,9+/m0/s1
InChI Key GZGROEXVPWSNDV-LKEWCRSYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H16O3
Molecular Weight 172.22 g/mol
Exact Mass 172.109944368 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.40
Atomic LogP (AlogP) 0.95
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
147659-07-2
(4R,5S,6R)-4-Hydroxy-5-methyl-6-propan-2-yloxan-2-one
2H-Pyran-2-one,tetrahydro-4-hydroxy-5-methyl-6-(1-methylethyl)-,(4R,5S,6R)-(9CI)

2D Structure

Top
2D Structure of Prelactone B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9825 98.25%
Caco-2 - 0.5362 53.62%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7798 77.98%
OATP2B1 inhibitior - 0.8461 84.61%
OATP1B1 inhibitior + 0.9345 93.45%
OATP1B3 inhibitior + 0.9732 97.32%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9716 97.16%
P-glycoprotein inhibitior - 0.9371 93.71%
P-glycoprotein substrate - 0.9460 94.60%
CYP3A4 substrate - 0.5982 59.82%
CYP2C9 substrate - 0.5888 58.88%
CYP2D6 substrate - 0.8457 84.57%
CYP3A4 inhibition - 0.9736 97.36%
CYP2C9 inhibition - 0.9801 98.01%
CYP2C19 inhibition - 0.9662 96.62%
CYP2D6 inhibition - 0.9631 96.31%
CYP1A2 inhibition - 0.9528 95.28%
CYP2C8 inhibition - 0.9944 99.44%
CYP inhibitory promiscuity - 0.9926 99.26%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.8428 84.28%
Carcinogenicity (trinary) Non-required 0.7342 73.42%
Eye corrosion - 0.7937 79.37%
Eye irritation + 0.5379 53.79%
Skin irritation + 0.6939 69.39%
Skin corrosion - 0.8230 82.30%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7042 70.42%
Micronuclear - 0.6141 61.41%
Hepatotoxicity + 0.6730 67.30%
skin sensitisation - 0.8054 80.54%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.6110 61.10%
Acute Oral Toxicity (c) III 0.7222 72.22%
Estrogen receptor binding - 0.7118 71.18%
Androgen receptor binding - 0.8292 82.92%
Thyroid receptor binding - 0.7813 78.13%
Glucocorticoid receptor binding - 0.8871 88.71%
Aromatase binding - 0.8670 86.70%
PPAR gamma - 0.8016 80.16%
Honey bee toxicity - 0.8797 87.97%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5450 54.50%
Fish aquatic toxicity - 0.6565 65.65%

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
CHEMBL2581 P07339 Cathepsin D 92.97% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.25% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.38% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.12% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.03% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.02% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.52% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.30% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.19% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 81.74% 94.73%

Cross-Links

Top
PubChem 11105821
NPASS NPC103557
LOTUS LTS0180074
wikiData Q104402053