5-(1,3-Dihydroxy-2-methylbutyl)-4-hydroxy-3,5-dimethyloxolan-2-one

Details

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Internal ID 6d83615f-1f48-4bf3-a81f-7fcc854ed253
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 5-(1,3-dihydroxy-2-methylbutyl)-4-hydroxy-3,5-dimethyloxolan-2-one
SMILES (Canonical) CC1C(C(OC1=O)(C)C(C(C)C(C)O)O)O
SMILES (Isomeric) CC1C(C(OC1=O)(C)C(C(C)C(C)O)O)O
InChI InChI=1S/C11H20O5/c1-5(7(3)12)8(13)11(4)9(14)6(2)10(15)16-11/h5-9,12-14H,1-4H3
InChI Key HNZKRSKSIABLNS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20O5
Molecular Weight 232.27 g/mol
Exact Mass 232.13107373 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 0.50
Atomic LogP (AlogP) -0.32
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(1,3-Dihydroxy-2-methylbutyl)-4-hydroxy-3,5-dimethyloxolan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7569 75.69%
Caco-2 - 0.6484 64.84%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6444 64.44%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.9230 92.30%
OATP1B3 inhibitior + 0.9356 93.56%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9381 93.81%
P-glycoprotein inhibitior - 0.9470 94.70%
P-glycoprotein substrate - 0.8971 89.71%
CYP3A4 substrate - 0.5422 54.22%
CYP2C9 substrate - 0.7919 79.19%
CYP2D6 substrate - 0.8704 87.04%
CYP3A4 inhibition - 0.8948 89.48%
CYP2C9 inhibition - 0.9481 94.81%
CYP2C19 inhibition - 0.9584 95.84%
CYP2D6 inhibition - 0.9598 95.98%
CYP1A2 inhibition - 0.8838 88.38%
CYP2C8 inhibition - 0.9868 98.68%
CYP inhibitory promiscuity - 0.9077 90.77%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5558 55.58%
Eye corrosion - 0.9092 90.92%
Eye irritation - 0.9622 96.22%
Skin irritation - 0.6635 66.35%
Skin corrosion - 0.8778 87.78%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8003 80.03%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.5158 51.58%
skin sensitisation - 0.8231 82.31%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.5821 58.21%
Nephrotoxicity + 0.6664 66.64%
Acute Oral Toxicity (c) III 0.6340 63.40%
Estrogen receptor binding - 0.6139 61.39%
Androgen receptor binding - 0.6336 63.36%
Thyroid receptor binding + 0.5505 55.05%
Glucocorticoid receptor binding - 0.6455 64.55%
Aromatase binding - 0.7494 74.94%
PPAR gamma - 0.7150 71.50%
Honey bee toxicity - 0.8568 85.68%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.5965 59.65%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.17% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.80% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.14% 85.14%
CHEMBL2581 P07339 Cathepsin D 93.24% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.80% 96.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 86.42% 96.47%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.22% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.27% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.77% 97.14%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.14% 92.88%
CHEMBL3401 O75469 Pregnane X receptor 80.62% 94.73%

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 75215424
LOTUS LTS0230842
wikiData Q104168041