(4S)-3,5,5-Trimethyl-4-(beta-D-glucopyranosyloxy)-2-cyclohexen-1-one

Details

Top
Internal ID 65a3c877-0b2d-44ea-a66f-1990d708e301
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (4S)-3,5,5-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohex-2-en-1-one
SMILES (Canonical) CC1=CC(=O)CC(C1OC2C(C(C(C(O2)CO)O)O)O)(C)C
SMILES (Isomeric) CC1=CC(=O)CC([C@@H]1O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)(C)C
InChI InChI=1S/C15H24O7/c1-7-4-8(17)5-15(2,3)13(7)22-14-12(20)11(19)10(18)9(6-16)21-14/h4,9-14,16,18-20H,5-6H2,1-3H3/t9-,10-,11+,12-,13-,14+/m1/s1
InChI Key SCGSEQMMGAPFBT-WNWFYDSVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24O7
Molecular Weight 316.35 g/mol
Exact Mass 316.15220310 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP -1.10
Atomic LogP (AlogP) -0.88
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (4S)-3,5,5-Trimethyl-4-(beta-D-glucopyranosyloxy)-2-cyclohexen-1-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5080 50.80%
Caco-2 - 0.7521 75.21%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.8414 84.14%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.8975 89.75%
OATP1B3 inhibitior + 0.8949 89.49%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8274 82.74%
P-glycoprotein inhibitior - 0.8483 84.83%
P-glycoprotein substrate - 0.9500 95.00%
CYP3A4 substrate + 0.5742 57.42%
CYP2C9 substrate - 0.7960 79.60%
CYP2D6 substrate - 0.8805 88.05%
CYP3A4 inhibition - 0.9065 90.65%
CYP2C9 inhibition - 0.7380 73.80%
CYP2C19 inhibition - 0.8087 80.87%
CYP2D6 inhibition - 0.9276 92.76%
CYP1A2 inhibition - 0.8129 81.29%
CYP2C8 inhibition - 0.9185 91.85%
CYP inhibitory promiscuity - 0.7509 75.09%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6473 64.73%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9801 98.01%
Skin irritation - 0.7989 79.89%
Skin corrosion - 0.9596 95.96%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5213 52.13%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.7758 77.58%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.4737 47.37%
Acute Oral Toxicity (c) III 0.7159 71.59%
Estrogen receptor binding - 0.5683 56.83%
Androgen receptor binding - 0.5882 58.82%
Thyroid receptor binding - 0.5562 55.62%
Glucocorticoid receptor binding - 0.4752 47.52%
Aromatase binding - 0.6623 66.23%
PPAR gamma - 0.6037 60.37%
Honey bee toxicity - 0.8867 88.67%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7250 72.50%
Fish aquatic toxicity + 0.8263 82.63%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.98% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.51% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.22% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.95% 95.56%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.39% 96.21%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.65% 97.25%
CHEMBL2581 P07339 Cathepsin D 86.15% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.47% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.90% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 83.76% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.66% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.46% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.60% 94.45%
CHEMBL220 P22303 Acetylcholinesterase 80.39% 94.45%

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.
Crocus sativus

Cross-Links

Top
PubChem 101706277
LOTUS LTS0255155
wikiData Q105250115