2-(Hydroxymethyl)-6-(2-hydroxy-1-methyl-4-propan-2-ylcyclohex-3-en-1-yl)oxyoxane-3,4,5-triol

Details

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Internal ID 672091f1-717f-4025-8b3d-8c9c213efb11
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name 2-(hydroxymethyl)-6-(2-hydroxy-1-methyl-4-propan-2-ylcyclohex-3-en-1-yl)oxyoxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H28O7/c1-8(2)9-4-5-16(3,11(18)6-9)23-15-14(21)13(20)12(19)10(7-17)22-15/h6,8,10-15,17-21H,4-5,7H2,1-3H3
InChI Key HDVPJYNBUXNSEW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H28O7
Molecular Weight 332.39 g/mol
Exact Mass 332.18350323 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.70
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(Hydroxymethyl)-6-(2-hydroxy-1-methyl-4-propan-2-ylcyclohex-3-en-1-yl)oxyoxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5133 51.33%
Caco-2 - 0.8312 83.12%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.8258 82.58%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.8718 87.18%
OATP1B3 inhibitior + 0.8464 84.64%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8798 87.98%
P-glycoprotein inhibitior - 0.8724 87.24%
P-glycoprotein substrate - 0.9197 91.97%
CYP3A4 substrate + 0.5515 55.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8395 83.95%
CYP3A4 inhibition - 0.8744 87.44%
CYP2C9 inhibition - 0.7067 70.67%
CYP2C19 inhibition - 0.8161 81.61%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.8085 80.85%
CYP2C8 inhibition - 0.8718 87.18%
CYP inhibitory promiscuity - 0.7819 78.19%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6854 68.54%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9873 98.73%
Skin irritation - 0.7247 72.47%
Skin corrosion - 0.9466 94.66%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5677 56.77%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.7153 71.53%
skin sensitisation - 0.8258 82.58%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.8510 85.10%
Acute Oral Toxicity (c) III 0.7210 72.10%
Estrogen receptor binding - 0.7016 70.16%
Androgen receptor binding - 0.6874 68.74%
Thyroid receptor binding + 0.6205 62.05%
Glucocorticoid receptor binding - 0.5740 57.40%
Aromatase binding + 0.5213 52.13%
PPAR gamma - 0.4923 49.23%
Honey bee toxicity - 0.7995 79.95%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.8048 80.48%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.70% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.88% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.51% 97.09%
CHEMBL2581 P07339 Cathepsin D 90.20% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.58% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.46% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.96% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 83.96% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 82.77% 94.75%

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.
Origanum vulgare

Cross-Links

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PubChem 76516447
LOTUS LTS0241754
wikiData Q105026611