7-Deoxy-sedoheptulose

Details

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Internal ID 5ad10411-72bd-4b60-bb2e-e8c2edc22563
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > C-glycosyl compounds
IUPAC Name 5-(1-hydroxyethyl)-2-(hydroxymethyl)oxolane-2,3,4-triol
SMILES (Canonical) CC(C1C(C(C(O1)(CO)O)O)O)O
SMILES (Isomeric) CC(C1C(C(C(O1)(CO)O)O)O)O
InChI InChI=1S/C7H14O6/c1-3(9)5-4(10)6(11)7(12,2-8)13-5/h3-6,8-12H,2H2,1H3
InChI Key AVRKQOKNQSVQNT-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C7H14O6
Molecular Weight 194.18 g/mol
Exact Mass 194.07903816 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP -1.90
Atomic LogP (AlogP) -2.83
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Deoxy-sedoheptulose

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8235 82.35%
Caco-2 - 0.9338 93.38%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6050 60.50%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.9504 95.04%
OATP1B3 inhibitior + 0.9601 96.01%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9823 98.23%
P-glycoprotein inhibitior - 0.9719 97.19%
P-glycoprotein substrate - 0.9064 90.64%
CYP3A4 substrate - 0.6286 62.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8405 84.05%
CYP3A4 inhibition - 0.9777 97.77%
CYP2C9 inhibition - 0.9555 95.55%
CYP2C19 inhibition - 0.9547 95.47%
CYP2D6 inhibition - 0.9659 96.59%
CYP1A2 inhibition - 0.9385 93.85%
CYP2C8 inhibition - 0.9827 98.27%
CYP inhibitory promiscuity - 0.9622 96.22%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6632 66.32%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.9800 98.00%
Skin irritation - 0.7986 79.86%
Skin corrosion - 0.9159 91.59%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6590 65.90%
Micronuclear - 0.7667 76.67%
Hepatotoxicity - 0.6198 61.98%
skin sensitisation - 0.9338 93.38%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.7263 72.63%
Acute Oral Toxicity (c) IV 0.5852 58.52%
Estrogen receptor binding - 0.7679 76.79%
Androgen receptor binding - 0.8571 85.71%
Thyroid receptor binding - 0.6067 60.67%
Glucocorticoid receptor binding - 0.7928 79.28%
Aromatase binding - 0.8244 82.44%
PPAR gamma - 0.7973 79.73%
Honey bee toxicity - 0.9363 93.63%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity - 0.9164 91.64%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.11% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.45% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.32% 97.25%
CHEMBL2581 P07339 Cathepsin D 89.25% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.86% 85.14%
CHEMBL226 P30542 Adenosine A1 receptor 88.08% 95.93%
CHEMBL2996 Q05655 Protein kinase C delta 84.56% 97.79%

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 146683588
LOTUS LTS0139769
wikiData Q104919760