1-Deoxy-D-manno-heptulose

Details

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Internal ID 422e5c13-0c3b-4f94-9cb7-ed4fe7713be5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Heptoses
IUPAC Name 3,4,5,6,7-pentahydroxyheptan-2-one
SMILES (Canonical) CC(=O)C(C(C(C(CO)O)O)O)O
SMILES (Isomeric) CC(=O)C(C(C(C(CO)O)O)O)O
InChI InChI=1S/C7H14O6/c1-3(9)5(11)7(13)6(12)4(10)2-8/h4-8,10-13H,2H2,1H3
InChI Key OUSKVHOYPHDTIA-UHFFFAOYSA-N
Popularity 2 references 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) 118.00 Ų
XlogP -3.20
Atomic LogP (AlogP) -2.99
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Deoxy-D-manno-heptulose

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5574 55.74%
Caco-2 - 0.9591 95.91%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7101 71.01%
OATP2B1 inhibitior - 0.8562 85.62%
OATP1B1 inhibitior + 0.9589 95.89%
OATP1B3 inhibitior + 0.9418 94.18%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9717 97.17%
P-glycoprotein inhibitior - 0.9788 97.88%
P-glycoprotein substrate - 0.9383 93.83%
CYP3A4 substrate - 0.6797 67.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8120 81.20%
CYP3A4 inhibition - 0.9157 91.57%
CYP2C9 inhibition - 0.9339 93.39%
CYP2C19 inhibition - 0.9461 94.61%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.8680 86.80%
CYP2C8 inhibition - 0.9947 99.47%
CYP inhibitory promiscuity - 0.9653 96.53%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.7952 79.52%
Eye corrosion - 0.9830 98.30%
Eye irritation - 0.9798 97.98%
Skin irritation - 0.7505 75.05%
Skin corrosion - 0.9329 93.29%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7105 71.05%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.8750 87.50%
skin sensitisation - 0.9486 94.86%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.8830 88.30%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.6062 60.62%
Acute Oral Toxicity (c) IV 0.7280 72.80%
Estrogen receptor binding - 0.8160 81.60%
Androgen receptor binding - 0.8302 83.02%
Thyroid receptor binding - 0.6330 63.30%
Glucocorticoid receptor binding - 0.6084 60.84%
Aromatase binding - 0.8765 87.65%
PPAR gamma - 0.8921 89.21%
Honey bee toxicity - 0.9733 97.33%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.9500 95.00%
Fish aquatic toxicity - 0.9515 95.15%

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 94.52% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.68% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.63% 85.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.31% 96.95%
CHEMBL4040 P28482 MAP kinase ERK2 82.15% 83.82%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.70% 98.75%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.44% 97.29%

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 13632470
LOTUS LTS0093886
wikiData Q105200390