6-deoxy-3-O-methyl-allose

Details

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Internal ID 727554bf-9611-4da2-af4d-9d529d1b8a4e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (2R,3R,4R,5R)-2,4,5-trihydroxy-3-methoxyhexanal
SMILES (Canonical) CC(C(C(C(C=O)O)OC)O)O
SMILES (Isomeric) C[C@H]([C@H]([C@H]([C@H](C=O)O)OC)O)O
InChI InChI=1S/C7H14O5/c1-4(9)6(11)7(12-2)5(10)3-8/h3-7,9-11H,1-2H3/t4-,5+,6-,7+/m1/s1
InChI Key MPQBLCRFUYGBHE-UCROKIRRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C7H14O5
Molecular Weight 178.18 g/mol
Exact Mass 178.08412354 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP -1.80
Atomic LogP (AlogP) -1.70
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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SCHEMBL1406099

2D Structure

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2D Structure of 6-deoxy-3-O-methyl-allose

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7399 73.99%
Caco-2 - 0.8443 84.43%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7392 73.92%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.9376 93.76%
OATP1B3 inhibitior + 0.9669 96.69%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9756 97.56%
P-glycoprotein inhibitior - 0.9652 96.52%
P-glycoprotein substrate - 0.9711 97.11%
CYP3A4 substrate - 0.6282 62.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7997 79.97%
CYP3A4 inhibition - 0.8698 86.98%
CYP2C9 inhibition - 0.8561 85.61%
CYP2C19 inhibition - 0.8957 89.57%
CYP2D6 inhibition - 0.9258 92.58%
CYP1A2 inhibition - 0.8759 87.59%
CYP2C8 inhibition - 0.9844 98.44%
CYP inhibitory promiscuity - 0.9194 91.94%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.6123 61.23%
Carcinogenicity (trinary) Non-required 0.7699 76.99%
Eye corrosion - 0.8759 87.59%
Eye irritation - 0.9395 93.95%
Skin irritation - 0.6506 65.06%
Skin corrosion - 0.9132 91.32%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7247 72.47%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8329 83.29%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.7914 79.14%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.7694 76.94%
Acute Oral Toxicity (c) III 0.7090 70.90%
Estrogen receptor binding - 0.7164 71.64%
Androgen receptor binding - 0.9031 90.31%
Thyroid receptor binding - 0.6100 61.00%
Glucocorticoid receptor binding - 0.7312 73.12%
Aromatase binding - 0.8700 87.00%
PPAR gamma - 0.8383 83.83%
Honey bee toxicity - 0.6624 66.24%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.8681 86.81%

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 92.05% 96.09%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.54% 90.24%
CHEMBL2581 P07339 Cathepsin D 85.18% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.27% 85.14%
CHEMBL4208 P20618 Proteasome component C5 82.39% 90.00%

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.
Hoya carnosa

Cross-Links

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PubChem 12358612
LOTUS LTS0121687
wikiData Q105169673