2-amino-2,3,7-trideoxy-D-lyxo-hept-6-ulosonic acid

Details

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Internal ID 5348af66-7d4d-42b7-bb54-cbb14e25bb99
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > L-alpha-amino acids
IUPAC Name (2S,4R,5S)-2-amino-4,5-dihydroxy-6-oxoheptanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H13NO5/c1-3(9)6(11)5(10)2-4(8)7(12)13/h4-6,10-11H,2,8H2,1H3,(H,12,13)/t4-,5+,6+/m0/s1
InChI Key IFMHGOADXGYWMO-KVQBGUIXSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C7H13NO5
Molecular Weight 191.18 g/mol
Exact Mass 191.07937252 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP -4.50
Atomic LogP (AlogP) -1.90
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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2-amino-2,3,7-trideoxy-D-lyxo-hept-6-ulosonic acid
CHEBI:51282
LMFA01050473
Q27122518
(2S,4R,5S)-2-amino-4,5-dihydroxy-6-oxoheptanoic acid

2D Structure

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2D Structure of 2-amino-2,3,7-trideoxy-D-lyxo-hept-6-ulosonic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6062 60.62%
Caco-2 - 0.9761 97.61%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.4088 40.88%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9570 95.70%
OATP1B3 inhibitior + 0.9106 91.06%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9685 96.85%
P-glycoprotein inhibitior - 0.9866 98.66%
P-glycoprotein substrate - 0.9338 93.38%
CYP3A4 substrate - 0.7166 71.66%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.7946 79.46%
CYP3A4 inhibition - 0.9185 91.85%
CYP2C9 inhibition - 0.9420 94.20%
CYP2C19 inhibition - 0.9544 95.44%
CYP2D6 inhibition - 0.9440 94.40%
CYP1A2 inhibition - 0.9092 90.92%
CYP2C8 inhibition - 0.9832 98.32%
CYP inhibitory promiscuity - 0.9939 99.39%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6593 65.93%
Eye corrosion - 0.9823 98.23%
Eye irritation - 0.9456 94.56%
Skin irritation - 0.8415 84.15%
Skin corrosion - 0.9576 95.76%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8202 82.02%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.6175 61.75%
skin sensitisation - 0.9472 94.72%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.8087 80.87%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.6767 67.67%
Acute Oral Toxicity (c) III 0.5777 57.77%
Estrogen receptor binding - 0.8074 80.74%
Androgen receptor binding - 0.8028 80.28%
Thyroid receptor binding - 0.6673 66.73%
Glucocorticoid receptor binding - 0.5498 54.98%
Aromatase binding - 0.8474 84.74%
PPAR gamma - 0.7652 76.52%
Honey bee toxicity - 0.9718 97.18%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity - 0.9565 95.65%

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 97.18% 96.09%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 93.15% 92.29%
CHEMBL2581 P07339 Cathepsin D 92.28% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.36% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.55% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 81.59% 90.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.38% 97.21%

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 25137912
LOTUS LTS0110867
wikiData Q27122518