2-Oxo-4-hydroxy-5-aminovalerate

Details

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Internal ID 19597323-2a21-4595-8421-a7b76095b67b
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Short-chain keto acids and derivatives
IUPAC Name (4R)-5-amino-4-hydroxy-2-oxopentanoic acid
SMILES (Canonical) C(C(CN)O)C(=O)C(=O)O
SMILES (Isomeric) C([C@H](CN)O)C(=O)C(=O)O
InChI InChI=1S/C5H9NO4/c6-2-3(7)1-4(8)5(9)10/h3,7H,1-2,6H2,(H,9,10)/t3-/m1/s1
InChI Key ICMJZHFYQVZYQN-GSVOUGTGSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C5H9NO4
Molecular Weight 147.13 g/mol
Exact Mass 147.05315777 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP -4.20
Atomic LogP (AlogP) -1.65
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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(4R)-5-amino-4-hydroxy-2-oxopentanoic acid
AC1L9A27
C05941
CHEBI:1241
SCHEMBL17285692
(4R)-5-amino-4-hydroxy-2-oxo-pentanoic acid
Q27105431

2D Structure

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2D Structure of 2-Oxo-4-hydroxy-5-aminovalerate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6781 67.81%
Caco-2 - 0.8994 89.94%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.4875 48.75%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.9512 95.12%
OATP1B3 inhibitior + 0.9266 92.66%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9673 96.73%
P-glycoprotein inhibitior - 0.9863 98.63%
P-glycoprotein substrate - 0.9707 97.07%
CYP3A4 substrate - 0.7518 75.18%
CYP2C9 substrate - 0.6173 61.73%
CYP2D6 substrate - 0.7370 73.70%
CYP3A4 inhibition - 0.8651 86.51%
CYP2C9 inhibition - 0.9572 95.72%
CYP2C19 inhibition - 0.9443 94.43%
CYP2D6 inhibition - 0.9560 95.60%
CYP1A2 inhibition - 0.9470 94.70%
CYP2C8 inhibition - 0.9861 98.61%
CYP inhibitory promiscuity - 0.9942 99.42%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7730 77.30%
Carcinogenicity (trinary) Non-required 0.6356 63.56%
Eye corrosion - 0.8475 84.75%
Eye irritation + 0.7057 70.57%
Skin irritation - 0.8004 80.04%
Skin corrosion - 0.9683 96.83%
Ames mutagenesis - 0.6854 68.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8619 86.19%
Micronuclear - 0.6500 65.00%
Hepatotoxicity + 0.5784 57.84%
skin sensitisation - 0.9472 94.72%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6688 66.88%
Acute Oral Toxicity (c) IV 0.5052 50.52%
Estrogen receptor binding - 0.9116 91.16%
Androgen receptor binding - 0.8099 80.99%
Thyroid receptor binding - 0.8015 80.15%
Glucocorticoid receptor binding - 0.7488 74.88%
Aromatase binding - 0.8333 83.33%
PPAR gamma - 0.6624 66.24%
Honey bee toxicity - 0.9511 95.11%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.9500 95.00%
Fish aquatic toxicity - 0.9709 97.09%

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 92.57% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.47% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.78% 99.17%
CHEMBL2581 P07339 Cathepsin D 82.41% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 81.91% 90.20%

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 440852
LOTUS LTS0134741
wikiData Q27105431