(3R)-3-hydroxy-D-aspartic acid

Details

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Internal ID 38e6f761-5ed2-4d4d-8235-c04a12c27ee3
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Aspartic acid and derivatives
IUPAC Name (2R,3R)-2-amino-3-hydroxybutanedioic acid
SMILES (Canonical) C(C(C(=O)O)O)(C(=O)O)N
SMILES (Isomeric) [C@@H]([C@H](C(=O)O)O)(C(=O)O)N
InChI InChI=1S/C4H7NO5/c5-1(3(7)8)2(6)4(9)10/h1-2,6H,5H2,(H,7,8)(H,9,10)/t1-,2-/m1/s1
InChI Key YYLQUHNPNCGKJQ-JCYAYHJZSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C4H7NO5
Molecular Weight 149.10 g/mol
Exact Mass 149.03242232 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP -4.40
Atomic LogP (AlogP) -2.16
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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(3R)-3-hydroxy-D-aspartic acid
(2R,3R)-2-amino-3-hydroxybutanedioic acid
DL-threo-beta-Hydroxyaspartic acid
4294-45-5
(2R,3R)-2-amino-3-hydroxysuccinic acid
(2R,3r)-2-amino-3-hydroxy-succinic acid
(R,R)-3-hydroxyaspartic acid
D-threo-3-hydroxyaspartic acid
threo-D-3-hydroxyaspartic acid
CHEBI:60897
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (3R)-3-hydroxy-D-aspartic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6232 62.32%
Caco-2 - 0.9889 98.89%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.4398 43.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9799 97.99%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9799 97.99%
P-glycoprotein inhibitior - 0.9810 98.10%
P-glycoprotein substrate - 0.9927 99.27%
CYP3A4 substrate - 0.7991 79.91%
CYP2C9 substrate - 0.6043 60.43%
CYP2D6 substrate - 0.7769 77.69%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9025 90.25%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition - 0.9886 98.86%
CYP inhibitory promiscuity - 0.9946 99.46%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7276 72.76%
Carcinogenicity (trinary) Non-required 0.7193 71.93%
Eye corrosion - 0.9963 99.63%
Eye irritation + 0.5928 59.28%
Skin irritation - 0.7488 74.88%
Skin corrosion - 0.9878 98.78%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8523 85.23%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.6925 69.25%
skin sensitisation - 0.9569 95.69%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6865 68.65%
Acute Oral Toxicity (c) III 0.5597 55.97%
Estrogen receptor binding - 0.8920 89.20%
Androgen receptor binding - 0.8753 87.53%
Thyroid receptor binding - 0.8011 80.11%
Glucocorticoid receptor binding - 0.7771 77.71%
Aromatase binding - 0.8709 87.09%
PPAR gamma - 0.7747 77.47%
Honey bee toxicity - 0.9336 93.36%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.9400 94.00%
Fish aquatic toxicity - 0.9060 90.60%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293237 P54132 Bloom syndrome protein 28.2 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4040 P28482 MAP kinase ERK2 94.52% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.90% 96.09%

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.
Astragalus sinicus

Cross-Links

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PubChem 11788378
NPASS NPC13243