2R-amino-4S-hydroxy-5-hexynoic acid

Details

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Internal ID 7a19a5b5-dd2a-4bb3-95ae-b06760ee4ee8
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > D-alpha-amino acids
IUPAC Name (2R,4S)-2-amino-4-hydroxyhex-5-ynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H9NO3/c1-2-4(8)3-5(7)6(9)10/h1,4-5,8H,3,7H2,(H,9,10)/t4-,5-/m1/s1
InChI Key HHGQBMHJPJMZRN-RFZPGFLSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H9NO3
Molecular Weight 143.14 g/mol
Exact Mass 143.058243149 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP -3.50
Atomic LogP (AlogP) -1.22
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2R-amino-4S-hydroxy-5-hexynoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9398 93.98%
Caco-2 - 0.9658 96.58%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4782 47.82%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.9560 95.60%
OATP1B3 inhibitior + 0.9218 92.18%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9244 92.44%
P-glycoprotein inhibitior - 0.9900 99.00%
P-glycoprotein substrate - 0.9756 97.56%
CYP3A4 substrate - 0.7606 76.06%
CYP2C9 substrate - 0.6009 60.09%
CYP2D6 substrate - 0.7646 76.46%
CYP3A4 inhibition - 0.9151 91.51%
CYP2C9 inhibition - 0.9421 94.21%
CYP2C19 inhibition - 0.9496 94.96%
CYP2D6 inhibition - 0.9565 95.65%
CYP1A2 inhibition - 0.9480 94.80%
CYP2C8 inhibition - 0.9657 96.57%
CYP inhibitory promiscuity - 0.9811 98.11%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.6919 69.19%
Eye corrosion - 0.9826 98.26%
Eye irritation - 0.5784 57.84%
Skin irritation - 0.7942 79.42%
Skin corrosion - 0.8998 89.98%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8864 88.64%
Micronuclear + 0.5574 55.74%
Hepatotoxicity + 0.6929 69.29%
skin sensitisation - 0.9099 90.99%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.7733 77.33%
Acute Oral Toxicity (c) III 0.6347 63.47%
Estrogen receptor binding - 0.9396 93.96%
Androgen receptor binding - 0.8322 83.22%
Thyroid receptor binding - 0.8023 80.23%
Glucocorticoid receptor binding - 0.8208 82.08%
Aromatase binding - 0.9388 93.88%
PPAR gamma - 0.7917 79.17%
Honey bee toxicity - 0.9139 91.39%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.9665 96.65%

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
CHEMBL221 P23219 Cyclooxygenase-1 95.26% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.16% 96.09%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 86.05% 92.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.02% 96.95%
CHEMBL2581 P07339 Cathepsin D 84.17% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.13% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.94% 91.11%

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 57380561
LOTUS LTS0203102
wikiData Q77381499