beta-Ethynylserine

Details

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Internal ID 69abc23d-6b66-4179-a28a-dfd98d4bac17
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,3R)-2-amino-3-hydroxypent-4-ynoic acid
SMILES (Canonical) C#CC(C(C(=O)O)N)O
SMILES (Isomeric) C#C[C@H]([C@@H](C(=O)O)N)O
InChI InChI=1S/C5H7NO3/c1-2-3(7)4(6)5(8)9/h1,3-4,7H,6H2,(H,8,9)/t3-,4+/m1/s1
InChI Key RBWXRFBKVDBXEG-DMTCNVIQSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C5H7NO3
Molecular Weight 129.11 g/mol
Exact Mass 129.042593085 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP -3.90
Atomic LogP (AlogP) -1.61
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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3-Ethynylserine
64918-85-0
L-beta-ethynylserine
65207-64-9
9LA73F08EF
N721W38AZD
(2S,3R)-2-Amino-3-hydroxy-4-pentynoic acid
2-Amino-3-hydroxy-4-pentynoic acid, threo-
4-Pentynoic acid, 2-amino-3-hydroxy-, (R-(R*,S*))-
2(S),3(R)-2-Amino-3-hydroxypent-4-ynoic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of beta-Ethynylserine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9356 93.56%
Caco-2 - 0.9495 94.95%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.4860 48.60%
OATP2B1 inhibitior - 0.8623 86.23%
OATP1B1 inhibitior + 0.9738 97.38%
OATP1B3 inhibitior + 0.9586 95.86%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9399 93.99%
P-glycoprotein inhibitior - 0.9868 98.68%
P-glycoprotein substrate - 0.9909 99.09%
CYP3A4 substrate - 0.7676 76.76%
CYP2C9 substrate - 0.8021 80.21%
CYP2D6 substrate - 0.7778 77.78%
CYP3A4 inhibition - 0.7889 78.89%
CYP2C9 inhibition - 0.9002 90.02%
CYP2C19 inhibition - 0.8458 84.58%
CYP2D6 inhibition - 0.9362 93.62%
CYP1A2 inhibition - 0.8333 83.33%
CYP2C8 inhibition - 0.9842 98.42%
CYP inhibitory promiscuity - 0.9700 97.00%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6349 63.49%
Carcinogenicity (trinary) Non-required 0.6871 68.71%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.5061 50.61%
Skin irritation - 0.6873 68.73%
Skin corrosion - 0.9134 91.34%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8663 86.63%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.9521 95.21%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.6267 62.67%
Acute Oral Toxicity (c) III 0.6062 60.62%
Estrogen receptor binding - 0.9300 93.00%
Androgen receptor binding - 0.9207 92.07%
Thyroid receptor binding - 0.7571 75.71%
Glucocorticoid receptor binding - 0.8409 84.09%
Aromatase binding - 0.8943 89.43%
PPAR gamma - 0.7529 75.29%
Honey bee toxicity - 0.8688 86.88%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.9191 91.91%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.21% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.99% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 88.44% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.96% 99.17%

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 127838
LOTUS LTS0243763
wikiData Q82970415