Homopropargylglycine

Details

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Internal ID 1ef704f3-eeb3-4e74-b283-504a2a16a7e0
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name 2-aminohex-5-ynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H9NO2/c1-2-3-4-5(7)6(8)9/h1,5H,3-4,7H2,(H,8,9)
InChI Key SCGJGNWMYSYORS-UHFFFAOYSA-N
Popularity 80 references in papers

Physical and Chemical Properties

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Molecular Formula C6H9NO2
Molecular Weight 127.14 g/mol
Exact Mass 127.063328530 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP -2.40
Atomic LogP (AlogP) -0.19
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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Homopropargylglycine
215160-72-8
2-aminohex-5-ynoic acid
H-Hpg-OH
2-amino-5-hexynoicacid
SCHEMBL869479
AKOS000193191
HY-W259668
MS-22767
CS-0433729
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Homopropargylglycine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9722 97.22%
Caco-2 - 0.8849 88.49%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.5666 56.66%
OATP2B1 inhibitior - 0.8425 84.25%
OATP1B1 inhibitior + 0.9738 97.38%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9494 94.94%
P-glycoprotein inhibitior - 0.9925 99.25%
P-glycoprotein substrate - 0.9849 98.49%
CYP3A4 substrate - 0.7407 74.07%
CYP2C9 substrate + 0.5914 59.14%
CYP2D6 substrate - 0.7772 77.72%
CYP3A4 inhibition - 0.9138 91.38%
CYP2C9 inhibition - 0.9404 94.04%
CYP2C19 inhibition - 0.9664 96.64%
CYP2D6 inhibition - 0.9718 97.18%
CYP1A2 inhibition - 0.9137 91.37%
CYP2C8 inhibition - 0.9846 98.46%
CYP inhibitory promiscuity - 0.9770 97.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6333 63.33%
Eye corrosion - 0.9732 97.32%
Eye irritation + 0.6831 68.31%
Skin irritation - 0.6938 69.38%
Skin corrosion + 0.9259 92.59%
Ames mutagenesis - 0.6978 69.78%
Human Ether-a-go-go-Related Gene inhibition - 0.8854 88.54%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.6895 68.95%
skin sensitisation - 0.9046 90.46%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7578 75.78%
Acute Oral Toxicity (c) III 0.4585 45.85%
Estrogen receptor binding - 0.9476 94.76%
Androgen receptor binding - 0.8685 86.85%
Thyroid receptor binding - 0.8678 86.78%
Glucocorticoid receptor binding - 0.8869 88.69%
Aromatase binding - 0.9529 95.29%
PPAR gamma - 0.7566 75.66%
Honey bee toxicity - 0.9598 95.98%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.9258 92.58%

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 92.19% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.62% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 91.48% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.99% 99.17%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 84.17% 92.29%
CHEMBL236 P41143 Delta opioid receptor 84.10% 99.35%
CHEMBL274 P51681 C-C chemokine receptor type 5 83.51% 98.77%
CHEMBL230 P35354 Cyclooxygenase-2 81.31% 89.63%

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.
There are no matching plants.

Cross-Links

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PubChem 15837543
LOTUS LTS0136344
wikiData Q105250100