delta1-Piperidine-6-carboxylic acid

Details

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Internal ID 387833de-109d-46fc-a6c9-1dfd4bb93e2d
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives
IUPAC Name 2,3,4,5-tetrahydropyridine-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H9NO2/c8-6(9)5-3-1-2-4-7-5/h4-5H,1-3H2,(H,8,9)
InChI Key CSDPVAKVEWETFG-UHFFFAOYSA-N
Popularity 0 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) 49.70 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.69
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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2,3,4,5-tetrahydropyridine-2-carboxylic acid
1-piperideine-6-carboxylic acid
2-Pyridinecarboxylic acid, 2,3,4,5-tetrahydro-
delta-1-Piperideine-6-carboxylate
2,3,4,5-tetrahydro-2-pyridinecarboxylic acid
delta-1-Piperidine-6-carboxylic acid
SCHEMBL574892
CHEBI:49015
DTXSID50952722
AKOS006376673
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of delta1-Piperidine-6-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9833 98.33%
Caco-2 - 0.7521 75.21%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7514 75.14%
OATP2B1 inhibitior - 0.8373 83.73%
OATP1B1 inhibitior + 0.9778 97.78%
OATP1B3 inhibitior + 0.9500 95.00%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.9503 95.03%
P-glycoprotein inhibitior - 0.9885 98.85%
P-glycoprotein substrate - 0.9825 98.25%
CYP3A4 substrate - 0.6908 69.08%
CYP2C9 substrate - 0.5973 59.73%
CYP2D6 substrate - 0.8526 85.26%
CYP3A4 inhibition - 0.9685 96.85%
CYP2C9 inhibition - 0.9656 96.56%
CYP2C19 inhibition - 0.9642 96.42%
CYP2D6 inhibition - 0.9472 94.72%
CYP1A2 inhibition - 0.9115 91.15%
CYP2C8 inhibition - 0.9441 94.41%
CYP inhibitory promiscuity - 0.9948 99.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.7222 72.22%
Eye corrosion - 0.7317 73.17%
Eye irritation + 0.9184 91.84%
Skin irritation + 0.6717 67.17%
Skin corrosion + 0.5776 57.76%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6889 68.89%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.5282 52.82%
skin sensitisation - 0.8243 82.43%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.5956 59.56%
Acute Oral Toxicity (c) III 0.4220 42.20%
Estrogen receptor binding - 0.9235 92.35%
Androgen receptor binding - 0.8385 83.85%
Thyroid receptor binding - 0.9138 91.38%
Glucocorticoid receptor binding - 0.9069 90.69%
Aromatase binding - 0.8637 86.37%
PPAR gamma - 0.6951 69.51%
Honey bee toxicity - 0.9551 95.51%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.9405 94.05%

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 88.81% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.67% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.23% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.58% 99.23%

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 165067
LOTUS LTS0028031
wikiData Q27104644