Weight | 129.159 g/mol |
---|---|
Formula | C6H11NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
l-Pipecolic acid (3105-95-1)
pipecolic acid · pipecolic acid, (R)-isomer · pipecolic acid, (+,-)-isomer
Score:
#1430 in Biochemistry
,
#3397 in Biology
,
#4242 in Chemistry
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- Cerebro-hepato-renal syndrome of Zellweger. A report of eight cases with comments upon the incidence, the liver lesion, and a fault in pipecolic acid metabolism. (The Journal of Pediatrics, 1975)
- Pipecolic acid, an endogenous mediator of defense amplification and priming, is a critical regulator of inducible plant immunity. (The Plant Cell, 2012)
- Enzymatic synthesis of L-pipecolic acid and L-proline. (Journal of Biological Chemistry, 1957)
- Pipecolic acid pathway: The major lysine metabolic route in the rat brain (Biochemical and Biophysical Research Communications, 1976)
- Asymmetric synthesis of pipecolic acid derivatives using the aza-Diels-Alder reaction (Tetrahedron-asymmetry, 1991)
- Lysine metabolism in the rat brain: the pipecolic acid-forming pathway. (Journal of Neurochemistry, 1978)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - pipecolic acid
- pipecolic acid, (R)-isomer
- pipecolic acid, (+,-)-isomer
- pipecolic acid, (S)-isomer
- pipecolic acid hydrochloride, (+-)-isomer
- pipecolic acid, ion (1-)
- pipecolic acid, ion(1-), (S)-isomer
- pipecolic acid, monopotassium salt
- homopipecolic acid
- pipecolic acid, 14C-labeled cpd, (+,-)-isomer
- pipecolic acid, ion(1-), (+,-)-isomer
-
SMILESC1CCNC(C1)C(=O)O
-
InChIKeyHXEACLLIILLPRG-UHFFFAOYSA-N
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