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Merck
CN

06594

(S)-α-Allyl-proline hydrochloride

purum, ≥98.0% (TLC)

Synonym(s):

α-Allyl-D-proline hydrochloride, (S)-2-Allyl-2-pyrrolidinecarboxylic acid hydrochloride

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About This Item

Empirical Formula (Hill Notation):
C8H13NO2 · HCl
CAS Number:
129704-91-2
Molecular Weight:
191.66
NACRES:
NA.22
PubChem Substance ID:
329748251
UNSPSC Code:
12352200
MDL number:
MFCD06659238

Key Documents

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Product Name

(S)-α-Allyl-proline hydrochloride, purum, ≥98.0% (TLC)

Quality Level

100

InChI

1S/C8H13NO2.ClH/c1-2-4-8(7(10)11)5-3-6-9-8;/h2,9H,1,3-6H2,(H,10,11);1H/t8-;/m1./s1

SMILES string

Cl.OC(=O)[C@]1(CCCN1)CC=C

InChI key

DIYYEOOBZVTROL-DDWIOCJRSA-N

grade

purum

assay

≥98.0% (TLC)

form

powder or crystals

reaction suitability

reaction type: solution phase peptide synthesis

color

off-white to brown

mp

186-190 °C

application(s)

peptide synthesis

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Emily M Christensen et al.
The Journal of biological chemistry, 295(52), 18316-18327 (2020-10-29)
Pyrroline-5-carboxylate reductase 1 (PYCR1) catalyzes the biosynthetic half-reaction of the proline cycle by reducing Δ1-pyrroline-5-carboxylate (P5C) to proline through the oxidation of NAD(P)H. Many cancers alter their proline metabolism by up-regulating the proline cycle and proline biosynthesis, and knockdowns of

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Proline Derivatives and Analogs

Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.

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