47532
Fmoc-D-Pro-OH
≥98.0%
Synonym(s):
Fmoc-D-proline
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About This Item
Empirical Formula (Hill Notation):
C20H19NO4
CAS Number:
Molecular Weight:
337.37
NACRES:
NA.26
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
MDL number:
Beilstein/REAXYS Number:
5856698
Quality Level
assay
≥98.0%
optical activity
[α]/D +31.0±3.0°, c = 1 in DMF
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
SMILES string
OC(=O)[C@H]1CCCN1C(=O)OCC2c3ccccc3-c4ccccc24
InChI
1S/C20H19NO4/c22-19(23)18-10-5-11-21(18)20(24)25-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2,(H,22,23)/t18-/m1/s1
InChI key
ZPGDWQNBZYOZTI-GOSISDBHSA-N
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Andreas Pech et al.
Nucleic acids research, 45(7), 3997-4005 (2017-02-06)
Biological evolution resulted in a homochiral world in which nucleic acids consist exclusively of d-nucleotides and proteins made by ribosomal translation of l-amino acids. From the perspective of synthetic biology, however, particularly anabolic enzymes that could build the mirror-image counterparts
Seon-Yeong Kwak et al.
Amino acids, 46(12), 2777-2785 (2014-09-15)
Caffeic acid (CA) is one of the antioxidants found in plants, which protects vascular cells against vascular injuries from oxidative stress. In our previous study, caffeoyl-prolyl-histidine amide (CA-L-Pro-L-His-NH2; CA-PH; a CA derivative) was synthesized, which exhibited a strong antioxidant activity
Global Trade Item Number
| SKU | GTIN |
|---|---|
| M5878-5G | 04061834060420 |
| M5878-10G | 04061834060413 |
| M5878-25G | 04061832392004 |
| 47532-5G | 04061832361666 |