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About This Item
经验公式（希尔记法）:
C5H8O3
CAS号:
分子量:
116.12
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
98%
旋光性
[α]20/D −3° in methanol
折射率
n20/D 1.459 (lit.)
沸点
244-251 °C (lit.)
密度
1.2 g/mL at 25 °C (lit.)
官能团
carboxylic acid
ether
SMILES字符串
OC(=O)[C@@H]1CCCO1
InChI
1S/C5H8O3/c6-5(7)4-2-1-3-8-4/h4H,1-3H2,(H,6,7)/t4-/m0/s1
InChI key
UJJLJRQIPMGXEZ-BYPYZUCNSA-N
警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
230.0 °F - closed cup
闪点(°C)
110 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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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