A3903
1-氨基环丙烷羧酸
≥98% (TLC), powder, NMDA agonist
别名:
ACC, ACPC
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关于此项目
经验公式（希尔记法）:
C4H7NO2
化学文摘社编号:
分子量:
101.10
Beilstein:
2076413
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.32
产品名称
1-氨基环丙烷羧酸, ≥98% (TLC), powder
质量水平
方案
≥98% (TLC)
表单
powder
储存条件
(Keep container tightly closed in a dry and well-ventilated place.
Keep in a dry place.)
颜色
white
mp
229-231 °C (lit.)
溶解性
water: 49.00-51.00 mg/mL, clear, colorless
SMILES字符串
NC1(CC1)C(O)=O
InChI
1S/C4H7NO2/c5-4(1-2-4)3(6)7/h1-2,5H2,(H,6,7)
InChI key
PAJPWUMXBYXFCZ-UHFFFAOYSA-N
基因信息
human ... NARG2(79664)
mouse ... NARG2(93697)
rat ... LOC686240(686240), NARG2(691379)
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相关类别
一般描述
研究领域：细胞信号传导
1-氨基环丙烷羧酸（ACC）是一种非蛋白质氨基酸兼1-氨基环烷羧酸的成员。
1-氨基环丙烷羧酸（ACC）是一种非蛋白质氨基酸兼1-氨基环烷羧酸的成员。
应用
1-氨基环丙烷羧酸（ACC）已用作测定ACC脱氨酶活性的底物，以研究从蜈蚣草根、葫芦种子获得的内生隔离菌的促进植物生长特性。它还可用作乙烯合成前体，以研究高浓度乙烯对高粱褐中脉（BMR）突变体中侧根密度（LRD）的影响。
生化/生理作用
1-氨基环丙烷羧酸（ACC）是一种部分激动剂，作用于N-甲基-D-天冬氨酸盐（NMDA）受体甘氨酸调节位点上。ACC是植物激素乙烯的生物合成前体。此外，它在植物发育中起着至关重要的作用。ACC在大鼠和小鼠中表现出抗惊厥、抗焦虑、抗成瘾、神经保护和抗抑郁样作用。ACC不影响记忆或学习过程。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
农药列管产品
此项目有
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Plant, cell & environment, 43(6), 1558-1570 (2020-03-13)
Jasmonate synthesis and signalling are essential for plant defense upregulation upon herbivore or microbial attacks. Stress-induced accumulation of jasmonoyl-isoleucine (JA-Ile), the bioactive hormonal form triggering transcriptional changes, is dynamic and transient because of the existence of potent removal mechanisms. Two
Lorenzo Poncini et al.
PloS one, 12(10), e0185808-e0185808 (2017-10-04)
Plants interpret their immediate environment through perception of small molecules. Microbe-associated molecular patterns (MAMPs) such as flagellin and chitin are likely to be more abundant in the rhizosphere than plant-derived damage-associated molecular patterns (DAMPs). We investigated how the Arabidopsis thaliana
Joanna K Polko et al.
Frontiers in plant science, 10, 1602-1602 (2020-01-11)
1-Aminocyclopropane 1-carboxylic acid (ACC) is the direct precursor of the plant hormone ethylene. ACC is synthesized from S-adenosyl-L-methionine (SAM) by ACC synthases (ACSs) and subsequently oxidized to ethylene by ACC oxidases (ACOs). Exogenous ACC application has been used as a
Y A Kolesnikov et al.
Life sciences, 55(18), 1393-1398 (1994-01-01)
1-Aminocyclopropane carboxylic acid (ACPC), a partial agonist of the glycine site on the NMDA receptor, prevents tolerance to the mu opioid morphine and the delta ligand [D-Pen2,D-Pen5]enkephalin (DPDPE) when co-administered with the opioid. In contrast, ACPC does not significantly influence
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