Agelenin

目录号：SY-123392

Agelenin 是一种由 35 个氨基酸组成的多肽。Agelenin 可从阿格莱尼科蜘蛛 Agelena opulenta 中分离得到。Agelenin 与昆虫特异性钙通道抑制剂结构相似。

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(S)-Nicardipine

目录号：SY-123394

(S)-Nicardipine is the less active S enantiomer of Nicardipine. Nicardipine is a blocker of calcium channel(IC50 of 1 μM for blocking cardiac calcium channels).

¥638.00

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Verticilide

目录号：SY-123396

Verticilide是一种兰诺定受体(ryanodine)结合抑制剂，抑制ryanodine与兰诺定受体结合的IC50值为4.2 μM，对小鼠ryanodine受体的抑制作用较弱(IC50=53.9 μM)。

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ω-Conotoxin CnVIIA

目录号：SY-123398

ω-Conotoxin CnVIIA为含27个氨基酸的神经肽类毒素，具有N型钙电流阻滞活性。

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w-Conotoxin SVIB

目录号：SY-123400

ω-Conotoxin SVIB为从Conus venoms中分离得到的肽类毒素，具有抑制抽搐反应的能力，IC50值为37 nM。在小鼠体内，ω-Conotoxin SVIB可导致呼吸急迫，并在高浓度下致死。

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JTV-519 hemifumarate

目录号：SY-123402

JTV-519 hemifumarate,Antiarrhythmic and cardioprotective properties. is a Ca2+-dependent blocker of sarcoplasmic reticulum Ca2+-stimulated ATPase (SERCA) and a partial agonist of ryanodine receptors in striated muscle.

¥583.00

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L-Phenylalanine-D7

目录号：SY-123404

L-Phenylalanine-D7是L-Phenylalanine (T3377)的氘代物。L-Phenylalanine ( (S)-2-Amino-3-phenylpropionic acid)是从大肠杆菌分离的必需氨基酸，作为电压依赖性α2δ亚基Ca2+通道的拮抗剂，具有Ki值为980 nM。此外，它是NMDARs (KB573 μM)和非NMDARs的甘氨酸和谷氨酸结合位点的竞争性拮抗剂。L-Phenylalanine 被广泛用于食品香料和药品的生产。

¥5175.00

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Amlodipine aspartic acid impurity

目录号：SY-123406

Amlodipine aspartic acid is a calcium channel blocker compound that exhibits antihypertensive and antianginal properties. It is important to note that Amlodipine aspartic acid impurity is an impurity specific to this compound.

¥805.00

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L-Phenylalanine-13C9,15N,D8

目录号：SY-123408

L-Phenylalanine-13C9,15N,D8是一种带有13C，15N 标记和氘代标记的L-Phenylalanine (T3377)。L-Phenylalanine ( (S)-2-Amino-3-phenylpropionic acid)是从大肠杆菌中分离出来的必需氨基酸。它是一种电压依赖性α2δ亚基Ca2+通道拮抗剂，Ki值为980 nM。L-Phenylalanine 还是NMDARs (KB573 μM)和非NMDARs的甘氨酸和谷氨酸结合位点的竞争性拮抗剂，广泛用于食品香料和药品的生产。

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