Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
TN2116 | Pteropodine
钩藤碱 C
|
5629-60-7 | 98% |
|
Pteropodine acts as a positive modulator of muscarinic M(1) and 5-HT(2) receptors. Pteropodine shows antigenotoxic, antioxidant and lymphocyte induction effects,... | ||||
T16447 | β-Amino Acid Imagabalin Hydrochloride
化合物 T16447
|
610300-00-0 | 98% |
|
β-Amino Acid Imagabalin Hydrochloride is the voltage-dependent calcium channel ligand for the α2δ subunit. | ||||
TN4819 | (-)-Praeruptorin A
化合物 TN4819
|
14017-71-1 | 98% |
|
(-)-Praeruptorin A has anti-inflammatory, anti-contractile and anti-hyperplasia activities, it exerts distinct relaxant effects on isolated rat aorta rings depen... | ||||
T13250 | UK51656
化合物 T13250
|
88150-59-8 | 98% |
|
UK51656 is an antagonist of calcium (IC50: 4 nM). | ||||
TN2287 | Turkesterone
土克甾酮
|
41451-87-0 | 98% |
|
Turkesterone is a phytoecdysteroid possessing an 11alpha-hydroxyl group, also is an analogue of the insect steroid hormone 20-hydroxyecdysone. It has immunomodul... | ||||
TL0014 | Pinusolide
化合物 TL0014
|
31685-80-0 | 98% |
|
Pinusolide is a platelet activating factor ( PAF) antagonist, it may prove of therapeutic value in the treatment of hypotension, it has antileukemic potential, a... | ||||
TN2918 | 3-Acetoxy-8(17),13E-labdadien-15-oic acid
化合物 TN2918
|
63399-37-1 | 98% |
|
ent-3-Acetoxy-labda-8(17),13-dien-15-oic acid have vasorelaxant and hypotensive actions, the mechanisms underlying the cardiovascular actions of the labdane invo... | ||||
TN5234 | Vindorosine
化合物 TN5234
|
5231-60-7 | 98% |
|
Vindorosine has blood vessel relaxation effect, possible underlying mechanisms involving the inhibition of Ca(2+) entry via L-type Ca(2+) channels in vascular sm... | ||||
TN1588 | Dihydroisotanshinone I
二氢异丹参酮I
|
20958-18-3 | 98% |
|
Dihydroisotanshinone I has protective action against menadione-induced hepatotoxicity, attributed to its antioxidant properties including the free radical scaven... | ||||
T39195 | YM-244769 dihydrochloride
化合物YM-244769 dihydrochloride
|
1780390-65-9 | 98% |
|
YM-244769 dihydrochloride 是一种有效的 Na+/Ca2+ exchange 3 (NCX3) 抑制剂,IC50 为 18 nM。 YM-244769 dihydrochloride 对神经元和肾脏具有有效的保护作用。 | ||||
TN4303 | Isokaempferide
化合物 TN4303
|
1592-70-7 | 98% |
|
Isokaempferide shows hepatoprotective, antiproliferative, and anti-inflammatory effects, the anti-inflammatory effects can be explained, at least in part, by red... | ||||
T9888 | YM-244769
化合物YM-244769
|
838819-70-8 | 98% |
|
YM-244769 (3-Pyridinecarboxamide, N-[(3-aminophenyl)methyl]-6-[4-[(3-fluorophenyl)methoxy]phenoxy]-) 是一种有效的 Na+/Ca2+ exchange 3 (NCX3) 抑制剂,IC50 为 18 nM。 YM-24476... | ||||
TMA0805 | Lupanine
化合物 TMA0805
|
550-90-3 | 98% |
|
Lupanine has a weak sedative effect on the central nervous system, interaction with specific drugs used for treatment of the CNS and for analgesic activity. Lupa... | ||||
TN3406 | Ambocin
化合物Ambocin
|
108044-05-9 | 98% |
|
Ambocin 是葛根的天然产物。 Ambocin 以浓度依赖性方式阻断通过 CaV1.2 通道 (IBa1.2) 的 Ba2+ 电流并增加 IKCa1.1。 | ||||
TN5279 | Zeorin
化合物 TN5279
|
22570-53-2 | 98% |
|
Zeorin shows strong inhibition activity against bacteria and fungi. It markedly exhibits inhibitory activity on histamine release from mast cell induced by DNP24... | ||||
T12108 | MRS1845
化合物 T12108
|
544478-19-5 | 98% |
|
MRS1845 is a selective inhibitor of store-operated calcium (SOC) channel (IC50 of 1.7 μM). | ||||
T38047 | Maresin 1
化合物 Maresin 1
|
1268720-28-0 | 98% |
|
Maresin 1 是由巨噬细胞 (MΦ) 生物合成的小分子化合物,具有显著的抗炎活性,可通过抑制中性粒细胞粘附和降低促炎细胞因子水平来减轻LPS诱导的小鼠肺损伤,可以刺激胞内 Ca2+ 产生和分泌。 | ||||
T12993 | SQ-31765
化合物 T12993
|
138383-07-0 | 98% |
|
SQ-31765 is a blocker of benzazepine calcium channel. | ||||
T3229 | Cytochalasin D
细胞松弛素D
|
22144-77-0 | 98% |
|
Cytochalasin D is an actin inhibitor, the removal of actin stress fibers is crucial for the chondrogenic differentiation. It may be an inhibitor of some fertiliz... | ||||
T12153 | N-type calcium channel blocker-1
化合物 T12153
|
241499-17-2 | 98% |
|
N-type calcium channel blocker-1 is an orally active analgesic agent,shows high affinity to functionally block N-type calcium channels. |