Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8555 |
Neuraminidase-IN-1
Novel NA Inhibitor,Compound Y-1 |
Others; Influenza Virus | Microbiology/Virology; Others |
Neuraminidase-IN-1 (Compound Y-1) 是一种神经氨酸酶抑制剂,其IC50值为 0.21 μM,具有抗H1N1流感病毒的活性。 | |||
T74350 |
Neuropeptide Y Y1 receptor antagonist 1
|
||
Neuropeptide Y Y1 receptor antagonist 1 (化合物 39),一种荧光探针,是神经肽 Y Y1受体 (Y1R) 的拮抗剂,Ki 值为 0.19 nM。储存方式:避光。 | |||
T76355 |
Neuropeptide Y (3-36) (porcine)
|
||
Neuropeptide Y (3-36) (porcine) 是一种针对 Y2 亚型的 NPY 受体的激动剂,同时也通过一种尚未明确的受体来调控大鼠的摄食行为。 | |||
T74459 | Y1R probe-1 | ||
Y1R probe-1 (Compound 39) 是一种针对神经肽Y Y1受体的高亲和力荧光探针,具有潜在应用于癌症疾病研究。 | |||
T75912 |
[Leu31,Pro34]-Neuropeptide Y(human,rat) TFA
|
||
[Leu31,Pro34]-Neuropeptide Y(human,rat) TFA 是一种针对神经肽 YY1受体的特定激动剂,并亦能够激活Y4和Y5受体。该化合物能提高麻醉大鼠的血压并增加食物摄入。 | |||
T81470 |
PI3K/mTOR Inhibitor-14
|
PI3K | PI3K/Akt/mTOR signaling |
PI3K/mTOR Inhibitor-14(化合物 Y-2)是一种针对PI3K和mTOR的双重抑制剂,其IC50值分别为171.4 nM 和10.1 nM ,具备抗肿瘤活性。 | |||
T40211 |
eIF4E-IN-1
eIF4E-IN-1 |
||
eIF4E-IN-1 (WO2021003194A1, compound Y), is a highly effective inhibitor of eIF4E, a key protein involved in immunosuppression. By targeting immune checkpoint proteins such as PD-1, PD-L1, LAG3, TIM3, and IDO, eIF4E-IN-1 functions to disrupt immune suppression and promote immune release in specific diseases such as cancer and infectious diseases. | |||
T76357 |
Neuropeptide Y (18-36) (porcine)
|
||
Neuropeptide Y (18-36) (porcine) 是一种与Neuropeptide Y(NPY)心脏受体进行竞争性拮抗的化合物。该化合物通过浓度依赖的方式,抑制I-NPY与心室膜的结合,具有IC50值158 nM和Ki值140 nM。Neuropeptide Y (18-36) (porcine) 主要用于充血性心力衰竭的研究。 | |||
T125738 |
2-[(1R,2R)-3-oxo-2-[(2Z)-5-(sulfooxy)pent-2-en-1-y
|
||
2-[(1R,2R)-3-oxo-2-[(2Z)-5-(sulfooxy)pent-2-en-1-y 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T125738,CAS号为 155408-18-7。 | |||
T75900 |
CART(55-102)(rat) TFA
|
||
CART(55-102)(rat) TFA,一种鼠源性饱腹感因子,具强烈抑制食欲作用,与瘦素及神经肽 Y 有密切关联,能诱导焦虑及压力相关行为。 | |||
T75913 |
[cPP1-7,NPY19-23,Ala31,Aib32,Gln34]-hPancreatic polypeptide TFA
|
||
[cPP1-7,NPY19-23,Ala31,Aib32,Gln34]-hPancreatic Polypeptide 为高效且选择性的神经肽 YY5 受体激动剂,其与 hY5 受体的结合 IC50 值为 0.24 nM,已知可促进饮食摄入。 | |||
T76365 |
CART (1-39), Human, Rat
|
||
CART (1-39), Human, Rat, 是一种由其1至39个残基构成的神经肽, 具有明显的减少食欲作用, 被认为是鼠类的饱腹因子, 并与瘦素及神经肽Y有着紧密的联系。它能有效抑制正常及饥饿状态下的摄食行为, 同时也能引发焦虑与压力相关的反应。 | |||
T76356 |
Neuropeptide Y (2-36) (porcine)
|
||
Neuropeptide Y (2-36) (porcine) 是一种具有 97.14% 与大鼠/人类同源性的猪源性神经肽。作为一种大鼠神经肽受体激动剂,其对Y5、Y2和Y1受体的EC50值为1.2, 1.6 和 3.4 nM,能显著增加食物摄入量,适用于肥胖和饮食失调研究。 | |||
T75910 |
GR231118 TFA
|
||
GR231118是神经肽Y的C末端类似物,作为人神经肽YY受体的高竞争性和相对选择性的拮抗剂(pKi=10.4),并对人类神经肽Y4受体显示出拮抗效果(pEC50=8.6;pKi=9.6),同时是对人及大鼠神经肽YY2与Y5受体的弱激动剂。此外,GR231118对小鼠神经肽YY6受体具有较高亲和力(pKi=8.8)。 | |||
T79735 |
DHFR-IN-9
|
||
DHFR-IN-9(化合物8A)是一种二氢叶酸还原酶(DHFR)抑制剂,通过干扰细胞内嘌呤和胸苷酸的生物合成而影响细胞生长和增殖。该化合物对抗耐甲氧西林金黄色葡萄球菌(MRSA)ATCC 43300展现出显著的抑制效果(IC50=0.25 μg/mL),并在全身及大腿感染的小鼠模型中显示出抗感染能力(剂量:2.5 mg/kg,5 mg/kg;ip)。此外,DHFR-IN-9在乳腺癌小鼠模型中展示了超过紫杉醇(Y-B0015)的抗癌活性(剂量:2.5 mg/kg;ip;每3天1次)。 | |||
T37674 |
Aspyrone
|
||
Aspyrone is a polyketide fungal metabolite that has been found inAspergillusand has diverse biological activities.1,2It is active against a panel of 13 fungi when used at a concentration of 20 μg/ml and a panel of 21 bacteria in a disc assay when used at a concentration of 100 μg per disc.1Aspyrone (10-1,000 mg/L) is nematocidal againstP. penetrans.2 1.Torres, M., Balcells, M., Sala, N., et al.Bactericidal and fungicidal activity of Aspergillus ochraceus metabolites and some derivativesPestic. S... | |||
T35742 |
IKD-8344
|
||
IKD-8344 is a macrocyclic dilactone originally isolated from an actinomycete species and has diverse biological activities, including anticancer, antimicrobial, and anthelmintic properties.1,2,3 It is cytotoxic to L5178Y murine leukemia cells (IC50 = 0.54 ng/ml).1 IKD-8344 inhibits growth of the mycelial form of C. albicans (MIC = 6.25 μg/ml) and potentiates the activity of polymyxin B against the multidrug-resistant pathogenic bacterium B. cenocepacia.2,3 It is active against T. spiralis in vit... |