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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T8555 | Neuraminidase-IN-1 | Novel NA Inhibitor,Compound Y-1 | Others , Influenza Virus |
Neuraminidase-IN-1 (Compound Y-1) is a novel neuraminidase inhibitor. | |||
T74350 | Neuropeptide Y Y1 receptor antagonist 1 | ||
Neuropeptide Y Y1 receptor antagonist 1 (compound 39), a fluorescent probe, serves as a powerful antagonist against the neuropeptide Y Y1 receptor (Y1R), exhibiting a Kᵢ value of 0.19 nM [1]. It should be stored in condi... | |||
T74459 | Y1R probe-1 | ||
Compound 39, also known as Y1R probe-1, is a high-affinity fluorescent probe targeting the Neuropeptide Y Y1 Receptor, with potential applications in cancer research [1]. | |||
T76355 | Neuropeptide Y (3-36) (porcine) | ||
Neuropeptide Y (3-36) (porcine) acts as an agonist for the Y2 subtype of the neuropeptide Y (NPY) receptor, effectively stimulating feeding behavior in rats. This compound exhibits high selectivity for the Y2 receptor co... | |||
T81470 | PI3K/mTOR Inhibitor-14 | PI3K | |
PI3K/mTOR Inhibitor-14 (compound Y-2) serves as a dual inhibitor of PI3K and mTOR, exhibiting IC50 values of 171.4 nM and 10.1 nM , respectively, and demonstrates antitumor activities [1]. | |||
T75912 | [Leu31,Pro34]-Neuropeptide Y(human,rat) TFA | ||
[Leu31,Pro34]-Neuropeptide Y(human,rat) TFA acts as a specific agonist for the neuropeptide Y Y1 receptor, while also activating receptors Y4 and Y5. This compound is known to elevate blood pressure in anesthetized rats ... | |||
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 is a useful organic compound for research related to life sciences. The catalog number is T125738 and the CAS number is 155408-18-7. | |||
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... | |||
T76357 | Neuropeptide Y (18-36) (porcine) | ||
Neuropeptide Y (18-36) (porcine) acts as a competitive antagonist of the neuropeptide Y (NPY) cardiac receptor, effectively blocking the attachment of I-NPY to cardiac ventricular membranes. Its action is concentration-d... | |||
T75900 | CART(55-102)(rat) TFA | ||
CART(55-102)(rat) TFA, a rat-derived satiety factor, exhibits potent appetite-suppressing properties. This compound is intricately linked to both leptin and neuropeptide Y, playing a crucial role in the regulation of hun... | |||
T76365 | CART (1-39), Human, Rat | ||
CART (1-39), Human, Rat is a neuropeptide comprising the first 39 residues of the CART peptide. This compound serves as a rat satiety factor, possessing significant appetite-suppressing effects, and demonstrates a close ... | |||
T75913 | [cPP1-7,NPY19-23,Ala31,Aib32,Gln34]-hPancreatic polypeptide TFA | ||
[cPP1-7,NPY19-23,Ala31,Aib32,Gln34]-hPancreatic Polypeptide is a potent, selective neuropeptide Y Y5 receptor agonist, demonstrating binding affinity with an IC50 of 0.24 nM for the hY5 receptor. This compound significan... | |||
T76356 | Neuropeptide Y (2-36) (porcine) | ||
Neuropeptide Y (2-36) (porcine) is a pig-sourced peptide closely resembling its rat and human counterparts with 97.14% homology. It acts as an agonist for rat neuropeptide receptors Y5, Y2, and Y1, demonstrating EC50 val... | |||
T75910 | GR231118 TFA | ||
GR231118 TFA, a neuropeptide Y C-terminus analogue, acts as a potent, competitive, and relatively selective antagonist at the human neuropeptide YY receptor, exhibiting a pKi of 10.4. It serves as a strong agonist at the... | |||
T79735 | DHFR-IN-9 | ||
DHFR-IN-9 (compound 8A), a dihydrofolate reductase (DHFR) inhibitor, impedes purine and thymidylate biosynthesis, pivotal in cell proliferation and growth. It demonstrates potency against methicillin-resistant Staphyloco... | |||
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 bac... | |||
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... |