Coelenterazine 400a is a bisdeoxy derivative of coelenterazine that displays an emission maximum of 395 nm following conversion by Renilla luciferase (Rluc).

Enzyme activity definition:One unit causes the formation of one micromole of hydrogen peroxide (half a micromole of quinoneimine dye) per minute under the conditions described below.

Fetuin, Fetal Bovine Serum is a glycoprotein from fetal bovine serum, which is often an important supplement to many serum-free media.

BYL719 (Alpelisib) is a selective PI3Kɑ inhibitor.

OSMI-1 is an O-GlcNAc transferase (OGT) small molecule inhibitor that does not significantly affect other glycosyltransferases

Ampicillin is a broad-spectrum beta-lactam antibiotic against a variety of gram-positive and gram-negative bacteria.

ARV471 is an orally bioavailable estrogen receptor-targeting (ER-targeting) PROTAC for the treatment of patients with locally advanced or metastatic ER+/HER2- breast cancer.

Danshensu, an active ingredient of Salvia miltiorrhiza, shows wide cardiovascular benefit by activating Nrf2 signaling pathway.

Piceatannol (3,3′,4,5′-trans-trihydroxystilbene) is a naturally occurring hydroxylated analogue of resveratrol. 

DB1976 hydrochloride is a selenophene analog of DB270 and a potent and cell-permeable fully efficacious transcription factor PU.1 inhibitor. 

Vitexin is an active components of many traditional Chinese medicines, and were found in various medicinal plants. 

Decoyinine is a selective inhibitor of GMP synthetase (GMPS).

Gracillin, as a natural steroidal saponin component of D. quinqueloba, has antitumour, antimicrobial, antioxidant, pro‐apoptotic and anti‐inflammatory properties.

PF-07104091 hydrate is a potent and selective CDK2/cyclin E1 and GSK3β inhibitor, with Kis of 1.16 and 537.81 nM, respectively.

Calycosin (CA, 7, 3-dihydroxy-4-methoxy isoflavone, C16H12O5) is one of the flavonoids extracted from astragalus root, also known as the typical phytoestrogens.

PLGA(poly (lactic-co-glycolic acid)) is made by random polymerization of two monomers: lactic acid and glycolic acid.

Methylophiopogonanone A (MOA), an abundantly bioactive homoisoflavonoid isolated from the herbal medicine Ophiopogonis Radix, has been considered as the key chemical index for the quality control of Ophiopogonis Radix related herbal formulations.

Sulfo-NHS-SS-biotin is an amine-reactive biotinylating reagent.

Baohuoside I, a flavonoid isolated from Epimedium koreanum Nakai, acts as an inhibitor of CXCR4, downregulates CXCR4 expression, induces apoptosis and shows anti-tumor activity.

SRI 37892 is a small molecule compound inhibitor of Frizzled protein 7 (Fzd7) with inhibitory activity against cancer cell proliferation (IC502μM).

Tarloxotinib bromide is an irreversible EGFR/HER2 inhibitor.

GP(33-41), a 9-aa-long peptide, is the optimal sequence of the GP1 epitope of lymphocytic choriomeningitis virus, and can upregulate H-2Db molecules at the RMA-S (Db Kb) cell surface with a SC50 of 344 nM.

Amyloid Beta-Peptide (12-28) (human) is a peptide fragment of amyloid beta protein (1-42) (Aβ (1-42)).

DFO (9H-1,8-Diazafluoren-9-one) is a fluorescent dye that reacts with amino acids to form highly fluorescent derivatives (excitation wavelength ~470 nm;Emission wavelength ~570 nm) is used to detect potential fingerprints on paper, and has a very high sensitivity and is widely used in sweat fingerprint identification.

GDC-0068 (RG7440, Ipatasertib) is a novel highly selective ATP-competitive pan-Akt inhibitor that inhibits all three isoforms of Akt1, Akt2, and Akt3 at an IC50 of 5,18,8 nM, respectively.

Ecdysone (α-ecdysone) is a steroidal molting hormone that exists in insects and plants and  activates  mineralocorticoid receptor (MR), leading to glomerular diseases.

High affinity, selective KCa2.2 blocker

Belumosudil mesylate (KD025 mesylate) is a selective inhibitor of ROCK2 with IC₅₀ of 105 nM and 24 µM for ROCK2 and ROCK1, respectively. 

KATP channel blocker; HMR 1098 acts by inactivating the ATP-sensitive potassium channels (KATP) responsible for potassium efflux. HMR 1098 is an inhibitor of Kir6.2/SUR1-composed K(ATP) channels

A cyclic depsipeptide and an inhibitor of Gα_q, Gα₁₁, and Gα₁₄