Sulfo - Cyanine 3 NHS, a water - soluble and amine - reactive compound, can efficiently label proteins and polypeptides in pure aqueous solutions without the need for organic co - solvents. This makes it an ideal option for proteins with low solubility and those prone to denaturation. Moreover, the Sulfo - Cyanine 3 NHS ester can serve as a substitute for Cy3, Alexa Fluor 546, and DyLight 549, offering a practical alternative in various experimental and research settings.

6-JOE NHS is an amine-reactive fluorescent probe and is suitable for postsynthetic labeling of amino-modified oligonucleotides

6 - NED can be employed in multiple applications, including fragment analysis, gene expression studies, genotyping, and PCR techniques. 6 - NED NHS is a highly stable fluorescent probe. It has seen widespread use in the field of labeling amino - modified oligonucleotides, contributing to more accurate and efficient research efforts in relevant biological and genetic studies.

6-HEX NHS is the amine-reactive succinimidyl ester of 6-HEX acid. It has found extensive applications in nucleic acid sequencing and related research fields. This NHS ester belongs to a class of amine-reactive dyes. It is utilized for labeling amine groups in various target molecules, such as proteins, peptides, and amino-modified oligomers.

5-FAM SE is a single isomer, it is one of the most popular green fluorescent reagents used for labeling peptides, proteins and nucleotides.

Fluorescein isothiocyanate(FITC) is a derivative of fluorescein used in wide-ranging applications including flow cytometry.

WEE1-IN-10 (compound 77) is a Wee1 kinase inhibitor. WEE1-IN-10 shows inhibitory activity on LOVO cell growth, with an IC50 of 0.524 μM. WEE1-IN-10 can be used for the research of diseases caused by abnormal activity of Wee1.

DL-5-Indolylmethylhydantoin can be used as a substrate for the enzymatic production of L-tryptophan in some specific bacteria.

Wnt pathway activator 2 (compound 2) is a potent Wnt activator with an EC50 of 13 nM.

JZL184 is a strong and selective inhibitor of Monoglyceride Lipase

YO-01027 (Dibenzazepine, DBZ) is a dipeptidic g-secretase inhibitor with IC50 of 2.6 and 2.9 nM for APPL and Notch, respectively.

8-Hydroxy-DPAT hydrobromide (8-OH-DPAT hydrobromide) is a potent and selective 5-HT1A agonist with a pIC50 of 8.19. 8-Hydroxy-DPAT hydrobromide has selectivity of almost 1000 fold for a subtype of the 5-HT1 binding site.

CeMMEC13 is a potent inhibitor of TAF1 (2) bromodomain, with an IC50 of 2.1 μM.

E-64c is a synthetic analog of E-64, a potent and irreversible cysteine protease inhibitor isolated from Aspergillus japonicus.

UNC-0224 is a potent inhibitor of G9a histone lysine methyltransferase (IC50 = 15 nM).

KML29 is an O-hexafluoroisopropyl carbamate analog of JZL 184 that potently and selectively inhibits MAGL (IC50s = 15, 43, and 5.9 nM in mouse, rat, and human brain proteomes, respectively) over FAAH (IC50s >50 μM).

OPC-21268 is a vasopressin 1 receptor antagonist potentially for the treatment of heart failure and hypertension.

NS-398 is a selective inhibitor of cyclooxygenase-2 (COX-2).

Bay K-8644 is a potent L-type calcium channels (LTCCs) activator with EC50 of 17.3 nM, has positive inotropic, vasoconstrictive and behavioral effects in vivo.

YU238259 is a novel inhibitor of homology-dependent DNA repair(HDR), but does not inhibit non-homologous end-joining (NHEJ), in cell-based GFP reporter assays.

C646 is an inhibitor for histone acetyltransferase, and inhibits p300 with a Ki of 400 nM. Preferentially selective for p300 versus other acetyltransferases.

Dp44mT is a potent iron chelator, which shows selective antitumor activity.

Azoramide is a small-molecule modulator of the unfolded protein response with antidiabetic activity.

LY2603618(IC-83) is a potent and selective small molecule inhibitor of Chk1 protein kinase activity in vitro (IC50=7 nM) and the first selective Chk1 inhibitor to enter clinical cancer trials.