Mouse Anti Human Pigment Epithelium-Derived Factor Clone PAT13D9AT 了解更多

Thymidylate Synthetase, Mouse Anti Human 了解更多

Lactate Dehydrogenase A, Mouse Anti Human 了解更多

Exenatide 了解更多

Exendin-4 Recombinant 了解更多

Inhibin Alpha Human Recombinant 了解更多

Adenosine Kinase Human Recombinant, Active 了解更多

Adenosine Kinase Human Recombinant 了解更多

Three Prime Repair Exonuclease 2 Human Recombinant 了解更多

Glutathione S-Transferase Alpha-1 Human Recombinant 了解更多

Beta Defensin-2 Mouse Recombinant 了解更多

Beta Defensin-2 Human Recombinant 了解更多

Interferon Alpha And Beta Receptor Mouse Recombinant 了解更多

Dengue Virus NS1 Subtype 2 Recombinant 了解更多

Dengue Virus Subtype 2 Recombinant, Insect Cells 了解更多

Hepatitis C Virus NS5B (2634-2752 a.a) Recombinant 了解更多

Human Papillomavirus 16 E6 Recombinant 了解更多

PF-06726304是一种有效且与SAM竞争的EZH2（Zeste Homolog 2的增强剂）赖氨酸甲基转移酶抑制剂。 了解更多

GR148672X是TGH抑制剂。 了解更多

NVP-2是一种有效的选择性ATP竞争性CDK9抑制剂，IC50值为0.5 nM。 了解更多

Cefamandole nafate is a pro-drug that is hydrolyzed by plasma esterases to produce cefamandole, second-generation cephalosporin antibiotic with bactericidal activity. Cefamandole nafate is used to study the effects of expression and inhibition of PBP 2A and other penicillin-binding proteins (PDPs) on bacterial cell wall mucopeptide synthesis. Cefamandole binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. 了解更多

Bentiromide is a peptide used as a screening test for exocrine pancreatic insufficiency and to monitor the adequacy of supplemental pancreatic therapy. It is given by mouth as a noninvasive test. The amount of 4-aminobenzoic acid and its metabolites excreted in the urine is taken as a measure of the chymotrypsin-secreting activity of the pancreas. 了解更多

Erythromycin estolate is a macrolide antibiotic, produced by Streptomyces erythreus. It is the lauryl sulfate salt of the propionic ester of erythromycin. This erythromycin salt acts primarily as a bacteriostatic agent. 了解更多

Cysteine is a thiol-containing non-essential amino acid that is oxidized to form CYSTINE. 了解更多

Glutarylcarnitine is the diagnostic metabolite for malonic aciduria and glutaric aciduria type I monitored in most tandem mass spectrometry newborn screening programmes. 了解更多

Kv3 modulator 4 is a Kv3.1 (pEC50=5.45) and Kv3.2 modulator extracted from patent WO2018020263A1, Cyclobutyl structure. 了解更多

Dicyclanil is an insect growth regulator compound with a similar chemical structure to cyromazine. 了解更多

Mutated EGFR-IN-2 (compound 91) is a mutant-selective EGFR inhibitor extracted from patent WO2017036263A1, which potently inhibits single-mutant EGFR (T790M) and double-mutant EGFR (including L858R/T790M (IC50=??1nM) and ex19del/T790M), and can suppress activity of single gain-of-function mutant EGFR (including L858R and ex19del) as well. Mutated EGFR-IN-2 shows anti-tumor antivity. 了解更多

NH2-Ph-C4-acid-NH2-Me (PROTAC Linker 31) is a PROTAC linker, which refers to the Alkyl-Chain composition. NH2-Ph-C4-acid-NH2-Me can be used in the synthesis of a series of PROTACs. 了解更多

Maribavir is an UL97 kinase inhibitor potentially for the treatment of cytomegalovirus (CMV) infection. The mechanism by which maribavir inhibits HCMV replication is by inhibition of an HCMV encoded protein kinase enzyme called UL97 or pUL97. 了解更多

Vc-seco-DUBA is a drug-linker conjugate for ADC with potent antitumor activity by using DUBA (DNA alkylating agent), linked via the ADC linker Vc-seco. 了解更多

Cy3 NHS (Cyanine3 NHS ester) is a water-soluble and yellow emitting fluorescent dye for labeling amino-groups in biomolecules. Used to label soluble proteins, peptides, and oligonucleotides/DNA. 了解更多

CNT2 inhibitor-1 is a potent concentrative nucleoside transporter 2 Inhibitor (CNT2), with an IC50 of 640 nM for hCNT2. 了解更多

(S)-Leucic acid is an amino acid metabolite. 了解更多

PF-06263276 (PF 6263276) is a potent and selective pan-JAK inhibitor, with IC50s of 2.2 nM, 23.1 nM, 59.9 nM and 29.7 nM for JAK1, JAK2, JAK3 and TYK2, respectively. 了解更多

Salermide is an inhibitor of Sirt1 and Sirt2; can cause strong cancer-specific apoptotic cell death. 了解更多

Petesicatib is a cathepsin S inhibitor, used in research of immune diseases. 了解更多

Fluzinamide is an effective antiepileptic. 了解更多

Propyl pyrazole triol (PPT) is an estrogen receptor alpha (ERα) agonist. 了解更多

6-(γ,γ-Dimethylallylamino)purine is a plant growth substance. 了解更多

Sutezolid (PNU-100480) is an oxazolidinone antimicrobial being developed for the treatment of tuberculosis. 了解更多

Tavilermide is a selective, partial agonist of TrkA, or a nerve growth factor (NGF) mimetic. 了解更多

Galidesivir hydrochloride (BCX 4430 hydrochloride) is a viral RNA-dependent RNA polymerase (RdRp) inhibitor; demonstrated broad-spectrum activity in multiple viruses and a favorable preliminary preclinical safety profile. 了解更多

D-3263 is an agonist of transient receptor potential melastatin member 8 (TRPM8) with potential antineoplastic activity. 了解更多

7-Chlorokynurenic acid sodium salt is a potent and selective antagonist of the glycine B coagonist site of the N-methyl-D-aspartate (NMDA) receptor (IC50=0.56 μM). 了解更多

(1R,2S)-VU0155041, Cis regioisomer of VU0155041, is a partial mGluR4 agonist with an EC50 of 2.35 μM. 了解更多

BTZ043 is an inhibitor of decaprenyl-phosphoribose-epimerase (DprE1), with MICs of of 2.3 nM and 9.2 nM for M. tuberculosis H37Rv and Mycobacterium smegmatis, respectively. 了解更多

CK-666 is a cell-permeable inhibitor of actin-related protein Arp2/3 complex, and binds to Arp2/3 complex, stabilizes the inactive state of the complex, blocking movement of the Arp2 and Arp3 subunits into the activated filament-like (short pitch) conformation. 了解更多

HG-9-91-01 is a potent and highly selective salt-inducible kinase (SIK) inhibitor with IC50s of 0.92 nM, 6.6 nM and 9.6 nM for SIK1, SIK2 and SIK3 respectively. 了解更多