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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T71832 | CTX-0124143 | Histone Acetyltransferase | |
CTX-0124143 is a histone acetyltransferase inhibitor with an IC50 value of 1.0 μM for KAT6A.CTX-0124143 can be used to study cellular senescence. | |||
T2042 | CTX-0294885 | Others | |
CTX-0294885, a novel bisanilino pyrimidine, exhibits inhibitory activity against a broad range of kinases in vitro and is further developed into a Sepharose-supported kinase capture reagent. | |||
TP1289 | Cardiotoxin Analog (CTX) IV (6-12) TFA | Cardiotoxin Analog (CTX) IV (6-12) (TFA)(115722-23-1,FREE) | Others |
Cardiotoxin Analog IV (6-12) TFA, a partial peptide of Cardiotoxin Analog IV, is derived from the venom of the Taiwan Cobra, showcasing the unique properties of snake venom cardiotoxin[1]. | |||
T3715 | Acebilustat | CTX-4430 | Aminopeptidase , LTR |
Acebilustat (CTX-4430) (ZK322) is an effective and specific leukotriene B4 hydrolase inhibitor. | |||
T9167 | PF-9363 | CTX-3648 | Histone Acetyltransferase |
PF-9363 (CTX-3648) is a potent and high selective KAT6A/KAT6B inhibitor. PF-9363 can be used for the research of cancer. | |||
TP1455 | Cardiotoxin Analog (CTX) IV (6-12) | Cardiotoxin Analog (CTX) IV 6-12 | |
Cardiotoxin Analog (CTX) IV (6-12) is a part peptide of Cardiotoxin Analog (CTX) IV. Cardiotoxin analogues IV isolated from the venom of Taiwan Cobra. | |||
T19251 | CTX-0294885 hydrochloride (1439934-41-4 free base) | CTX-0294885 hydrochloride | Others |
CTX-0294885 hydrochloride is an agarose-supported kinase capture reagent. | |||
T82664 | CTX-2026 | ||
CTX-2026, a fully human antibody, targets and binds to CD277, demonstrating an anti-tumor effect in ovarian tumor models, and is utilized in cancer research [1]. | |||
T62049 | CTX-712 | ||
CTX-712 is a potent inhibitor of cdc2-like kinase ( CLK ). CTX-712 inhibits inhibits cancer survival and cancer cell growth. | |||
T76734 | CTX-471 | ||
CTX-471, a fully human monoclonal antibody targeting CD137, exhibits binding affinity for CD137 across multiple species, including humans, cynomolgus macaques, and mice, with dissociation constant (Kd) values of 50 nM, 6... | |||
T72214 | CTX-0294885 hydrochloride | ||
CTX-0294885 hydrochloride is a broad-spectrum kinase inhibitor capable of capturing 235 kinases from MDA-MB-231 cells, including all members of the AKT family. This compound serves as a potent tool for analyzing kinome s... | |||
T23707 | Alpha-Conotoxin imi | alpha-Ctx-imi | |
alpha-Conotoxin imi is a nicotinic acetylcholine receptor ligand. | |||
T15016 | CTX1 | p53 | |
CTX1 is a small molecule activator of p53. | |||
T4584 | BMS-813160 | BMS 813160 | CCR |
BMS-813160 is the first dual CCR2/CCR5 antagonist to enter Clinical development for cardiovascular. | |||
T60050 | ANT3310 | Antibacterial | |
ANT3310 is an inhibitor of broad-spectrum covalent Serine β-Lactamase with IC50s ranging from 1 nM to 175 nM for AmpC, CTX-M-15, TEM-1, OXA-48, OXA-23, and KPC-2. ANT3310 can be used in studies about bacterial infection. | |||
T38941 | FPI-1523 sodium | Endogenous Metabolite , Antibacterial | |
FPI-1523 sodium, a derivative of avibactam, is a potent β-lactamase inhibitor with K d s of 4 nM and 34 nM for CTX-M-15 and OXA-48, respectively.FPI-1523 sodium inhibited PBP2 with an IC 50 of 3.2 μM.FPI-1523 sodium has ... | |||
T10422 | Avibactam free acid | NXL-104 free acid | Antibacterial |
Avibactam (NXL-104) free acid is a covalent and reversible inhibitor of non-β-lactam β-lactamase (IC50s: 8 nM and 5 nM for β-lactamase TEM-1 and CTX-M-15). | |||
T10713 | CCR4 antagonist 2 | Calcium Channel | |
CCR4 antagonist 2 (Compound 31) is a novel potent, orally bioavailable small molecule antagonists of CC chemokine receptor 4 (CCR4) that inhibits Treg trafficking into the Tumor Microenvironment without suppressing the n... | |||
T39661 | CCR4 antagonist 3 | CCR4 antagonist 3 | |
CCR4 antagonist 3 is an orally active, potent and selective CCR4 antagonist. CCR4 antagonist 3, featuring a novel piperidinyl-azetidine motif, has IC 50 s of 22 nM and 50 nM in the calcium flux and CTX assay. CCR4 antago... | |||
T39662 | CCR4 antagonist 3 hydrochloride | ||
CCR4 antagonist 3 hydrochloride is an orally active, potent and selective CCR4 antagonist. CCR4 antagonist 3, featuring a novel piperidinyl-azetidine motif, has IC 50 s of 22 nM and 50 nM in the calcium flux and CTX assa... |