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CRT0066101 free base
Catalog No. A22539 PRKDs inhibitorCRT0066101 is a PRKDs inhibitor. CRT0066101 suppressed the proliferation and migration of four bladder cancer cell lines in vitro. CRT0066101 blocked tumor growth in a mouse flank xenograft model of bladder cancer. 了解更多 -
MC-Gly-Gly-Phe
Catalog No. A22546 MC-Gly-Gly-Phe is a cleavable linker used for antibody-drug conjugates (ADC). 了解更多 -
Boc-Gly-Gly-Phe-Gly-OH
Catalog No. A22547 Boc-Gly-Gly-Phe-Gly-OH is a protease cleavable linker used for the antibody-drug conjugate (ADC). 了解更多 -
Boc-Dap-NE
Catalog No. A22548 Boc-Dap-NE is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). 了解更多 -
Navoximod free base
Catalog No. A22549 IDO1 inhibitorNavoximod, also known as IDO-IN-7 and NLG-1488, is an indoleamine 2,3-dioxygenase (IDO) inhibitor. 了解更多 -
ATPO
Catalog No. A22552 -
JNJ-10198409
Catalog No. A22554 PDGFRα/PDGFRβ inhbitorJNJ 10198409 is a potent platelet-derived growth factor receptor (PDGFR) inhibitor (IC50 values are 4.2 and 45 nM for PDGFRβ and PDGFRα, respectively). Also inhibits c-Abl, Lck, c-Src and Fyn kinases (IC50 values are 22, 100, 185 and 378 nM respectively). 了解更多 -
SEP-363856 HCl
Catalog No. A22555 SEP-363856, also known as SEP-856, is an orally active and CNS active psychotropic agent. 了解更多 -
MYF-01-37
Catalog No. A22556 -
L-Leucine-13C6
Catalog No. A22557 L-LEUCINE-13C6, also known as 13C6-D-Leucine or L-?Leucine-?1,?2,?3,?4,?5,?5'-?13C6, is a fully 13C labelled D-Leucine. 了解更多 -
Bractoppin
Catalog No. A22558 Bractoppin is a potent and selective inhibitor of phosphopeptide recognition by the BRCA1 tBRCT domain. 了解更多 -
LM11A-31 HCl
Catalog No. A22564 p75NTR ligandLM11A-31 is a small-molecule p75NTR modulator and proNGF antagonist. 了解更多 -
EMAC10101d
Catalog No. A22565 hCA II inhibitorEMAC10101d is a potent and selective inhibitor of Carbonic Anhydrase Isoform toward hCA II with an inhibitory activity in the low nanomolar range. Ki of 8.1 nM 了解更多 -
ARS-1323-Alkyne
Catalog No. A22566 S-IIP inhibitor/KRASG12C ProbeARS-1323-Alkyne is a novel KRASG12C occupancy probe. 了解更多 -
CC90001 free base
Catalog No. A22567 JNK inhibitorCC-90001 is a potent and selective JNK inhibitor. CC-90001 shows 12.9-fold selectivity for JNK1 over JNK2 in a cell-based model. CC-90001 can be used for the research of idiopathic pulmonary fibrosis 了解更多 -
Pizuglanstat
Catalog No. A22568 prostaglandin synthase inhibitorPizuglanstat is a hematopoietic prostaglandin synthase inhibitor. 了解更多 -
ZINC30303842
Catalog No. A22569 -
FB23 inhibitor
Catalog No. A22571 FB23 is a potent and selective inhibitor of N6-methyladenosine (m6A) demethylase FTO (fat mass and obesity associated protein). 了解更多 -
UNC-669
Catalog No. A22573 -
SNIPER(CRABP)-11
Catalog No. A22574 PROTAC degraderSNIPER(CRABP)-11, also known as PROTAC cIAP1 degrader-?4, is a potent protein degrader. 了解更多 -
Xanthurenic acid
Catalog No. A22575 II metabotropic glutamate receptor agonistXanthurenic acid is a putative endogenous Group II metabotropic glutamate receptor agonist, on sensory transmission in the thalamus. 了解更多 -
Propyl gallate
Catalog No. A22576 food antioxidantPropyl gallate is a common food antioxidant. Propyl gallate can inhibit the production of acrolein, glyoxal and methylglyoxal. 了解更多 -
Methyl dihydrojasmonate
Catalog No. A22577 fragrance ingredientMethyl dihydrojasmonate is a fragrance ingredient with a jasmine-like odor, used in many fragrance mixtures. 了解更多 -
Tetrahydropalmatine
Catalog No. A22578 analgesic agentTetrahydropalmatine, an active component isolated from corydalis, possesses analgesic effects. Tetrahydropalmatine acts through inhibition of amygdaloid release of dopamine to inhibit an epileptic attack in rats. 了解更多 -
Chelidonic acid
Catalog No. A22579 glutamate decarboxylase inhibitorChelidonic acid is a glutamate decarboxylase inhibitor, with a Ki of 1.2 μM. 了解更多 -
Flavokawain A
Catalog No. A22580 Anticancer agentFlavokawain A is found in Piper methysticum (kava plant). It suppresses expression of iNOS and COX-2 in macrophages, decreases expression of Ki67, XIAP and survivin in urothelial cell carcinoma cells, and inhibits degradation of NF-??B. 了解更多 -
Suberoyl bis-hydroxamic acid
Catalog No. A22581 HDAC1 and HDAC3 inhibitorSuberoyl bis-hydroxamic acid (Suberohydroxamic acid; SBHA) is a competitive and cell-permeable HDAC1 and HDAC3 inhibitor with ID50 values of 0.25 μM and 0.30 μM, respectively. 了解更多 -
Ethyl pyruvate
Catalog No. A22582 anti-inflammatory agentEthyl pyruvate is a simple derivative of the endogenous metabolite, pyruvic acid. Ethyl pyruvate is an anti-inflammatory agent. 了解更多 -
AT-007
Catalog No. A22588 CNS penetrant Aldose Reductase inhibitorAT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase inhibitor for treatment of Galactosemia with an IC50 value of 100 pM. AT-007 reduces toxic galactitol levels and prevents disease complications in GALT deficiency rats. 了解更多 -
Benzetimide hydrochloride
Catalog No. A22589 muscarinic acetylcholine receptor antagonistBenzetimide hydrochloride is a muscarinic acetylcholine receptor antagonist. 了解更多 -
SCH-23390 maleate
Catalog No. A22592 dopamine D1-like receptor antagonistSCH-23390 maleate (R-(+)-SCH-23390 maleate) is a potent and selective dopamine D1-like receptor antagonist with Kis of 0.2 nM and 0.3 nM for the D1 and D5 receptor, respectively. 了解更多 -
Lotamilast
Catalog No. A22594 PDE4 inhibitorLotamilast (RVT-501; E6005) is a selective phosphodiesterase 4 (PDE4) inhibitor with an IC50 of 2.8 nM. 了解更多 -
PF-06454589
Catalog No. A22595 -
NDI-091143
Catalog No. A22596 ACLY inhibitorNDI-091143 is a potent and high-affinity human ATP-citrate lyase (ACLY) inhibitor with an IC50 of 2.1 nM (ADP-Glo assay), a Ki of 7.0 nM and a Kd of 2.2 nM. 了解更多 -
Carbutamide
Catalog No. A22597 hypoglycemic agentCarbutamide (BZ-55) is an orally active and first-generation sulfonylurea with hypoglycemic activity. 了解更多 -
Quipazine maleate
Catalog No. A22600 5-HT receptor agonistQuipazine maleate is a selective 5-HT receptor agonist that promotes the proliferation and apoptosis of human hepatocyte strain of L-02 strain and could also exert an excitatory effect on raphe neurons via stimulation of 5-HT2A receptors. 了解更多
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