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Biotin-VAD-FMK
Catalog No. A20384 caspase inhibitorBiotin-VAD-FMK is a cell permeable, irreversible biotin-labeled caspase inhibitor, used to identify active caspases in cell lysates. 了解更多 -
Z-IETD-FMK
Catalog No. A12800 -
Z-VDVAD-FMK
Catalog No. A12637 -
Z-FA-FMK
Catalog No. A14284 -
Z-DEVD-FMK
Catalog No. A13503 -
Z-VEID-FMK
Catalog No. A12611 Caspase-6 抑制剂Z-VEID-FMK是caspase-6 / Mch2的特异性识别序列。 Z-VEID-FMK是不可逆地抑制VEID依赖性胱天蛋白酶（例如caspase-6）活性的合成肽。 抑制剂被设计为甲酯，以促进细胞渗透性。 了解更多 -
Z-WEHD-FMK
Catalog No. A14916 -
Z-LEHD-FMK
Catalog No. A14358 -
6-Diazo-5-oxo-L-nor-Leucine
Catalog No. A20846 6-Diazo-5-oxo-L-norleucine 是一种从链霉菌中分离出来的抗生素，一种 glutaminase 的拮抗剂对cKGA（肾脏型谷氨酰胺酶）的IC50值约为1 mM。 了解更多 -
Adenosine deaminase
Catalog No. A19330 Adenosine deaminase is an enzyme that catalyzes the irreversible deamination of adenosine and 2'-deoxyadenosine to inosine and 2'-deoxyinosine, respectively. 了解更多 -
Hyaluronidase
Catalog No. A18232 local anesthetic additiveHyaluronidase (Hyaluronate 4-glycanohydrolase; Hyaluronoglucosaminidase) is a naturally occurring enzyme that depolymerizes hyaluronic acid by cleavage of glycosidic bonds and has been used as a local anesthetic additive. 了解更多 -
Cinnamylamine
Catalog No. A20835 Cinnamylamine can be used for the preparation of Tranylcypromine, a drug that acts as a nonselective and irreversible inhibitor of the enzyme monoamine oxidase (MAO), and is used as an antidepressant and anxiolytic agent. 了解更多 -
Mizagliflozin
Catalog No. A22056 SGLT1 inhibitorMizagliflozin (DSP-3235 free base) is a potent, orally active and selective SGLT1 inhibitor, with a Ki of 27 nM for human SGLT1. 了解更多 -
TLR4-IN-C34
Catalog No. A22057 TLR4 inhibitorTLR4-IN-C34 is an orally active TLR4 inhibitor and reduces systemic inflammation in models of endotoxemia and necrotizing enterocolitis. 了解更多 -
Neuraminidase-IN-1
Catalog No. A22065 neuraminidase inhibitorNeuraminidase-IN-1 is a neuraminidase inhibitor, with an IC50 of 0.21 μM. Neuraminidase-IN-1 has excellent activity against H1N1 influenza virus. 了解更多 -
Fluxapyroxad
Catalog No. A22073 the succinate dehydrogenase (SQR) enzyme inhibitorFluxapyroxad, a broad-spectrum fungicide, is an inhibitor of the succinate dehydrogenase (SQR) enzyme. 了解更多 -
FLTX1
Catalog No. A22120 antiestrogenic propertiesFLTX1 is a fluorescent Tamoxifen derivative that can specifically label intracellular Tamoxifen-binding sites (estrogen receptors) under permeabilized and non-permeabilized conditions. FLTX1 exhibits the potent antiestrogenic properties of Tamoxifen in breast cancer cells. FLTX1 is devoid of the estrogenic agonistic effect on the uterus. 了解更多 -
Epiblastin A
Catalog No. A22121 inhibitor of Casein Kinase 1 (CK1)Epiblastin A is an inhibitor of Casein Kinase 1 (CK1) that engages CK1 isoenzymes in cell lysate and induces efficient conversion of epiblast stem cells (EpiSCs) into embryonic stem cells (cESCs). 了解更多 -
(Z)-JIB-04
Catalog No. A22137 Jumonji histone demethylase inihibitorZ-JIB-04 (NSC 693627, JIB-04 Z-isomer) is an isomer of JIB-04. JIB-04 is a pan-selective Jumonji histone demethylase inihibitor with IC50 of 230 nM, 340 nM, 855 nM, 445 nM, 435 nM, 1100 nM and 290 nM for JARID1A, JMJD2E, JMJD3, JMJD2A, JMJD2B, JMJD2C, and JMJD2D, respectively. 了解更多 -
Remimazolam besylate
Catalog No. A22198 ultra short-acting benzodiazepineRemimazolam besylate is an ultra short-acting benzodiazepine used in the induction and maintenance of sedation during short (<30 minute) procedures. 了解更多 -
Zebularine
Catalog No. A12721 DNA methyltransferase inhibitorZebularine (NSC309132; 4-Deoxyuridine) is a DNA methyltransferase inhibitor. 了解更多 -
Motixafortide
Catalog No. A22276 CXCR4 antagonistMotixafortide (BKT140 4-fluorobenzoyl) is a novel CXCR4 antagonist with an IC50 vakue of ??1 nM. 了解更多 -
Amarogentin
Catalog No. A22286 bitter taste receptor TAS2R1 agonistAmarogentin (AG), a secoiridoid glycoside mainly extracted from Swertia and Gentiana roots, exhibits anti-oxidative, anti-tumour, and anti-diabetic activities. Amarogentin is an agonist for the bitter taste receptor TAS2R1 and inhibits in LAD-2 cells substance P-induced production of newly synthesized TNF-α. 了解更多 -
HA-100 dihydrochloride
Catalog No. A22289 PKs inhibitorHA-100 is an isoquinoline compound with an added piperazinylsulfonyl group that acts as an inhibitor of protein kinases (PKs), including PKA, PKC, and PKG (IC50s = 8, 12, and 4 ?M, respectively). 了解更多 -
Dorzagliatin
Catalog No. A22297 GK activatorDorzagliatin (HMS5552), a dual-acting glucokinase (GK) activator, improves glycaemic control and pancreatic β-cell function in type 2 diabetes. 了解更多 -
Benzamidine hydrochloride
Catalog No. A22323 trypsin-like serine proteases inhibitorBenzamidine hydrochloride is an reversible competitive inhibitor of trypsin-like serine proteases, with Kis of 97 ?M, 21 ?M, 20 ?M and 110 ?M for uPA, trypsin, tryptase and factor Xa, respectively. 了解更多 -
7-Nitroindazole
Catalog No. A22342 neuronal nitric oxide synthase inhibitor7-Nitroindazole, a heterocyclic compound, acts as a selective inhibitor for neuronal nitric oxide synthase showing a 10-fold selectivity for neuronal NOS. 了解更多 -
Dihydrocaffeic acid
Catalog No. A22344 Antioxidant agentDihydrocaffeic acid is a phenolic acid found in Gynura bicolor, reduces phosphorylation of MAPK p38 and prevent UVB-induced skin damage. Antioxidant potential and anti-inflammatory activity. 了解更多 -
3-Deazaadenosine hydrochloride
Catalog No. A22347 inhibitor of S-adenosylhomocysteine hydrolase3-Deazaadenosine (hydrochloride) is an inhibitor of S-adenosylhomocysteine hydrolase, with a Ki of 3.9 ?M; 3-Deazaadenosine has anti-inflammatory, anti-proliferative and anti-HIV activity. 了解更多 -
7,4'-Di-O-methylapigenin
Catalog No. A22349 antifungalThe compound 7,4'-Di-O-methylapigenin may be partly responsible for the reported antifungal activity of C. zeyheri, and may serve as a potential source of lead compounds that can be developed as antifungal phytomedicines. 了解更多
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