微信关注
China
Total item
Cart Subtotal
￥ 0.00 “sn 2”的搜索结果
-
LMPTP INHIBITOR 1 dihydrochloride
Catalog No. A22227 LMPTP inhibitorLMPTP INHIBITOR 1 (dihydrochloride) is a selective inhibitor of low molecular weight protein tyrosine phosphatase (LMPTP), with an IC50 of 0.8 μM LMPTP-A. 了解更多 -
KN-93 phosphate
Catalog No. A22229 membrane-permeant synthetic inhibitorKN-93 phosphate is a novel membrane-permeant synthetic inhibitor of purified neuronal CaMK-II, with Ki of 370 nM. 了解更多 -
LYN-1604 dihydrochloride
Catalog No. A22230 ULK1 activatorLYN-1604 dihydrochloride is a potent UNC-51-like kinase 1 (ULK1) activator (EC50=18.94 nM) for the research of triple negative breast cancer (TNBC). 了解更多 -
Almonertinib
Catalog No. A22232 EGFR inhibitorAlmonertinib (HS-10296) is an orally available, irreversible, third-generation EGFR tyrosine kinase inhibitor with high selectivity for EGFR-sensitizing and T790M resistance mutations. 了解更多 -
Enocitabine
Catalog No. A22234 DNA replication inhibitorEnocitabine is a nucleoside analog, and is a potent DNA replication inhibitor, and a DNA chain terminator. 了解更多 -
Cl-amidine TFA
Catalog No. A22235 peptidylarginine deminase (PAD) inhibitorCl-amidine TFA is an orally active peptidylarginine deminase (PAD) inhibitor, with IC50 values of 0.8 μM, 6.2 μM and 5.9 μM for PAD1, PAD3, and PAD4, respectively. 了解更多 -
Taletrectinib
Catalog No. A22237 ROS1/NTRK inhibitorTaletrectinib (DS-6051b) is a potent, orally active, and new-generation selective ROS1/NTRK inhibitor. 了解更多 -
LY-3475070
Catalog No. A22239 CD73 InhibitorLY-3475070 is a potent and selective CD73 Inhibitor with IC50 of 28 nM. 了解更多 -
Mobocertinib succinate
Catalog No. A22240 EGFR/HER2 oncogenic mutants inhibitorMobocertinib succinate (TAK-788 succinate) is a potent and orally active inhibitor of EGFR and HER2 oncogenic mutants, including exon 20 insertions, with selectivity over WT EGFR. Antitumor activity. 了解更多 -
ML-335
Catalog No. A22244 OPRM1(μ-opioid receptor)-OPRD1(δ-opioid receptor) heterodimerization agonistML335 (CYM 51010, CID-23723457) is an agonist for OPRM1(μ-opioid receptor)-OPRD1(δ-opioid receptor) heterodimerization with EC50 of 403 nM demonstrating selectivity over the individual OPRM1 and OPRD1 receptors and the serotonin HT5A receptor with EC50 of 14.9 μM, 1.1 μM, and >40 μM, respectively. 了解更多 -
Imidazenil
Catalog No. A22247 GABA-A modulatorImidazenil is a GABA-A modulator that blocks the sedative effects without lowering the convulsion threshold. 了解更多 -
TSPC (HUN86320)
Catalog No. A22250 inhibitor for GA perceptionTSPC is an inhibitor for GA perception by in vitro and in planta evaluations. 了解更多 -
Imidacloprid-urea
Catalog No. A22253 marine xenobiotic metaboliteImidacloprid-urea with a role as a marine xenobiotic metabolite, is the primary imidacloprid soil metabolite, whereas imidacloprid-olefin is the main plant-relevant metabolite and is more toxic to insects than imidacloprid. 了解更多 -
Finasteride Carboxaldehyde
Catalog No. A22255 used for proteomics researchFinasteride Carboxaldehyde is a metabolite of Finasteride in human bile (M2 metabolite) that can be used for proteomics research. 了解更多 -
CFI-400945
Catalog No. A22256 PLK4 inhibitorCFI-400945 is an orally active, potent and selective polo-like kinase 4(PLK4) inhibitor with Ki value of 0.26 nM. 了解更多 -
Salvinorin B
Catalog No. A22257 analytical reference material categorizedSalvinorin B (Item No. 11488) is an analytical reference material categorized as a diterpene. 了解更多 -
(R)-Propranolol hydrochloride
Catalog No. A22258 β-adrenergic receptor (βAR) antagonist(R)-Propranolol hydrochloride is a less active enantiomer of the β-adrenoceptor antagonist propranolol (HY-B0573). Propranolol is a nonselective β-adrenergic receptor (βAR) antagonist, has high affinity for the β1AR and β2AR with Ki values of 1.8 nM and 0.8 nM, respectively. 了解更多 -
Clenproperol
Catalog No. A22259 -
Propachlor
Catalog No. A22260 LDH1A1 inhibitorPropachlor is a specific ALDH1A1 inhibitor. It is sometimes used as an herbicide. 了解更多 -
N-(beta-Ketocaproyl)-L-hoMoserine lactone
Catalog No. A22261 autoinducer of P. fischeri luciferaseN-(beta-ketocaproyl)-L-Homoserine lactone (N-(Ketocaproyl)-L-homoserine lactone, N-(β-Ketocaproyl)-L-hoMoserine lactone) is an autoinducer of P. fischeri luciferase and a component of quorum regulatory sensing. 了解更多 -
AG-1478 hydrochloride
Catalog No. A22262 EGFR tyrosine kinase inhibitorAG-1478 hydrochloride (Tyrphostin AG-1478 hydrochloride) is a selective EGFR tyrosine kinase inhibitor with IC50 of 3 nM. 了解更多 -
Ferulic acid methyl ester
Catalog No. A22364 antioxidant agentFerulic acid methyl ester (Methyl Ferulate, Methyl 4'-hydroxy-3'-methoxycinnamate) is a lipophilic derivative of ferulic acid, which is a hydroxycinnamic acid that is abundant in plants. It shows the strongest antioxidant activity and can protect against inflammation and cancer. 了解更多 -
7-Hydroxy-4H-chromen-4-one
Catalog No. A22365 Src kinase inhibitor7-Hydroxychromone is a Src kinase inhibitor with an IC50 of <300 μM. 了解更多 -
6-(Dimethylamino)purine
Catalog No. A22366 dual inhibitor of protein kinase and CDK6-(Dimethylamino)purine is a dual inhibitor of protein kinase and CDK. 了解更多 -
Mitapivat
Catalog No. A22367 -
Iso-H7 dihydrochloride
Catalog No. A22368 inhibitor of phosphokinase CIso-H7 dihydrochloride is an inhibitor of phosphokinase C. 了解更多 -
PF-562271 hydrochloride
Catalog No. A22370 FAK and Pyk2 kinase inhibitorPF-562271 hydrochloride is a potent, ATP-competitive and reversible FAK and Pyk2 kinase inhibitor with IC50s of 1.5 nM and 13 nM, respectively. 了解更多 -
SAR-020106
Catalog No. A22371 CHK1 inhibitorSAR-020106 is an ATP-competitive, potent, and selective CHK1 inhibitor with an IC50 of 13.3 nM for human CHK1. 了解更多 -
Nemiralisib
Catalog No. A22373 PI3Kδ inhibitorNemiralisib (GSK2269557 free base) is a potent and highly selective PI3Kδ inhibitor with a pKi of 9.9. 了解更多 -
Tirabrutinib hydrochloride
Catalog No. A22375 BTK inhibitorTirabrutinib (ONO-4059) hydrochloride is a selective and novel inhibitor of BTK with IC50 2.2 nm, Tirabrutinib binds to BTK within B cells, thereby preventing B-cell receptor signaling and impeding B-cell development. 了解更多 -
Miransertib hydrochloride
Catalog No. A22376 Akt inhibitorMiransertib hydrochloride (ARQ-092 hydrochloride) is a potent, orally active, selective and allosteric Akt inhibitor with IC50s of 2.7 nM, 14 nM and 8.1 nM for Akt1, Akt2, Akt3, respectively. 了解更多 -
PF-06273340
Catalog No. A22377 pan-Trk inhibitorPF-06273340 is a highly potent, kinases elective, well-tolerated pan-Trk inhibitor with IC50 values of 6, 4, 3 nM for TrkA, TrkB, Trk C, respectively. 了解更多 -
VPS34 inhibitor 1 (Compound 19)
Catalog No. A22378 VPS34 inhibitorVPS34 inhibitor 1 (Compound 19, PIK-III analogue) is a potent and selective inhibitor of VPS34 with an IC50 of 15 nM. 了解更多
联系我们
United StatesAdooq Bioscience
Toll Free: (866) 930-6790
Fax: +1-323-606-8156
Email: sales@adooq.com
Not your Region? View all Distributors
ADOOQ 产品质量保证
We promise all products to perform as described.