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Others 10

Others 10

Others 10 related products

Structure Cat No. Product Name CAS No. Product Description
Carboxylesterase-IN-2 V60042 Carboxylesterase-IN-2 2764748-88-9 Carboxylesterase-IN-2 (compound 4u) is a potent Carboxylesterase Notum inhibitor (antagonist) with IC50 less than or equal to 10 nM.
Cenobamate intermediate V11464 Cenobamate intermediate 1259059-71-6 Cenobamate intermediate is an intermediate used in the synthesis of cenobamate, which is medication is used to treat a certain type of seizure disorder (partial onset).
CRT-0105950 V18831 CRT-0105950 1661845-86-8 CRT0105950 is a potent LIMK inhibitor (antagonist) with IC50s of 0.3 nM and 1 nM for LIMK1 and LIMK2 inhibition, respectively.
CYM-50769 V12460 CYM-50769 1421365-63-0 CYM 50769 is a non-peptide selective antagonist of neuropeptide B/W receptor 1 (NPBWR1).
EN106 V11837 EN106 757192-67-9 EN106 is a potent FEMIB inhibitor.
Follicle-stimulating hormone V60005 Follicle-stimulating hormone 146479-72-3 Follicle-stimulating hormone (FSH) is a heterodimeric glycoprotein expressed by gonadotrophs in the anterior pituitary.
GSK484 free base V36344 GSK484 free base 1652629-23-6 GSK484 is a novel, potent, selective and reversible peptidylarginine deiminase 4 (PAD4) inhibitor which showes high affinity binding to PAD4 with IC50s of 50 nM in the absence of Calcium.
Hexakis(p-bromophenoxy)cyclotriphosphazene V34671 Hexakis(p-bromophenoxy)cyclotriphosphazene 4376-72-1 Hexakis(p-bromophenoxy)cyclotriphosphazene is a useful chemical compound.
HIF-2α Translation Inhibitor V60054 HIF-2α Translation Inhibitor 882268-69-1 HIF-2α-IN-4 is a potent HIF-2α translation inhibitor (antagonist) with IC50 of 5 μM.
IL-17 modulator 4 V17133 IL-17 modulator 4 2446803-65-0 IL-17 modulator 4 is a precursor to IL-17 modulator 1 .
IN04 V22210 IN04 838816-57-2 IN04, also know asMethyl 3-(2-((5-(3,5-dimethoxyphenyl)-1,3,4-oxadiazol-2-yl)thio)acetamido)benzoate, is a novel and potent inhibitor of Leucine rich repeat kinase 1 (LRRK1), suppressing osteoclasts (OC) function with no effect on OC formation.
KN 1022 V16229 KN 1022 205255-11-4 KN-1022 also known as1-Piperazinecarboxamide, 4-(6,7-dimethoxy-4-quinazolinyl)-N-(4-nitrophenyl)- is aBioactive molecules.
Lasmiditan succinate (COL144, LY573144) V17003 Lasmiditan succinate (COL144, LY573144) 439239-92-6 Lasmiditan succinate (COL-144, LY-573144) is a novel and selective 5-HT(1F) receptor agonist with Ki of 2.1 nM versus Ki of 1043 nM and 1357 nM at the 5-HT(1B) and 5-HT(1D) receptors, respectively.
Lecithins, egg V60064 Lecithins, egg 93685-90-6 Lecithins, egg is a novel and potent.
OATD-01 V24834 OATD-01 2088453-21-6 OATD-01 is a novel, selective andhighly active CHIT1 (chitinase1, hAMCase IC50=9nM, hCHIT1 IC50=26nM) inhibitor with both an excellent PK profile in multiple species and selectivity against a panel of other off-targets.
Ozagrel sodium V7876 Ozagrel sodium 130952-46-4 Ozagrel (also known as OKY-046) sodium salt is an antiplatelet agent working as a thromboxane A2 synthesis inhibitor.
TH-263 V34667 TH-263 313520-94-4 TH-263 is adiaryl sulfonamide derivativeused as anegative control for the type III allosteric LIM-kinase (LIMK) inhibitors TH-257, TH-255 and TH-251.
WAY-116749 V60041 WAY-116749 380872-69-5 WAY-116749 also name asEthyl 2-[[2-(3-oxo-2,4-dihydro-1H-quinoxalin-2-yl)acetyl]amino]-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate
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