Tel: | +86-21-31433387 |
+86-15618786686 | |
Email: | sales@rechemscience.com |
info@rechemscience.com | |
QQ: | 1369748377 |
Skype: | sales@rechemscience.com |
Cat.No. | Product name | Product Description |
R10793 | (-)-JQ1 | The bromodomain and extra terminal domain (BET) family of proteins, including BR |
R10794 | Capadenoson; BAY 68-4986 | Capadenoson (BAY 68-4986) is a new adenosine A1 receptor agonist. |
R10797 | CWHM-12 | CWHM-12 a novel small molecule inhibitor of αV integrins with IC50s of 1.8/0.8/1 |
R10799 | LCL161 Enantiomer | LCL161 is an orally bioavailable second mitochondrial-derived activator of caspa |
R10801 | Deltarasin | Deltarasin is a small molecular inhibitor of KRAS-PDEδ interaction with Kd of 38 |
R10802 | Nutlin-3 | MDM2 antagonist nutlin-3 is a potent inducer of apoptosis. |
R10803 | PX478 dihydrochloride | PX-478 2HCl is an orally active, and selective hypoxia-inducible factor-1α (HIF- |
R10804 | INNO-206; Aldoxorubicin HCl | |
R10805 | Elacridar HCl | Elacridar hydrochloride is a P-glycoprotein inhibitor, and has been used both in |
R10808 | PTZ-343; phenothiazine sodium salt | PTZ-343 is a phenothiazine derivative with chemical name: sodium 3-(10H-phenothi |
R10809 | Golotimod; SCV 07 | Golotimod is an orally bioavailable synthetic peptide containing the amino acids |
R10810 | Uramustine | Uramustine is a chemotherapy drug which belongs to the class of alkylating agent |
R10813 | ARRY-520 | KSP inhibitor ARRY-520 specifically inhibits KSP (kinesin-5 or Eg5) with potenti |
R10814 | Muscimol HBr | Muscimol hydrobromide is a potent but toxic structural analog of g-aminobutyric |
R10815 | Oprozomib (ONX 0912; PR047) | Oprozomib (ONX 0912) is an orally bioavailable inhibitor for CT-L activity of 20 |
R10816 | Tretazicar (CB 1954) | Tretazicar (CB 1954), an antitumor prodrug, is highly selective against the Walk |
R10817 | Pelitrexol | Pelitrexol (AG 2037) is an inhibitor of glycinamide ribonucleotide formyltransfe |
R10818 | Varlitinib; ARRY 543 | Varlitinib is a selective and potent ErbB1(EGFR) and ErbB2(HER2) inhibitor with |
R10820 | RO08-2750 | Ro 08-2750 is a non-peptide and reversible nerve growth factor (NGF) i |
R10821 | (1R,2R)-2-fluorocyclopropanecarboxylic acid | |
R10822 | PTZ-343 | PTZ-343 is a phenothiazine derivative with chemical name: sodium 3-(10H-phenothi |
R10823 | BOC-4-HYDROXY-L-PYRROLIDINE LACTONE | |
R10825 | Gemcitabine elaidate(CP-4126; CO-101) | Gemcitabine elaidate(CP-4126; CO-101) is a lipophilic, unsaturated fatty acid es |
R10827 | RG7112 (Synonyms: RO5045337) | RG7112 is the first clinical small-molecule MDM2 inhibitor designed to occupy th |
R10828 | HO-3867 | HO-3867, an analog of curcumin, is a selective STAT3 inhibitor. |