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Chemical Structure Cat. No. Product Name CAS No.
GO289 Chemical Structure
BCP44224 GO289 694522-87-7
GO289 is a potent and selective CK2 inhibitor.
ADH-503 Chemical Structure
BCP44222 ADH-503 2055362-72-4
ADH-503 is an orally active and allosteric CD11b agonist. ADH-503 leads to the repolarization of tumor-associated macrophages, reduction in the number of tumor-infiltrating immunosuppressive myeloid cells, and enhances dendritic cell responses.
Dimethyl carbate Chemical Structure
BCP44195 Dimethyl carbate 39589-98-5
Dimethyl carbate is an insect repellent.
Teclozan Chemical Structure
BCP44194 Teclozan 5560-78-1
Teclozan is an antiprotozoal agent employed typically as a therapy to treat protozoan infections.
WIN54954 Chemical Structure
BCP44193 WIN54954 107355-45-3
WIN 54954 is a potent antiviral agent with a highly significant effect on survival in CBV-induced myocarditis in the A/J mouse if treatment is started early.
Lu AF27139 Chemical Structure
BCP44190 Lu AF27139 2097117-06-9
Lu AF27139, a novel rodent-active and CNS-penetrant P2X7 receptor antagonist.
Lenrispodun Chemical Structure
BCP16186 Lenrispodun 1160521-50-5
ITI-214 is a potent, CNS-active, orally bioavailable PDE1 inhibitor (Ki of 58 pM) with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters and ion channels.
Lenrispodun phosphate Chemical Structure
BCP44187 Lenrispodun phosphate 1642303-38-5
ITI-214 is a potent, CNS-active, orally bioavailable PDE1 inhibitor (Ki of 58 pM) with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters and ion channels. ITI-214 inhibits recombinant full-length human PDE1A, PDE1B and PDE1C with Kis of 33 pM, 380 pM and 35 pM, respectively. ITI-214 shows efficacy in various animal models of motor and cognitive functions.
(S)-Butyl 2-hydroxybutanoate Chemical Structure
BCP44212 (S)-Butyl 2-hydroxybutanoate 132513-51-0
Hydroxy Brimonidine Chemical Structure
BCP44210 Hydroxy Brimonidine 1216379-05-3
Brimonidine Impurity 22 Chemical Structure
BCP44209 Brimonidine Impurity 22 134892-47-0
2-(2-Fluoropyridin-3-YL)acetic acid Chemical Structure
BCP44202 2-(2-Fluoropyridin-3-YL)acetic acid 1000524-26-4
Levalbuterol hydrochloride Chemical Structure
BCP44201 Levalbuterol hydrochloride 50293-90-8‬
Levalbuterol Hydrochloride is the hydrochloride salt form of levalbuterol, a relatively selective sympathomimetic beta-2 adrenergic receptor agonist with bronchodilator activity.
Ticagrelor Related Compound 2 Chemical Structure
BCP44200 Ticagrelor Related Compound 2 592533-90-9
Saxagliptin Impurity 34 Chemical Structure
BCP44198 Saxagliptin Impurity 34 2173146-31-9
Saxagliptin Impurity 19 Chemical Structure
BCP44197 Saxagliptin Impurity 19 681282-72-4
6-Bromo-4-hydroxy-pyrazolo[1,5-a]pyridine-3-carbonitrile Chemical Structure
BCP44196 6-Bromo-4-hydroxy-pyrazolo[1,5-a]pyridine-3-carbonitrile 2068065-16-5
Α-Amyrin Chemical Structure
BCP44192 Α-Amyrin 508-04-3
Difelikefalin HCl Chemical Structure
BCP44189 Difelikefalin HCl 2413256-25-2
Difelikefalin is a novel and potent kappa opioid receptor agonist.
CLEFMA Chemical Structure
BCP44188 CLEFMA 1246964-32-8
CLEFMA Activates the Extrinsic and Intrinsic Apoptotic Processes through JNK1/2 and p38 Pathways in Human Osteosarcoma Cells
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