Cat. No. | Product name | CAS No. |
DC10260 |
Prochlorperazine
Prochlorperazine is a dopamine (D2) receptor antagonist that belongs to the phenothiazine class of antipsychotic agents. It is also a highly potent typical antipsychotic. |
58-38-8 |
DC25055 |
Prodigiosin
Featured
Prodigiosin is a natural red pigment produced by numerous bacterial species, has exhibited promising anticancer activity. |
82-89-3 |
DC20192 |
Proflavine;3,6-Diaminoacridine
Proflavine is a disinfectant bacteriostatic against many gram-positive bacteria. It is a topical antiseptic used mainly in wound dressings. |
92-62-6 |
DC20511 |
proMMP9-IN-3c
proMMP9-IN-3c is a potent and specific inhibitor of the hemopexin-like domain of MMP-9 (proMMP-9) with Kd of 320 nM. |
2138321-18-1 |
DC8670 |
Propanil
Propanil is a widely used contact herbicide, mainly use in rice production. |
709-98-8 |
DC12210 |
Propionylcarnitine
Propionylcarnitine is a propionyl ester of L-carnitine. |
17298-37-2 |
DCAPI1163 |
Prostaglandin E2 (Cervidil)
Featured
Prostaglandin E2 is a hormone-like substance that participate in a wide range of body functions such as the contraction and relaxation of smooth muscle, the dilation and constriction of blood vessels, control of blood pressure, and modulation of inflammation. |
363-24-6 |
DC12248 |
PROTAC BET degrader-2
PROTAC BET degrader-2 is a highly potent degrader of Bromodomain and Extra-Terminal (BET) proteins with an IC50 value of 9.6 nM in cell growth inhibition in the RS4;11 cells and capable of achieving tumor regression. |
2093388-33-9 |
DC12171 |
PROTAC Linker 2
PROTAC Linker 2 is a PROTAC linker utilized to connect the respective tyrosine kinase inhibitor (TKI) to the E3 recruiting ligand. |
1835705-52-6 |
DC12264 |
Protac linker 5
Protac Linker 5 is a PROTAC linker utilized to connect the respective tyrosine kinase inhibitor (TKI) to the E3 recruiting ligand. |
2245697-83-8 |
DC21535 |
proTAME
proTAME is a cell permeable prodrug of TAME, which is an anaphase-promoting complex/cyclosome (APC/C) inhibitor that binds to the APC preferentially suppresses APC/C(Cdc20). |
1362911-19-0 |
DC6903 |
Lapaquistat Acetate (TAK-475)
Protective effects of a squalene synthase inhibitor, lapaquistat acetate (TAK-475), on statin-induced myotoxicity in guinea pigs. |
189060-13-7 |
DC10241 |
Protirelin
Featured
Protirelin is a tripeptide that stimulates the release of thyrotropin and prolactin. |
24305-27-9 |
DC20172 |
Proxyphylline; Monophylline, Spasmolysin
Proxyphylline is a derivative of theophylline which is used as a bronchodilator and for its cardiovascular properties. It selectively antagonizes A1 adenosine receptors (Ki = 82 nM for bovine brain) versus A2 adenosine receptors (Ki = 850 µM for platelets |
603-00-9 |
DC7254 |
PRT062607
PRT062607(P505-15) anti-SYK activity is at least 80-fold greater than its affinity For other kinases. at least 80-fold greater than its affinity For other kinases. PRT062607 potently inhibits B cell antigen receptor-mediated B cell signaling and activation (IC50 0.27 and 0.28 μM, respectively) and Fcε receptor 1-mediated basophil degranulation (IC50 0.15 μM). PRT062607 inhibits BCR-dependent secretion of the chemokines CCL3 and CCL4 by CLL cells, and leukemia cell migration toward the tissue homing chemokines CXCL12, CXCL13, and beneath stromal cells. PRT062607 furthermore inhibits Syk and extracellular signal-regulated kinase phosphorylation after BCR triggering. For the detailed information of PRT062607, the solubility of PRT062607 in water, the solubility of PRT062607 in DMSO, the solubility of PRT062607 in PBS buffer, the animal experiment (test) of PRT062607, the cell expriment (test) of PRT062607, the in vivo, in vitro and clinical trial test of PRT062607, the EC50, IC50,and Affinity of PRT062607, Please contact DC Chemicals.. |
1370261-97-4 |
DC4147 |
Prucalopride
Featured
Prucalopride is a selective, high affinity 5-HT receptor agonistfor 5-HT4a and 5-HT4b with Ki of 2.5 nM and 8 nM, respectively. |
179474-81-8 |
DC8289 |
Prucalopride succinate
Prucalopride succinate is a selective, high affinity 5-HT4 receptor agonist with pKi of 8.6/8.1 for 5-HT4a/4b. |
179474-85-2 |
DC9979 |
PRX-08066
Featured
PRX-08066 is a selective 5-hydroxytryptamine receptor 2B (5-HT2BR, IC50= 3.4 nM) antagonist that causes selective vasodilation of pulmonary arteries. |
866206-54-4 |
DC21536 |
PS210
Featured
PS 210 is a potent, specific activator of PDK1 that target the PIF-binding pocket of PDK1, does not alter the activity of any of the 121 kinases (S6K, PKB/Akt or GSK3).. |
1221962-86-2 |
DC21537 |
PS 423
PS 423 is a substrate-selective inhibitor of PDK1, inhibits the phosphorylation and activation of S6K without affecting the PKB/Akt signaling pathway in HEK293 cells, the prodrug of PS210. |
1221964-37-9 |
DC23286 |
PS1
PS1 is a potent inhibitor of IAP family with IC50 of 36/96/33 nM for c-IAP1/c-IAP2/XIAP respectively.. |
1207994-72-6 |
DC21468 |
PS10
PS10 (PDK inhibitor PS10) is a novel potent and highly selective pyruvate dehydrogenase kinase (PDK) inhibitor. |
1564265-82-2 |