All ProductsDisplaying Products by Catalog Number (1900 - 1999)
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Cat. No. | 产品名称/活性 |
---|---|
1904 | PKA inhibitor fragment (6-22) amide |
Potent protein kinase A inhibitor | |
1906 | Atrial natriuretic factor (1-28) (human, porcine) |
Endogenous peptide regulating blood pressure | |
1909 | Neurotensin |
Endogenous neurotransmitter and endocrine modulator | |
1910 | Oxytocin |
Involved in uterine contraction and lactation | |
1911 | VIP (human, rat, mouse, rabbit, canine, porcine) |
Involved in neurotransmission and smooth muscle relaxation | |
1912 | Atrial natriuretic factor (1-28) (rat) |
Endogenous peptide regulating blood pressure | |
1918 | Secretin (human) |
Gastrointestinal peptide | |
1919 | Secretin (rat) |
Gastrointestinal peptide | |
1921 | N-Formyl-Met-Leu-Phe |
Endogenous FPR1 agonist | |
1922 | [D-Lys3]-GHRP-6 |
Ghrelin receptor antagonist | |
1932 | U 46619 |
Potent, stable thromboxane A2 (TP) receptor agonist | |
1933 | Exendin-4 |
Potent GLP-1 receptor agonist | |
1941 | m-3M3FBS |
Phospholipase C activator | |
1942 | o-3M3FBS |
Inactive analog of m-3M3FBS (Cat. No. 1941) | |
1955 | Ritanserin |
Potent 5-HT2 antagonist | |
1956 | Bestatin |
Aminopeptidase inhibitor | |
1960 | SB 334867 |
Selective non-peptide OX1 antagonist | |
1961 | SB 258585 hydrochloride |
Potent, selective 5-HT6 antagonist | |
1962 | SB 239063 |
Potent, selective p38 MAPK inhibitor; orally active | |
1963 | SB 408124 |
Selective non-peptide OX1 antagonist | |
1964 | Gossypol |
Proapoptotic; downregulates Bcl-2 and Bcl-XL | |
1965 | Simvastatin |
HMG-CoA reductase inhibitor | |
1968 | AS 19 |
Potent 5-HT7 agonist | |
1969 | SL 327 |
Selective inhibitor of MEK1 and MEK2; brain penetrant | |
1970 | Norketamine hydrochloride |
Potent non-competitive NMDA antagonist; antinociceptive | |
1971 | (+)-Anabasine hydrochloride |
High affinity nAChR partial agonist | |
1974 | SANT-1 |
Inhibitor of hedgehog (Hh) signaling; antagonizes smoothened activity | |
1980 | L-817,818 |
Potent and selective sst5 agonist | |
1982 | Reboxetine mesylate |
Potent and selective noradrenalin uptake inhibitor; orally active | |
1983 | 740 Y-P |
Cell-permeable PI 3-kinase activator | |
1984 | Nogo-66 (1-40) |
Competitive antagonist for Nogo-66 receptor; promotes neuron regeneration | |
1985 | PNU 142633 |
Highly selective 5-HT1D agonist | |
1989 | c-JUN peptide |
Peptide inhibitor of JNK/c-Jun interaction | |
1990 | (R,R)-THC |
Potent subtype-selective ligand; ERα agonist/ERβ antagonist | |
1991 | MPP dihydrochloride |
Highly selective ERα antagonist | |
1992 | Nomifensine |
Potent noradrenalin and dopamine uptake inhibitor. Antidepressant | |
1993 | Halofuginone hydrobromide |
High affinity competitive prolyl-tRNA synthetase inhibitor | |
1997 | Ro 15-4513 |
Benzodiazepine partial inverse agonist | |
1998 | JMV 449 |
Potent neurotensin receptor agonist | |
1999 | Linopirdine dihydrochloride |
KV7 (KCNQ) channel blocker |