All ProductsDisplaying Products by Catalog Number (1900 - 1999)
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| Cat. No. | Product Name / Activity |
|---|---|
| 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 | |
| 1908 | Neuromedin B (porcine) |
| Mammalian bombesin-like peptide | |
| 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 | |
| 1935 | Caffeic acid-pYEEIE |
| Phosphopeptide ligand for src SH2 domain | |
| 1941 | m-3M3FBS |
| Phospholipase C activator | |
| 1942 | o-3M3FBS |
| Inactive analog of m-3M3FBS (Cat. No. 1941) | |
| 1944 | Loratidine |
| Peripheral H1 antagonist; antiallergic agent | |
| 1950 | Gap 26 |
| Gap junction blocker; inhibits smooth muscle contraction and IP3-mediated ATP release | |
| 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 | |
| 1979 | L-803,087 trifluoroacetate |
| Potent and selective sst4 agonist | |
| 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 |