| Cat. No. |
Product Name & Pharmacological Action |
| 1101 | Cyclosporin A |
| Calcineurin inhibitor |
| 1102 | Procaterol hydrochloride |
| Potent β2 agonist |
| 1103 | Ketoconazole |
| Cytochrome P450c17 inhibitor |
| 1104 | 2-Cl-IB-MECA |
| Highly selective A3 agonist |
| 1105 | AF-DX 116 |
| Selective M2 antagonist |
| 1107 | ATPA |
| Selective, potent GluR5 agonist |
| 1109 | GR 103691 |
| Highly selective D3 antagonist |
| 1110 | Genistein |
| EGFR-kinase, topoisomerase kinase inhibitor |
| 1111 | ACPT-I |
| Group III mGlu agonist |
| 1112 | ACPT-II |
| Competitive mGlu receptor antagonist |
| 1114 | CGP 37157 |
| Antagonist of mitochondrial Na+/Ca2+ exchange |
| 1115 | AM 281 |
| Potent, selective CB1 antagonist/inverse agonist |
| 1116 | AM 404 |
| Anandamide transport inhibitor |
| 1117 | AM 251 |
| Potent, selective CB1 antagonist/inverse agonist |
| 1118 | Nocistatin (bovine) |
| Opposes action of nociceptin |
| 1119 | NocII |
| Orphan neuropeptide |
| 1120 | AM 630 |
| CB2 selective antagonist/inverse agonist |
| 1121 | (R)-(+)-Methanandamide |
| Potent and selective CB1 agonist |
| 1122 | Telenzepine dihydrochloride |
| Potent selective M1 antagonist |
| 1123 | (S)-(+)-Niguldipine hydrochloride |
| α1 antagonist, L-type Ca2+ channel blocker |
| 1124 | (R)-(-)-Niguldipine hydrochloride |
| Less active enantiomer of Cat. No. 1123 |
| 1125 | Quercetin |
| Non-selective PI 3-kinase inhibitor |
| 1126 | Dexamethasone |
| Anti-inflammatory glucocorticoid |
| 1127 | Yohimbine hydrochloride |
| α2-selective antagonist |
| 1128 | Picrotoxin |
| GABAA receptor antagonist |
| 1129 | BRL 54443 |
| Potent 5-ht1E/F agonist |
| 1130 | LY 294002 hydrochloride |
| Selective PI 3-kinase inhibitor |
| 1131 | KU14R |
| Antagonist of pancreatic imidazoline receptor |
| 1132 | Harmane |
| Putative endogenous imidazoline ligand. Also MAO inhibitor |
| 1133 | BRL 44408 maleate |
| Selective α2A antagonist |
| 1134 | CGP 12177 hydrochloride |
| β3 partial agonist. β1/β2 antagonist. |
| 1135 | Spermine NONOate |
| Slow NO releasing agent |
| 1136 | Okadaic acid |
| Protein phosphatase 1 and 2A inhibitor |
| 1137 | Resiniferatoxin |
| Ultrapotent vanilloid receptor agonist |
| 1138 | Thapsigargin |
| Potent inhibitor of SERCA ATPase |
| 1139 | L-NIL hydrochloride |
| Selective iNOS inhibitor |
| 1140 | 8-Bromo-cAMP, sodium salt |
| Cell-permeable cAMP analogue |
| 1141 | Dibutyryl-cAMP, sodium salt |
| Cell-permeable cAMP analogue |
| 1142 | Oxymetazoline hydrochloride |
| α1A agonist |
| 1143 | Corynanthine hydrochloride |
| α1 antagonist |
| 1144 | U0126 |
| Potent, selective inhibitor of MEK1 and 2 |
| 1145 | L-733,060 hydrochloride |
| Potent NK1 antagonist |
| 1147 | SKF 96365 hydrochloride |
| Receptor-operated calcium channel blocker |
| 1148 | Siguazodan |
| PDE3 inhibitor |
| 1149 | Bombesin |
| Involved in gastrointestinal tract function |
| 1150 | CCK Octapeptide, non-sulfated |
| Non-sulfated form of CCK octapeptide |
| 1151 | CRF (human, rat) |
| Stimulates ACTH release |
| 1152 | Neurokinin A (porcine) |
| Endogenous tachykinin peptide |
| 1153 | Neuropeptide Y (human, rat) |
| Influences feeding and sexual behaviour |
| 1154 | Pancreatic Polypeptide (human) |
| NPY Y4 agonist; involved in gastrointestinal tract function |
| 1155 | RR-src |
| Tyrosine kinase substrate peptide |
| 1156 | Substance P |
| Sensory neuropeptide, inflammatory mediator |
| 1157 | Somatostatin |
| Influences growth hormone release |
| 1158 | Angiotensin II |
| Potent vasoconstrictor peptide |
| 1159 | Calcitonin (salmon) |
| Affects bone formation and resorption |
| 1160 | Endothelin 1 (human, porcine) |
| Potent vasoconstrictor peptide |
| 1161 | CGRP (rat) |
| Potent vasodilator |
| 1162 | Endothelin 3 (human, rat) |
| Potent vasoconstrictor |
| 1163 | Saralasin |
| Non-selective angiotensin II antagonist |
| 1164 | Endothelin 2 (human) |
| ETA/ETB agonist |
| 1165 | Somatostatin 1-28 |
| Somatostatin receptor agonist |
| 1166 | CCK Octapeptide, sulfated |
| C-terminal octapeptide of CCK |
| 1167 | Leupeptin hemisulfate |
| Inhibits trypsin-like/cysteine proteases |
| 1168 | [Leu31,Pro34]-Neuropeptide Y (porcine) |
| Neuropeptide YY1 receptor agonist |
| 1169 | CGRP 8-37 (rat) |
| CGRP1 receptor antagonist |
| 1170 | DSLET |
| Selective δ agonist peptide |
| 1171 | DAMGO |
| Selective μ agonist |
| 1172 | [Ac-Tyr1,D-Phe2]GRF 1-29, amide (human) |
| VIP antagonist |
| 1173 | Neuropeptide Y (porcine) |
| Influences feeding and sexual behaviour |
| 1174 | Sarafotoxin S6b |
| Endothelin receptor agonist, non-selective |
| 1175 | Sarafotoxin S6c |
| Selective ETB agonist |
| 1176 | [Leu31,Pro34]-Neuropeptide Y (human, rat) |
| Neuropeptide YY1 receptor agonist |
| 1177 | Neuropeptide Y 13-36 (porcine) |
| Y2 receptor agonist |
| 1178 | [Sar9,Met(O2)11]-Substance P |
| Potent, selective NK1 agonist |
| 1179 | Galanin (1-30) (human) |
| Modulator of neurotransmission |
| 1180 | [D-Ala2]-Deltorphin II |
| Selective δ agonist peptide |
| 1181 | CGRP 8-37 (human) |
| CGRP1 receptor antagonist |
| 1182 | VIP (guinea pig) |
| Involved in neurotransmission, smooth muscle relaxation |
| 1183 | PACAP 1-27 |
| Potent stimulator of adenylyl cyclase |
| 1184 | α-helical CRF 9-41 |
| CRF receptor antagonist |
| 1185 | Thrombin Receptor Agonist Peptide |
| Causes platelet aggregation and secretion |
| 1186 | PACAP 1-38 |
| Potent stimulator of adenylyl cyclase |
| 1187 | GRF (ovine) |
| Stimulates growth hormone release |
| 1188 | BQ-123 |
| Selective ETA antagonist |
| 1189 | BQ-3020 |
| Selective ETB agonist |
| 1190 | Pepstatin A |
| Aspartic protease inhibitor |
| 1191 | Amyloid β-Peptide (1-40) (human) |
| Amyloid β-protein fragment |
| 1192 | Mastoparan |
| Activates Gi and Go |
| 1193 | Melittin |
| Inhibits Gs and stimulates Gi activity |
| 1194 | MDL 29,913 |
| Selective NK2 antagonist |
| 1195 | IRL-1038 |
| ETB antagonist |
| 1196 | IRL-1620 |
| Highly selective ETB agonist |
| 1197 | [Ala1,3,11,15]-Endothelin |
| Selective ETB agonist |
| 1198 | Nocistatin (human) |
| Human putative counterpart of nocistatin |
| 1199 | NF 279 |
| Potent selective P2X1 antagonist |
| 1200 | Nω-Propyl-L-arginine |
| Highly selective inhibitor of nNOS |
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