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Ca2+ ChannelÀ» blocking ½ÃŰ´Â compound¸¦ ¼Ò·® ¸ð¾Æ °æÁ¦ÀûÀÎ kit·Î °ø±ÞÇÕ´Ï´Ù. |
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| Alomone labs | |||
| Compound | Properties | Cat No. | M.W. | Solubility | Specific Ca 2+ Channel Blockage Activity and Recommended Effective Concentrations |
Recommended References |
|---|---|---|---|---|---|---|
| ¥ø-Agatoxin IVA | Agelenopsis aperta 5 ¥ìg (>99%) | A-500 | 5202 | Water | P-/Q-types; 20 nM-1 ¥ìM | Mintz.I.M. et al. (1992) Nature 355, 827. |
| ¥ø-Agatoxin TK | Agelenopsis aperta 5 ¥ìg (>99%) | A-530 | 5273 | Water | P-/Q-types; 20 nM-1 ¥ìM | Teramoto, T. et al. (1995) Neuroreport 6, 1684. |
| (¡¾)-Bay K 8644 | 1 mg (>99%) | B-350 | 356.3 | DMSO | Active L-type, voltage-gated Ca2+ channel agonist; 1 ¥ìM. | Hes, P. et al. (1984) Nature 311, 538. Nowycky, M.C. et al. (1985) PNAS USA 82, 2178. |
| Calcicludine | Dendroaspis angusticeps 70 ¥ìg (>98%) | C-650 | 6979 | Water | Neuronal L-type; 1-10nM | Schweitz, H. et al. (1994) P.N.A.S. USA 91, 878. |
| Calciseptine | Dendroaspis p. polylepis 70 ¥ìg (>98% | C-500 | 7036 | Water | L-type; 100nM-2¥ìM | De Weille, J.R. et al. (1991) P.N.A.S. USA 88, 2437. |
| ¥ø-Conotoxin GVIA | Conus geographus 0.1 mg (>99%) | C-300 | 3037 | Water | N-type; 100nM-1¥ìM | Olivera, B.M. et al. (1985) Science 230, 1338. |
| ¥ø-Conotoxin MVIIA | Conus magus 50 ¥ìg (>99%) | C-670 | 2639 | Water | N-type (reversible); 100nM-2¥ìM | Olivera, B.M. et al. (1987) Biochemistry 26, 2086. |
| ¥ø-Conotoxin MVIIC | Conus magus 30 ¥ìg (>99%) | C-150 | 2756 | Water | Q-type, 50nM-1¥ìM | Hillyard, D.R. et al. (1992) Neuron 9, 69. |
| FS-2 | Dendroaspis p. polylepis 70 ¥ìg (>98%) | F-700 | 7004 | Water | L-type; 100nM-2¥ìM. | Jean-Pierre, A. et al. (1995) Biochemistry 34, 5923. Wanatabe, T.X. et al. (1995) Jpn. J. Pharmacol. 68, 305. |
| ¥ø-Grammotoxin SIA | Grammostola spatulata 5 ¥ìg (>98%) | G-450 | 4113 | Water | N-type, P-type; ¥ø-Grammotoxin SIA potently inhibits both CaV2.1 (P-type) and CaV2.2 (N-type) channels by altering the voltage-dependence of channel gating. |
Lampe R. A., et al.,(1993) Mol. Pharmacol. 44, 451. Piser T. M., et al.,(1995) Mol. Pharmacol. 48, 131. McDonough S. I., et al.,(1997) Mol. Pharmacol. 52, 1095. |
| Nifedipine | 100 mg (>98%) | 346.34 | DMSO | L-type; 1-10 ¥ìM |
Triggle, D.J. & Janis, R.A. (1987) Annu. Rev. Pharmacol. Toxicol. 27, 34. |
|
| Nimodipine | 5 mg (>99%) | 418.5 | Methanol | L-type; 1-2 ¥ìM |
Triggle, D.J. & Janis, R.A. (1987) Annu. Rev. Pharmacol. Toxicol. 27, 34 |
|
| Pimozide | 5 mg (>98%) | 461.6 | DMSO | T-type channel blocker, IC50=40 nM for CaV3.1-3 expressed in HEK cells. In Xenopus oocytes IC50=3 ¥ìM for CaV3.1. | Santi, C.M. et al. (2002) J. Neurosci. 22, 396. | |
| PLTX-II | Plectreurys tristes 5 ¥ìg (>99%) | P-510 | 5109 | Water | Insect neuronal types, 10-50 nM | Leung, H.-T. et al. (1989) Neuron 3, 767. |
| SNX-482 | Hysterocrates gigas 5 ¥ìg (>98%) | S-500 | 4495 | Water | R-type channel blocker: IC50=15-30 nM. |
Newcomb, R. et al. (1998) Biochemistry 37,15353. Bourniet, E. et al. (2001) Biophys. J. 81, 79. Wang, G. et al. (1999) J. Neurosci. 19, 9235. |
| TaiCatoxin | Oxyuranus s. scutellatus 0.1 mg (>97%) | T-800 | 52,000 | Water | L-type; 50-500nM | Possani, L.D. et al. (1992) Toxicon 30, 1343. |
| Compound | Properties | Cat No. | M.W. | Solubility | Specific Ca 2+ Channel Blockage Activity and Recommended Effective Concentrations |
Recommended References |
|---|---|---|---|---|---|---|
| Amlodipine besylate | 10 mg > 99% | A-120 | 567.1 | DMSO |
1 - 100 ¥ìM L-type and T-type Ca2+channels |
Burges, R. A. et al. (1987) J. Cardiovasc. Pharmacol. 9,110. Julius, S. et al. (2004) The Lancet 363, 2022. Furukawa, T. et al. (2005) J. Cardiovasc. Pharmacol. 45, 241. |
| Felodipine | 5 mg > 99% | F-105 | 384.25 | DMSO |
1-10 ¥ìm L-type Ca2+ channels |
Furukawa, T. et al. (1999) J.P.E.T. 291,464. Furukawa, T. et al. (2005) J. Cardiovasc. Pharmacol. 45, 241. |
| Flunarizine dihydrochloride | 1 g > 99% | F-110 | 477.4 | DMSO |
1 - 200 ¥ìM L-type Channels |
Todd, P.A. and Benfield, P. (1989) Drugs. 38, 481. Tytgat, J. et al. (1988) Naunyn-Schmiedeberg's Arch.Pharmacol. 337, 690. |
| Isradipine | 5 mg > 99% | I-100 | 371.4 | DMSO |
50 nM - 5 ¥ìM L-type Channels |
Ganz, M. et al. (2005) J. Clin. Hypertens. 7, 27. Berjukow, S. et al. (2007) J. Biol. Chem. 275, 22114. Chan, C.S. et al. (2007) Nature 447, 1081. |
| L-651,582 | 5 mg > 99%. | L-110 | 424.7 | DMSO | 0.5 - 200 ¥ìM L-type Channels |
1. Hupe, D.J. et al. (1991) J. Biol. Chem. 266, 10136. 2. Guo, L. et al. (1991) Eur. J. Pharmacol. 538, 15. |
| Nicardipine HCl | 1 g > 99% | N-125 | 567.1 | DMSO |
1 - 100 ¥ìM L-type and T-type Ca2+ channels |
Ishikawa, T. et al. (1993) Circ. Res. 73, 1128. Sorkin, E.M. and Clissold, S. P. (1987) Drugs 33, 296. Furukawa, T. et al. (2005) J. Cardiovasc. Pharmacol. 45, 241 |
| Nifedipine | 1 g > 99.8%. | N-120 | 346.3 | DMSO | 0.1 - 10 ¥ìM L-type Cav channels |
Furukawa, T. et al. (1999) J. Pharmacol. Exp.Ther. 291, 464. Sorkin, E.M. et al. (1985) Drugs 30, 182. Lundy, A. et al. (2009) Vasc. Health Risk Mang. 5, 429. |
| Nimodipine | 50 mg > 99% | N-150 | 418.4 | DMSO |
0.1 - 100 ¥ìM L-type Cav channels |
Cohen, C.J. and McCarthy, R.T. (1987) J. Physiol. 387, 195. McCarthy, R.T. and Cohen, C.J. (1989) J. Gen. Physiol. 94, 669. Furukawa, T. et al. (1999) J.Pharmacol. Exp.Ther. 291, 464. Furukawa, T. et al. (2005) J. Cardiovasc. Pharmacol. 45, 241. |
| PD 173212 | 5 mg > 99% | P-105 | 599.9 | DMSO |
10 nM - 10 ¥ìM N-type Cav channels |
Hu, L.Y. et al. (1999) Bioorg. Med. Chem. Lett. 9, 2151 |
| Verapamil HCl | 1 g > 99% | V-100 | 491.1 | DMSO | 1 ¥ìM - 250 ¥Ìm |
Zanchetti, A. et al. (1998) J. Hypertension 16, 1667. Hockerman, G. H. et al. (1997) Annu. Rev. Pharmacol. Toxicol. 37, 361. Lacinova, L. et al. (1995) J. Pharmacol. Exp. Ther. 274, 54. Huber, I.G. et al. (2004) J. Biol. Chem. 279, 55211. |