Name | Description | Size | Catalog # | Supplier | |
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A1120 | n/a | n/a | A3111 |
MILLIPORE-SIGMA |
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A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 10 mg | A-345 |
ALOMONE LABS |
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A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 25 mg | A-345 |
ALOMONE LABS |
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A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 5 mg | A-345 |
ALOMONE LABS |
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A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 50 mg | A-345 |
ALOMONE LABS |
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A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 10 mg | A-225 |
ALOMONE LABS |
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A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 100 mg | A-225 |
ALOMONE LABS |
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A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 25 mg | A-225 |
ALOMONE LABS |
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A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 250 mg | A-225 |
ALOMONE LABS |
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A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 5 mg | A-225 |
ALOMONE LABS |
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A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 50 mg | A-225 |
ALOMONE LABS |
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A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 1 mg | A-360 |
ALOMONE LABS |
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A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 10 mg | A-360 |
ALOMONE LABS |
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A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 25 mg | A-360 |
ALOMONE LABS |
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A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 5 mg | A-360 |
ALOMONE LABS |
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A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 1 mg | A-600 |
ALOMONE LABS |
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A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 10 mg | A-600 |
ALOMONE LABS |
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A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 10 x 1 mg | A-600 |
ALOMONE LABS |
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A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 5 mg | A-600 |
ALOMONE LABS |
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A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 5 x 5 mg | A-600 |
ALOMONE LABS |
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A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 10 mg | A-420 |
ALOMONE LABS |
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A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 100 mg | A-420 |
ALOMONE LABS |
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A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 25 mg | A-420 |
ALOMONE LABS |
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A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 50 mg | A-420 |
ALOMONE LABS |
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A-794278 | A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 10 mg | A-435 |
ALOMONE LABS |
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