Prulifloxacin |
A prodrug from of ulifloxacin; increases survival in various mouse models… |
250 mg |
31624-250 |
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Prulifloxacin |
A prodrug from of ulifloxacin; increases survival in various mouse models… |
5 g |
31624-5 |
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Prulifloxacin |
A prodrug from of ulifloxacin; increases survival in various mouse models… |
500 mg |
31624-500 |
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Prunetin |
An isoflavone with diverse biological activities; an allosteric inhibitor… |
10 mg |
29432-10 |
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Prunetin |
An isoflavone with diverse biological activities; an allosteric inhibitor… |
25 mg |
29432-25 |
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Prunetin |
An isoflavone with diverse biological activities; an allosteric inhibitor… |
5 mg |
29432-5 |
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Prunin |
A flavonoid glycoside with diverse biological activities; inhibits NA acti… |
1 mg |
34034-1 |
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Prunin |
A flavonoid glycoside with diverse biological activities; inhibits NA acti… |
10 mg |
34034-10 |
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Prunin |
A flavonoid glycoside with diverse biological activities; inhibits NA acti… |
5 mg |
34034-5 |
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PRX-08066 |
A 5-HT2B receptor antagonist; binds to 5-HT2B receptors (Ki = 3.4 nM); inh… |
1 mg |
31477-1 |
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PRX-08066 |
A 5-HT2B receptor antagonist; binds to 5-HT2B receptors (Ki = 3.4 nM); inh… |
10 mg |
31477-10 |
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PRX-08066 |
A 5-HT2B receptor antagonist; binds to 5-HT2B receptors (Ki = 3.4 nM); inh… |
5 mg |
31477-5 |
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PS-1145 |
An IKKβ inhibitor (IC50 = 88 nM); selectively inhibits IKKβ over… |
1 mg |
14862-1 |
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PS-1145 |
An IKKβ inhibitor (IC50 = 88 nM); selectively inhibits IKKβ over… |
5 mg |
14862-5 |
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PS-1145 |
An IKKβ inhibitor (IC50 = 88 nM); selectively inhibits IKKβ over… |
500 µg |
14862-500 |
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PS-210 |
An activator of PDK1; selective for PDK-1 over a panel of 120 kinases at 1… |
1 mg |
30923-1 |
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PS-210 |
An activator of PDK1; selective for PDK-1 over a panel of 120 kinases at 1… |
10 mg |
30923-10 |
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PS-210 |
An activator of PDK1; selective for PDK-1 over a panel of 120 kinases at 1… |
5 mg |
30923-5 |
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PSB-12379 |
An inhibitor of CD73 (Kis = 2.21 and 9.03 nM for the recombinant human and… |
1 mg |
28446-1 |
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PSB-12379 |
An inhibitor of CD73 (Kis = 2.21 and 9.03 nM for the recombinant human and… |
10 mg |
28446-10 |
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PSB-12379 |
An inhibitor of CD73 (Kis = 2.21 and 9.03 nM for the recombinant human and… |
5 mg |
28446-5 |
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PSB-603 |
An adenosine A2B receptor antagonist (Ki = 0.553 nM); selective for adenos… |
1 mg |
25637-1 |
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PSB-603 |
An adenosine A2B receptor antagonist (Ki = 0.553 nM); selective for adenos… |
10 mg |
25637-10 |
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PSB-603 |
An adenosine A2B receptor antagonist (Ki = 0.553 nM); selective for adenos… |
25 mg |
25637-25 |
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PSB-603 |
An adenosine A2B receptor antagonist (Ki = 0.553 nM); selective for adenos… |
5 mg |
25637-5 |
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PSB-CB5 |
A GPR18 antagonist; 36-, 36-, and 14-fold selective for GPR18 over GPR55,… |
10 mg |
35279-10 |
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PSB-CB5 |
A GPR18 antagonist; 36-, 36-, and 14-fold selective for GPR18 over GPR55,… |
25 mg |
35279-25 |
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PSB-CB5 |
A GPR18 antagonist; 36-, 36-, and 14-fold selective for GPR18 over GPR55,… |
5 mg |
35279-5 |
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PSB-KD107 |
A GPR18 agonist (EC50 = 0.56 µM in a β-arrestin recruitment ass… |
1 mg |
31393-1 |
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PSB-KD107 |
A GPR18 agonist (EC50 = 0.56 µM in a β-arrestin recruitment ass… |
10 mg |
31393-10 |
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PSB-KD107 |
A GPR18 agonist (EC50 = 0.56 µM in a β-arrestin recruitment ass… |
5 mg |
31393-5 |
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PSB-1115 (potassium salt) |
An adenosine A2B receptor antagonist (Ki = 53.4 nM); selective for A2B ove… |
10 mg |
23929-10 |
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PSB-1115 (potassium salt) |
An adenosine A2B receptor antagonist (Ki = 53.4 nM); selective for A2B ove… |
25 mg |
23929-25 |
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PSB-1115 (potassium salt) |
An adenosine A2B receptor antagonist (Ki = 53.4 nM); selective for A2B ove… |
5 mg |
23929-5 |
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PSB-SB1202 |
A CB1 and CB2 agonist with EC50 values of 56 and 14 nM, respectively; sele… |
1 mg |
15621-1 |
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PSB-SB1202 |
A CB1 and CB2 agonist with EC50 values of 56 and 14 nM, respectively; sele… |
10 mg |
15621-10 |
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PSB-SB1202 |
A CB1 and CB2 agonist with EC50 values of 56 and 14 nM, respectively; sele… |
5 mg |
15621-5 |
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PSC 833 |
A multidrug-resistance modulator; restores sensitivity of MDR-P388 murine… |
1 mg |
20391-1 |
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PSC 833 |
A multidrug-resistance modulator; restores sensitivity of MDR-P388 murine… |
10 mg |
20391-10 |
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PSC 833 |
A multidrug-resistance modulator; restores sensitivity of MDR-P388 murine… |
5 mg |
20391-5 |
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PSC 833 |
A multidrug-resistance modulator; restores sensitivity of MDR-P388 murine… |
500 µg |
20391-500 |
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P-Selectin/CD62P (human, recombinant) |
Source: Active recombinant C-terminal human IgG1 Fc-tagged P-selectin expr… |
1 mg |
35508-1 |
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P-Selectin/CD62P (human, recombinant) |
Source: Active recombinant C-terminal human IgG1 Fc-tagged P-selectin expr… |
100 µg |
35508-100 |
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P-Selectin/CD62P (mouse, recombinant) |
Source: Active recombinant C-terminal His-tagged P-selectin expressed in H… |
1 mg |
35728-1 |
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P-Selectin/CD62P (mouse, recombinant) |
Source: Active recombinant C-terminal His-tagged P-selectin expressed in H… |
100 µg |
35728-100 |
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P-Selectin Glycoprotein Ligand-1/CD162 Extracellular Domain (human, recombinant; His- and Fc-tagged) |
Source: Recombinant C-terminal human IgG1 Fc-His-tagged PSGL-1 extracellul… |
100 µg |
38062-100 |
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P-Selectin Glycoprotein Ligand-1/CD162 Extracellular Domain (human, recombinant; His-tagged) |
Source: Recombinant human C-terminal His-tagged PSGL-1 expressed in HEK293… |
1 mg |
38072-1 |
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P-Selectin Glycoprotein Ligand-1/CD162 Extracellular Domain (human, recombinant; His-tagged) |
Source: Recombinant human C-terminal His-tagged PSGL-1 expressed in HEK293… |
100 µg |
38072-100 |
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Pseudoephedrine-d3 (hydrochloride) |
An internal standard for the quantification of pseudoephedrine by GC- or L… |
100 µg |
22494-100 |
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Pseudoephedrine tert-butyl Carbamate |
An analytical reference standard categorized as an amphetamine; a precurso… |
1 mg |
22741-1 |
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