| A-966492 |
A-966492 is a highly potent and efficacious poly(ADP-ribose) polymerase (PARP) inhibitor with a Ki and EC50 of 1 nM. Purity is greater than 99%. |
10 mg |
orb60826 |
 BIORBYT LTD. |
More Info
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| A23187 |
A calcium ionophore. Causes rapid influx of calcium in various cells. |
10 mg |
1501-10 |
 BIOVISION, INC. |
More Info
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| A-769662 |
Cell-permeable. A potent AMPK activator. Directly stimulates partially purified rat liver AMPK (EC?? = 0.8 µM) and inhibits fatty acid synthesis in primary rat hepatocytes (IC5?? = 3.2 µM). |
5 mg |
1719-5 |
 BIOVISION, INC. |
More Info
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| A77 1726 |
Physiologically active metabolite of the immunosuppressive drug leflunomide (Cat. No.1972-10, 50). Inhibits the activity of dihydrorotate dehydrogenase and of protein tyrosine kinases. Blocks TNF-mediated NF-kappaB activation in a dose- and time-d... |
5 mg |
1973-5 |
 BIOVISION, INC. |
More Info
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| A77 1726 |
Physiologically active metabolite of the immunosuppressive drug leflunomide (Cat. No.1972-10, 50). Inhibits the activity of dihydrorotate dehydrogenase and of protein tyrosine kinases. Blocks TNF-mediated NF-kappaB activation in a dose- and time-d... |
25 mg |
1973-25 |
 BIOVISION, INC. |
More Info
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| A-71623 |
CCK1 Receptor Agonist |
1 mg |
2411/1 |
 R&D SYSTEMS, INC. |
More Info
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| A23187 |
Purity: >98%. A23187 (Calcimycin). Widely Used Ca2+ Ionophore. A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic fromStreptomyces chartreusensis. It is used to increase intrac... |
1 mg |
A-600 |
 ALOMONE LABS |
More Info
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| A23187 |
Purity: >98%. A23187 (Calcimycin). Widely Used Ca2+ Ionophore. A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic fromStreptomyces chartreusensis. It is used to increase intrac... |
10 x 1 mg |
A-600 |
 ALOMONE LABS |
More Info
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| A23187 |
Purity: >98%. A23187 (Calcimycin). Widely Used Ca2+ Ionophore. A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic fromStreptomyces chartreusensis. It is used to increase intrac... |
5 mg |
A-600 |
 ALOMONE LABS |
More Info
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| A23187 |
Purity: >98%. A23187 (Calcimycin). Widely Used Ca2+ Ionophore. A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic fromStreptomyces chartreusensis. It is used to increase intrac... |
5 x 5 mg |
A-600 |
 ALOMONE LABS |
More Info
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| A23187 |
Purity: >98%. A23187 (Calcimycin). Widely Used Ca2+ Ionophore. A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic fromStreptomyces chartreusensis. It is used to increase intrac... |
10 mg |
A-600 |
 ALOMONE LABS |
More Info
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| A23187 |
Purity: >98%. A23187, Calcimycin, Ca2+ Ionophore A23187, A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic from Streptomyces chartreusensis. It is used to increase intracellul... |
10 x 1 mg |
A-600 |
 ALOMONE LABS |
More Info
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| A23187 |
Purity: >98%. A23187, Calcimycin, Ca2+ Ionophore A23187, A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic from Streptomyces chartreusensis. It is used to increase intracellul... |
1 mg |
A-600 |
 ALOMONE LABS |
More Info
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| A23187 |
Purity: >98%. A23187, Calcimycin, Ca2+ Ionophore A23187, A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic from Streptomyces chartreusensis. It is used to increase intracellul... |
5 mg |
A-600 |
 ALOMONE LABS |
More Info
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| A23187 |
Purity: >98%. A23187, Calcimycin, Ca2+ Ionophore A23187, A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic from Streptomyces chartreusensis. It is used to increase intracellul... |
5 x 5 mg |
A-600 |
 ALOMONE LABS |
More Info
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| A23187 |
Purity: >98%. A23187, Calcimycin, Ca2+ Ionophore A23187, A23187 is a mobile-carrier Ca2+ ionophore (allows Ca2+ ions to cross cell membranes) originally isolated as an antibiotic from Streptomyces chartreusensis. It is used to increase intracellul... |
10 mg |
A-600 |
 ALOMONE LABS |
More Info
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| A-803467 |
Purity: >99%. A-803467. A Potent and Selective Inhibitor of the TTX-Resistant Na\v\1.8 Channel.The TTX-resistant, Na\v\1.8 channel is expressed almost exclusively in the PNS and has been shown to mediate most of the well documented TTX-resistant c... |
5 mg |
A-105 |
 ALOMONE LABS |
More Info
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| A-803467 |
Purity: >99%. A-803467. A Potent and Selective Inhibitor of the TTX-Resistant Na\v\1.8 Channel.The TTX-resistant, Na\v\1.8 channel is expressed almost exclusively in the PNS and has been shown to mediate most of the well documented TTX-resistant c... |
10 mg |
A-105 |
 ALOMONE LABS |
More Info
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| A-803467 |
Purity: >99%. A-803467. A Potent and Selective Inhibitor of the TTX-Resistant Na\v\1.8 Channel.The TTX-resistant, Na\v\1.8 channel is expressed almost exclusively in the PNS and has been shown to mediate most of the well documented TTX-resistant c... |
25 mg |
A-105 |
 ALOMONE LABS |
More Info
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| A-803467 |
Purity: >99%. A-803467. A Potent and Selective Inhibitor of the TTX-Resistant Na\v\1.8 Channel.The TTX-resistant, Na\v\1.8 channel is expressed almost exclusively in the PNS and has been shown to mediate most of the well documented TTX-resistant c... |
50 mg |
A-105 |
 ALOMONE LABS |
More Info
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| A-803467 |
Purity: >99%. A-803467. A Potent and Selective Inhibitor of the TTX-Resistant Na\v\1.8 Channel.The TTX-resistant, Na\v\1.8 channel is expressed almost exclusively in the PNS and has been shown to mediate most of the well documented TTX-resistant c... |
100 mg |
A-105 |
 ALOMONE LABS |
More Info
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| A-71623 |
Potent CCK1 agonist (IC50 = 3.7 nM) with 1200-fold selectivity over the CCK2 receptor. Suppresses food intake following central or peripheral administration. Minimum Purity: > 98% |
1mg |
2411 |
 TOCRIS BIOSCIENCE |
More Info
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| A-769662 |
MW: 360.39 Da. CAS number: [8444499-71-4]. Formula: C20H12N2O3S. Solubility: Soluble in DMSO at 33 mg/mL; soluble in ethanol at 5 mg/mL with slight warming; very poorly soluble in water; maximum solubility in plain water is estimated to be about 5... |
50 mg |
orb61202 |
 BIORBYT LTD. |
More Info
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| A77 1726 |
Molecular Weight: 270.2. White solid. Packaged under inert gas. |
5 mg |
100128-5MG |
 EMD MILLIPORE |
More Info
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| AA2 |
n/a |
n/a |
n/a |
 NIH AIDS RESEARCH & REFERENCE REAGENT PROGRAM |
More Info
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| AA 2414 |
Prostanoid Receptor Antagonist |
10 mg |
3025/10 |
 R&D SYSTEMS, INC. |
More Info
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| AA 2414 |
Prostanoid Receptor Antagonist |
50 mg |
3025/50 |
 R&D SYSTEMS, INC. |
More Info
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| AA 29504 |
GABA-A Receptor Modulator |
10 mg |
3972/10 |
 R&D SYSTEMS, INC. |
More Info
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| AA 29504 |
GABA-A Receptor Modulator |
50 mg |
3972/50 |
 R&D SYSTEMS, INC. |
More Info
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| Aa1 |
Purity: >98%. Aa1. A Novel Blocker of Shaker-B and IA K+ Channels. Native Aa1 was originally isolated from Androctonus australis scorpion venom. Aa1 is a recombinant peptide expressed in and extracted from E. coli and purified to homogeneity. Nati... |
5 µg |
RTA-400 |
 ALOMONE LABS |
More Info
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| Aa1 |
Purity: >98%. Aa1. A Novel Blocker of Shaker-B and IA K+ Channels. Native Aa1 was originally isolated from Androctonus australis scorpion venom. Aa1 is a recombinant peptide expressed in and extracted from E. coli and purified to homogeneity. Nati... |
5 x 5 µg |
RTA-400 |
 ALOMONE LABS |
More Info
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| Aa1 |
Purity: >98%. Aa1. A Novel Blocker of Shaker-B and IA K+ Channels. Native Aa1 was originally isolated from Androctonus australis scorpion venom. Aa1 is a recombinant peptide expressed in and extracted from E. coli and purified to homogeneity. Nati... |
10 µg |
RTA-400 |
 ALOMONE LABS |
More Info
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| Aa1 |
Purity: >98%. Aa1. A Novel Blocker of Shaker-B and IA K+ Channels. Native Aa1 was originally isolated from Androctonus australis scorpion venom. Aa1 is a recombinant peptide expressed in and extracted from E. coli and purified to homogeneity. Nati... |
5 x 10 µg |
RTA-400 |
 ALOMONE LABS |
More Info
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| Aa1 |
Purity: >98%. Aa1. A Novel Blocker of Shaker-B and IA K+ Channels. Native Aa1 was originally isolated from Androctonus australis scorpion venom. Aa1 is a recombinant peptide expressed in and extracted from E. coli and purified to homogeneity. Nati... |
0.1 mg |
RTA-400 |
 ALOMONE LABS |
More Info
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| AA 2414 |
Thromboxane A2 (TP) receptor antagonist. Antiasthmatic agent; inhibits platelet aggregation and bronchoconstriction induced by a TXA2 mimetic in guinea pigs. Minimum Purity: > 98% |
10mg |
3025 |
 TOCRIS BIOSCIENCE |
More Info
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| AA 2414 |
Thromboxane A2 (TP) receptor antagonist. Antiasthmatic agent; inhibits platelet aggregation and bronchoconstriction induced by a TXA2 mimetic in guinea pigs. Minimum Purity: > 98% |
50mg |
3025 |
 TOCRIS BIOSCIENCE |
More Info
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| AA 29504 |
Positive allosteric modulator of GABAA receptors. Modulates both alpha4beta3delta-containi ng extrasynaptic receptors and alpha1beta3gamma2S-contai ning receptors in Xenopus oocytes, displaying a stronger modulatory effect at the former. Reduces mot... |
10mg |
3972 |
 TOCRIS BIOSCIENCE |
More Info
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| AA 29504 |
Positive allosteric modulator of GABAA receptors. Modulates both alpha4beta3delta-containi ng extrasynaptic receptors and alpha1beta3gamma2S-contai ning receptors in Xenopus oocytes, displaying a stronger modulatory effect at the former. Reduces mot... |
50mg |
3972 |
 TOCRIS BIOSCIENCE |
More Info
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| AACOCF3 |
Phospholipase Inhibitor |
25 mg |
1462/25 |
 R&D SYSTEMS, INC. |
More Info
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| AACOCF3 |
Phospholipase Inhibitor |
5 mg |
1462/5 |
 R&D SYSTEMS, INC. |
More Info
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| AACOCF3 |
Inhibitor of cytosolic (85 kDa) phospholipase A2. Also inhibits fatty acid amide hydrolase (FAAH, anandamide amidase) in vitro. Minimum Purity: > 98% |
25mg |
1462 |
 TOCRIS BIOSCIENCE |
More Info
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| AACOCF3 |
Inhibitor of cytosolic (85 kDa) phospholipase A2. Also inhibits fatty acid amide hydrolase (FAAH, anandamide amidase) in vitro. Minimum Purity: > 98% |
5mg |
1462 |
 TOCRIS BIOSCIENCE |
More Info
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| 17-AAG |
17-AAG Purity is greater than 99%. |
250 mg |
orb60994 |
 BIORBYT LTD. |
More Info
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| 17-AAG |
Antimicrobial. CAS No.: 75747-14-7 |
n/a |
n/a |
 TOKU-E |
More Info
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| 17-AAG |
A semi-synthetic derivative of Geldanamycin (Cat. No. 1564-1,5) that displays greater stability and lower in vivo toxicity compared to Geldanamycin. Binds to Heat shock protein 90 (Hsp90) (EC?? = 7.2 µM) in a manner similar to geldanamycin. ... |
1 mg |
1774-1 |
 BIOVISION, INC. |
More Info
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| 17-AAG |
A semi-synthetic derivative of Geldanamycin (Cat. No. 1564-1,5) that displays greater stability and lower in vivo toxicity compared to Geldanamycin. Binds to Heat shock protein 90 (Hsp90) (EC?? = 7.2 µM) in a manner similar to geldanamycin. ... |
5 mg |
1774-5 |
 BIOVISION, INC. |
More Info
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| 17-AAG |
HSP90 Inhibitor |
1 mg |
1515/1 |
 R&D SYSTEMS, INC. |
More Info
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| 17-AAG |
Purity: >99%. 17-AAG, An Anticancer Antibiotic. 17-AAG is a less toxic and more stable derivative of the antibiotic Geldanamycin. It binds to Hsp90 and regulates its function. Hsp90 regulates the physiology of cells exposed to environmental stress... |
0.1 mg |
A-580 |
 ALOMONE LABS |
More Info
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| 17-AAG |
Purity: >99%. 17-AAG, An Anticancer Antibiotic. 17-AAG is a less toxic and more stable derivative of the antibiotic Geldanamycin. It binds to Hsp90 and regulates its function. Hsp90 regulates the physiology of cells exposed to environmental stress... |
5 x 0.1 mg |
A-580 |
 ALOMONE LABS |
More Info
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| 17-AAG |
Inhibitor of heat shock protein 90 (Hsp90) chaperone activity, and an analog of geldanamycin (Cat. No. 1368). Subsequently inhibits the activity of oncogenic proteins such as p185erbB-2 (IC50 = 31 nM), N-ras, Ki-ras and c-Akt. Antitumor in vivo. M... |
1mg |
1515 |
 TOCRIS BIOSCIENCE |
More Info
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