Name | Description | Size | Catalog # | Supplier | |
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10074-A4 | 10074-A4 is a c-Myc binding compound that associates with c-Myc370-409 and… | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg, 500 mg | orb1297969 |
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1588-A4 | Purity >98% (HPLC). 1588-A4 is an intermediate of ARS-1620 which is an atr… | 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | orb1219512 |
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1A-116 | 1A-116 is a specific Rac1 inhibitor. MW: 307.32 | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg | orb1308731 |
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360A | Purity > 98%. MW: 449.5 | 5 mg, 10 mg, 50 mg | orb1182536 |
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A 1070722 | Purity > 98%. MW: 362.31 | 5 mg, 10 mg, 50 mg, 100 mg | orb1180501 |
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A 1120 | A 1120 is a nonretinoid retinol-binding protein 4 (RBP4) antagonist (Ki: 8… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg | orb1310034 |
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A 286982 | Purity >98% (HPLC). A 286982 is an inhibitor that blocks the integrin-liga… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg | orb1218229 |
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A 425619 | Purity >98% (HPLC). A 425619 is a potent TRPV1 antagonistsystemic administ… | 5 mg, 10 mg, 25 mg | orb1219945 |
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A 438079 | MW: 306.15 | 100 mg, 250 mg, 1 g | orb654683 |
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A 769662 | Purity ≥99% (HPLC). MW: 360.4 | 5 mg, 25 mg | orb1467493 |
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A 77-01 | A 77-01 is a potent inhibitor of TGF-(beta) type I receptor superfamily ac… | 2 mg, 5 mg, 10 mg, 25 mg | orb1306488 |
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A 784168 | Purity > 98%. MW: 479.4 | 10 mg, 25 mg, 50 mg, 100 mg | orb1179313 |
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A 804598 | MW: 315.3718 | 100 mg, 250 mg, 1 g | orb16594 |
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A 83-01 | Purity ≥98%. MW: 421.52 | 5 mg, 25 mg, 100 mg | orb610367 |
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A 839977 | Purity > 98%. MW: 413.26 | 10 mg, 25 mg, 50 mg, 100 mg | orb1179821 |
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A 922500 | A922500 is an inhibitor for human and mouse DGAT-1 with IC50 of 7 nM and 2… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | orb1300832 |
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A11 | Purity > 95% by hplc. ANXA1-EphA2 interaction blocker. | 1 mg | orb1140473 |
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A1120 | MW: 392.3782 | 100 mg, 250 mg, 1 g | orb692106 |
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A1155463 | MW: 669.7881 | 100 mg, 250 mg, 1 g | orb385568 |
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A-1155463 | A-1155463, a highly potent and selective BCL-XL inhibitor, shows picomolar… | 2 mg, 5 mg, 10 mg, 25 mg | orb1300502 |
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A-1165442 | Purity > 98%. MW: 431.86 | 1 mg, 5 mg, 10 mg, 50 mg | orb1179629 |
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A-1210477 | A-1210477 is an effective and specific MCL-1 and Bcl-2 inhibitor (Ki / IC5… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | orb1305241 |
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A-1331852 | A-1331852 is a potent and selectiveBCL-XL inhibitor and may be useful in t… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | orb1300501 |
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A1874 | A1874 is a nutlin-based and BRD4-degrading PROTAC which induces BRD4 degra… | 1 mg, 5 mg | orb1301788 |
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A1874 | Purity >98% (HPLC). A1874 (A-1874) is a nutlin-based and BRD4-degrading PR… | 2 mg, 5 mg, 10 mg, 25 mg | orb1225722 |
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A-196 | Purity > 98%. MW: 359.2 | 5 mg, 25 mg | orb636770 |
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A-196 | n/a | 100 mg, 250 mg, 1 g | orb413193 |
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A-205804 | A-205804 is a specific and effective inhibitor of E-selectin( IC50=20 nM )… | 2 mg, 5 mg, 10 mg, 25 mg, 100 mg | orb1305886 |
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A-23187 | Purity > 98%. MW: 523.62 | 5 mg, 25 mg, 50 mg | orb340508 |
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A2793 | MW: 265.69 | 100 mg, 250 mg, 1 g | orb783559 |
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A286982 | A286982 is an inhibitor that blocks the integrin-ligand interaction betwee… | 100 mg, 250 mg, 1 g | orb746361 |
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A-286982 | A 286982 is an inhibitor that blocks the integrin-ligand interaction betwe… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg | orb1306203 |
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A-317491 | Purity >98% (HPLC). A-317491 is a non-nucleotide P2X3 ( Ki: 22 nM) and P2X… | 5 mg, 10 mg, 50 mg | orb1218002 |
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A-366 | Potent and selective G9a / GLP histone lysine methyltransferase inhibitor… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | orb1303986 |
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A-381393 | MW: 320.431 | 100 mg, 250 mg, 1 g | orb573240 |
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A-385358 | Purity > 98%. MW: 639.83 | 5 mg, 10 mg, 50 mg | orb1182059 |
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A-395 | Purity > 98%. MW: 486.65 | 5 mg, 10 mg, 50 mg, 100 mg | orb1183092 |
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A40926 | n/a | 100 mg, 250 mg, 1 g | orb1089610 |
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A419259 | Purity > 98%. MW: 482.6 | 10 mg, 25 mg, 100 mg | orb1182633 |
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A-420983 | MW: 593.72186 | 100 mg | orb573446 |
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A4250 | MW: 740.929 | 100 mg, 250 mg, 1 g | orb1473162 |
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A-438079 | Purity > 98%. MW: 342.61 | 5 mg, 25 mg | orb1147159 |
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A-443654 | Purity > 98%. MW: 397.5 | 2 mg, 5 mg, 10 mg | orb1183541 |
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A-484954 | MW: 289.29 | 100 mg, 250 mg, 1 g | orb572970 |
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A-485 | A-485 is a potent and selective catalytic p300 / CBP inhibitor(IC50s of 9.… | 1 mg, 5 mg, 10 mg, 50 mg, 100 mg | orb1308704 |
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A-582941 | Purity > 98%. MW: 280.37 | 10 mg, 25 mg, 50 mg | orb1182852 |
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A66 | MW: 393.5268 | 100 mg, 250 mg, 1000 mg | orb181355 |
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A66 | Purity > 98%. MW: 393.53 | 10 mg | orb1102074 |
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A-674563 | Purity > 98%. | 5 mg, 50 mg | orb762682 |
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A-674563 | Purity >98% (HPLC). A-674563 is a potent, selective and orally available A… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | orb1224692 |
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A-69412 | Purity > 98%. MW: 170.17 | 5 mg, 10 mg, 50 mg | orb1180893 |
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A-740003 | MW: 474.57 | 100 mg, 250 mg, 1000 mg | orb181189 |
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A-769662 | A-769662 is an effective, reversible AMPK activator(EC50=0.8 µM). MW… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | orb1305442 |
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A-769662 | Purity ≥98%. MW: 360.39 | 5 mg, 10 mg | orb419390 |
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A-769662 | Purity > 98%. MW: 360.39 | 20 mg | orb1101957 |
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A77 1726 | Purity > 98%. MW: 270.21 | 5 mg, 25 mg | orb340365 |
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A-770041 | Purity > 98%. MW: 621.75 | 5 mg, 10 mg, 50 mg | orb1183540 |
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A77-01 | MW: 286.3306 | 100 mg, 250 mg, 1000 mg | orb304081 |
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A-779 | A-779 is a peptide antagonist of the Mas receptor, also known as the angio… | 100 mg, 250 mg, 1 g | orb525696 |
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A803467 | Purity > 98%. | 10 mg | orb762702 |
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A-803467 | MW: 357.7876 | 100 mg, 250 mg, 1 g | orb180777 |
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A-803467 | Purity > 98%. MW: 357.8 | 10 mg, 50 mg | orb545812 |
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A-804598 | Purity >98% (HPLC). A-804598 is a competitive and selective P2X7 receptor… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | orb1223426 |
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A83 01 | Purity ≥98% (HPLC). MW: 421.5 | 5 mg, 25 mg | orb1467557 |
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A83-01 | Purity > 98%. MW: 421.5 | 5 mg, 25 mg | orb545883 |
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A-836339 | A-836339 acts as a potent cannabinoid receptor full agonist which has a hi… | 1 mg, 5 mg, 10 mg, 50 mg, 100 mg, 200 mg | orb1299873 |
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A-836339 | Purity >98% (HPLC). A-836339 (A836339) is a potent and selective cannabino… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg | orb1223516 |
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A-841720 | Purity > 98%. MW: 343.45 | 10 mg, 25 mg, 50 mg | orb1182733 |
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A-867744 | Purity >98% (HPLC). A-867744 is an effective and selective type II positiv… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg | orb1219204 |
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A-889425 | Purity > 98%. MW: 425.425 | 5 mg, 10 mg, 25 mg | orb1182876 |
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A-893 | Purity > 98%. MW: 577.54 | 1 mg, 5 mg, 10 mg | orb1180044 |
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A922500 | Purity >98% (HPLC). A922500 is an inhibitor for human and mouse DGAT-1 wit… | 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | orb1222966 |
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A939572 | A939572 is stearoyl-CoA desaturase1 (SCD1) inhibitor with IC50 values of <… | 2 mg, 5 mg, 10 mg, 50 mg, 100 mg | orb1302794 |
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A-966492 | MW: 324.35 | 100 mg, 250 mg, 1000 mg | orb180912 |
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A-967079 | Purity > 98%. MW: 207.25 | 5 mg, 25 mg, 50 mg | orb340181 |
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A-967079 | Purity >98% (HPLC). A potent, selective TRPA1 channel blocker with IC50 of… | 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | orb1226887 |
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A-9758 | Purity > 98%. MW: 527.36 | 5 mg, 10 mg, 50 mg | orb1181128 |
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A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 10 mg | A-345 |
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A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 25 mg | A-345 |
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A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 5 mg | A-345 |
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A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 50 mg | A-345 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 1 mg | A-360 |
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A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 10 mg | A-360 |
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A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 25 mg | A-360 |
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A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 5 mg | A-360 |
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A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 1 mg | A-600 |
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A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 10 mg | A-600 |
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A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 10 x 1 mg | A-600 |
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A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 5 mg | A-600 |
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A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 5 x 5 mg | A-600 |
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A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 10 mg | A-420 |
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A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 100 mg | A-420 |
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A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 25 mg | A-420 |
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A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 50 mg | A-420 |
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