sb-431542

346  

SB-431542
HY-10431 100mg
EUR 821
Sb 431542
20-abx182645
  • EUR 1497.00
  • EUR 370.00
  • 100 mg
  • 10 mg
  • Shipped within 1-2 weeks.
SB 431542
A8249-10 10 mg
EUR 139
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.
SB 431542
A8249-5.1 10 mM (in 1mL DMSO)
EUR 166
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.
SB 431542
A8249-50 50 mg
EUR 431
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.
SB 431542
A8249-S Evaluation Sample
EUR 81
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.
SB-431542
1674-1
EUR 169
SB-431542
1674-5
EUR 446
SB 431542, > 98%
BC261-005 5 mg
EUR 232
SB 431542, > 98%
BC261-010 10 mg
EUR 313
SB 431542, > 98%
BC261-050 50 mg
EUR 928
EZSolution? SB-431542
1872-1
EUR 158
EZSolution? SB-431542, Sterile-Filtered
1992-1
EUR 272
SB 202474
C4949-1 1 mg
EUR 209
Description: SB 202474 is a structural analog of SB 202190 and SB 203580 that is used as a negative control in researches of p38 inhibition. SB 202190 and SB 203580 are potent and selective inhibitors of the MAP kinases p38? and p38? [1][2][3].
SB-590885
B1708-25
EUR 544
SB-590885
B1708-5
EUR 175
SB-415286
B1954-25
EUR 756
SB-415286
B1954-5
EUR 229
SB-242235
B2273-25
EUR 512
SB-242235
B2273-5
EUR 175
SB-204490
B2507-1
EUR 131
SB-204490
B2507-5
EUR 349
SB-297006
B2589-25
EUR 457
SB-297006
B2589-5
EUR 153
SB 706375
B5677-10 10 mg
EUR 373
SB 706375
B5677-50 50 mg
EUR 1363
SB 611812
B5678-10 10 mg
EUR 373
SB 611812
B5678-50 50 mg
EUR 1363
SB 204990
B5782-1 1 mg
EUR 112
SB 204990
B5782-10 10 mg
EUR 335
SB 204990
B5782-5 5 mg
EUR 224
SB 204741
B6708-10 10 mg
EUR 302
SB 204741
B6708-50 50 mg
EUR 1114
SB 228357
B6709-10 10 mg
EUR 366
SB 228357
B6709-50 50 mg
EUR 1379
SB 218795
B6710-10 10 mg
EUR 383
SB 218795
B6710-50 50 mg
EUR 1455
SB 221284
B6713-10 10 mg
EUR 324
SB 221284
B6713-50 50 mg
EUR 1211
SB 205384
B6770-10 10 mg
EUR 366
Description: SB-205384 is a selective and positive GABAA receptor modulator with EC50 values of 280, 695 and 730 nM on ?6, ?3 and ?5-subunit-containing receptors, respectively [1].
SB 205384
B6770-50 50 mg
EUR 1379
Description: SB-205384 is a selective and positive GABAA receptor modulator with EC50 values of 280, 695 and 730 nM on ?6, ?3 and ?5-subunit-containing receptors, respectively [1].
SB 366791
B6804-10 10 mg
EUR 239
SB 366791
B6804-5.1 10 mM (in 1mL DMSO)
EUR 142
SB 366791
B6804-50 50 mg
EUR 853
SB-334867
B1281-10 10 mg
EUR 154
Description: SB-334867 is a selective antagonist of orexin-1 receptor [1].Orexin-A and orexin-B are two peptides isolated from rat hypothalamus. They are involved in some physiological functions such as the control of feeding, energy metabolism and regulation of the sleep-wake cycle.
SB-334867
B1281-25 25 mg
EUR 270
Description: SB-334867 is a selective antagonist of orexin-1 receptor [1].Orexin-A and orexin-B are two peptides isolated from rat hypothalamus. They are involved in some physiological functions such as the control of feeding, energy metabolism and regulation of the sleep-wake cycle.
SB-334867
B1281-5 5 mg
EUR 110
Description: SB-334867 is a selective antagonist of orexin-1 receptor [1].Orexin-A and orexin-B are two peptides isolated from rat hypothalamus. They are involved in some physiological functions such as the control of feeding, energy metabolism and regulation of the sleep-wake cycle.
SB-334867
B1281-5.1 10 mM (in 1mL DMSO)
EUR 119
Description: SB-334867 is a selective antagonist of orexin-1 receptor [1].Orexin-A and orexin-B are two peptides isolated from rat hypothalamus. They are involved in some physiological functions such as the control of feeding, energy metabolism and regulation of the sleep-wake cycle.
SB-334867
B1281-50 50 mg
EUR 402
Description: SB-334867 is a selective antagonist of orexin-1 receptor [1].Orexin-A and orexin-B are two peptides isolated from rat hypothalamus. They are involved in some physiological functions such as the control of feeding, energy metabolism and regulation of the sleep-wake cycle.
SB-3CT
B4792-100 100 mg
EUR 827
Description: SB-3CT is a potent and selective inhibitor of gelatinases with Ki values of 13.9 and 600 nM for MMP-2 and MMP-9, respectively. Gelatinases A (MMP-2) and B (MMP-9) belong to matrix metalloproteinases family and are involved in tumor metastasis and angiogenesis by hydrolyzing extracellular matrix.
SB-3CT
B4792-25 25 mg
EUR 444
Description: SB-3CT is a potent and selective inhibitor of gelatinases with Ki values of 13.9 and 600 nM for MMP-2 and MMP-9, respectively. Gelatinases A (MMP-2) and B (MMP-9) belong to matrix metalloproteinases family and are involved in tumor metastasis and angiogenesis by hydrolyzing extracellular matrix.
SB-3CT
B4792-5 5 mg
EUR 200
Description: SB-3CT is a potent and selective inhibitor of gelatinases with Ki values of 13.9 and 600 nM for MMP-2 and MMP-9, respectively. Gelatinases A (MMP-2) and B (MMP-9) belong to matrix metalloproteinases family and are involved in tumor metastasis and angiogenesis by hydrolyzing extracellular matrix.
SB 706504
B4937-10 10 mg
EUR 373
SB 706504
B4937-50 50 mg
EUR 1413
SB 204070
B5105-10 10 mg
EUR 405
SB 265610
B5333-1 1 mg
EUR 160
Description: SB 265610 is a potent CXCR2 antagonist that inhibits CINC-1-mediated Ca2+ mobilization with IC50 value of 3.4nM [1] [2]. CXCR2 is an integral membrane protein that specifically binds and responds to cytokines of the CXC chemokine family.
SB 265610
B5333-10 10 mg
EUR 303
Description: SB 265610 is a potent CXCR2 antagonist that inhibits CINC-1-mediated Ca2+ mobilization with IC50 value of 3.4nM [1] [2]. CXCR2 is an integral membrane protein that specifically binds and responds to cytokines of the CXC chemokine family.
SB 265610
B5333-5 5 mg
EUR 196
Description: SB 265610 is a potent CXCR2 antagonist that inhibits CINC-1-mediated Ca2+ mobilization with IC50 value of 3.4nM [1] [2]. CXCR2 is an integral membrane protein that specifically binds and responds to cytokines of the CXC chemokine family.
SB 242084
B5348-10 10 mg
EUR 267
SB 242084
B5348-50 50 mg
EUR 1044
SB 328437
B5467-10 10 mg
EUR 334
SB 328437
B5467-50 50 mg
EUR 1243
SB 297006
B5542-10 10 mg
EUR 224
SB 297006
B5542-25 25 mg
EUR 441
SB 297006
B5542-5 5 mg
EUR 154
SB 699551
B7308-10 10 mg
EUR 389
SB 699551
B7308-50 50 mg
EUR 1476
SB 452533
B7335-10 10 mg
EUR 308
SB 452533
B7335-50 50 mg
EUR 1136
SB 657510
B7432-10 10 mg
EUR 383
SB 657510
B7432-50 50 mg
EUR 1439
SB 268262
B7645-10 10 mg
EUR 431
SB 268262
B7645-50 50 mg
EUR 1656
SB 225002
B8200-10 10 mg
EUR 131
Description: SB 225002 is a potent and selective CXCR2 chemokine receptor antagonist with IC50 value of 22nM [1].CXCR2 is a member of the G-protein-coupled receptor family, which is responsible for neutrophil chemotaxis and margination induced by IL-8 [1].
SB 225002
B8200-25 25 mg
EUR 224
Description: SB 225002 is a potent and selective CXCR2 chemokine receptor antagonist with IC50 value of 22nM [1].CXCR2 is a member of the G-protein-coupled receptor family, which is responsible for neutrophil chemotaxis and margination induced by IL-8 [1].
SB 225002
B8200-5 5 mg
EUR 108
Description: SB 225002 is a potent and selective CXCR2 chemokine receptor antagonist with IC50 value of 22nM [1].CXCR2 is a member of the G-protein-coupled receptor family, which is responsible for neutrophil chemotaxis and margination induced by IL-8 [1].
SB 225002
B8200-5.1 10 mM (in 1mL DMSO)
EUR 125
Description: SB 225002 is a potent and selective CXCR2 chemokine receptor antagonist with IC50 value of 22nM [1].CXCR2 is a member of the G-protein-coupled receptor family, which is responsible for neutrophil chemotaxis and margination induced by IL-8 [1].
SB 225002
B8200-50 50 mg
EUR 340
Description: SB 225002 is a potent and selective CXCR2 chemokine receptor antagonist with IC50 value of 22nM [1].CXCR2 is a member of the G-protein-coupled receptor family, which is responsible for neutrophil chemotaxis and margination induced by IL-8 [1].
SB 218078
C3012-1 1 mg
EUR 209
Description: Targets:Chk1, cdc2 and PKCIC50:15, 250 and 1000 nM for Chk1, cdc2 and PKC respectivelySB 218078 is a potent inhibitor of checkpoint kinase 1, with the IC50 values of 15, 250 and 1000 nM for Chk1, cdc2 and PKC, respectively.
SB 216763
E1KS1075 5 mg
EUR 206
SB 203580
E1KS1076 25 mg
EUR 284
SB 202190
E1KS1077 25 mg
EUR 284
SB 525334
E1KS1476 5mg
EUR 325
SB-408124
E1KS1545 5mg
EUR 325
SB 743921
E1KS2182 10mg
EUR 1504