PPACK Dihydrochloride
Contact us: [email protected]
H89 Dihydrochloride |
20-abx076747 |
Abbexa |
|
|
|
MPP dihydrochloride |
B6910-10 |
ApexBio |
10 mg |
EUR 381.6 |
MPP dihydrochloride |
B6910-50 |
ApexBio |
50 mg |
EUR 1413.6 |
TMB dihydrochloride |
TB0514 |
Bio Basic |
1g |
EUR 85.06 |
|
IT1t dihydrochloride |
B5650-10 |
ApexBio |
10 mg |
EUR 385.2 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
IT1t dihydrochloride |
B5650-100 |
ApexBio |
100 mg |
EUR 2100 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
IT1t dihydrochloride |
B5650-25 |
ApexBio |
25 mg |
EUR 710.4 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
IT1t dihydrochloride |
B5650-5 |
ApexBio |
5 mg |
EUR 243.6 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
IT1t dihydrochloride |
B5650-5.1 |
ApexBio |
10 mM (in 1mL DMSO) |
EUR 261.6 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
IT1t dihydrochloride |
B5650-50 |
ApexBio |
50 mg |
EUR 1232.4 |
Description: IT1t dihydrochloride is a potent antagonist of CXCR4 with IC50 value of 8.0 nM [1]. C-X-C chemokine receptor type 4 (CXCR4) is an ?-chemokine receptor for chemokine CXCL12. |
1400W dihydrochloride |
2055-25 |
Biovision |
each |
EUR 405.6 |
1400W dihydrochloride |
2055-5 |
Biovision |
each |
EUR 151.2 |
DMPQ Dihydrochloride |
20-abx076714 |
Abbexa |
|
|
|
DMPQ dihydrochloride |
B6642-10 |
ApexBio |
10 mg |
EUR 223.2 |
DMPQ dihydrochloride |
B6642-5 |
ApexBio |
5 mg |
EUR 184.8 |
GNTI dihydrochloride |
B6669-10 |
ApexBio |
10 mg |
EUR 459.6 |
GNTI dihydrochloride |
B6669-50 |
ApexBio |
50 mg |
EUR 1746 |
1400W dihydrochloride |
B6730-10 |
ApexBio |
10 mg |
EUR 170.4 |
Description: 1400W dihydrochloride is a potent and selective inhibitor of inducible nitric oxide synthase with Kd value of 7 nM [1]. Inducible nitric oxide synthase (iNOS) is an enzyme catalyzing the production of nitric oxide (NO) and is involved in immune response. |
1400W dihydrochloride |
B6730-100 |
ApexBio |
100 mg |
EUR 873.6 |
Description: 1400W dihydrochloride is a potent and selective inhibitor of inducible nitric oxide synthase with Kd value of 7 nM [1]. Inducible nitric oxide synthase (iNOS) is an enzyme catalyzing the production of nitric oxide (NO) and is involved in immune response. |
1400W dihydrochloride |
B6730-50 |
ApexBio |
50 mg |
EUR 525.6 |
Description: 1400W dihydrochloride is a potent and selective inhibitor of inducible nitric oxide synthase with Kd value of 7 nM [1]. Inducible nitric oxide synthase (iNOS) is an enzyme catalyzing the production of nitric oxide (NO) and is involved in immune response. |
GGACK Dihydrochloride |
1847-5 |
Biovision |
5 mg |
EUR 382.8 |
|
Description: A potent and irreversible inhibitor of Urokinase (uPA (IC??<1 µM), Factor VIIa, Factor IXa, Factor Xa, and trypsin. |
GGACK Dihydrochloride |
A2582-5 |
ApexBio |
5 mg |
EUR 282 |
Description: A potent and irreversible inhibitor of Urokinase (uPA (IC??<1 µM), Factor VIIa, Factor IXa, Factor Xa, and trypsin. |
GBR 12935 dihydrochloride |
B4661-10 |
ApexBio |
10 mg |
EUR 129.6 |
GBR 12935 dihydrochloride |
B4661-100 |
ApexBio |
100 mg |
EUR 296.4 |
GBR 12935 dihydrochloride |
B4661-50 |
ApexBio |
50 mg |
EUR 192 |
ETP 45835 dihydrochloride |
B4938-10 |
ApexBio |
10 mg |
EUR 428.4 |
ETP 45835 dihydrochloride |
B4938-50 |
ApexBio |
50 mg |
EUR 1608 |
AZ 10606120 dihydrochloride |
B5410-10 |
ApexBio |
10 mg |
EUR 408 |
Description: KD: 1.4 nM and 1.9 nM for human and rat P2X7 receptors, respectivleyThe P2X7 receptor has intriguing biophysical properties, activates a diverse range of cellular events and mediates a wide range of functional effects. |
AZ 10606120 dihydrochloride |
B5410-50 |
ApexBio |
50 mg |
EUR 1531.2 |
Description: KD: 1.4 nM and 1.9 nM for human and rat P2X7 receptors, respectivleyThe P2X7 receptor has intriguing biophysical properties, activates a diverse range of cellular events and mediates a wide range of functional effects. |
CP 99994 dihydrochloride |
B5422-10 |
ApexBio |
10 mg |
EUR 478.8 |
CP 99994 dihydrochloride |
B5422-50 |
ApexBio |
50 mg |
EUR 1824 |
SB 243213 dihydrochloride |
B5444-10 |
ApexBio |
10 mg |
EUR 486 |
SB 243213 dihydrochloride |
B5444-50 |
ApexBio |
50 mg |
EUR 1802.4 |
JNJ 5207852 dihydrochloride |
B5513-10 |
ApexBio |
10 mg |
EUR 289.2 |
JNJ 5207852 dihydrochloride |
B5513-5 |
ApexBio |
5 mg |
EUR 180 |
JNJ 5207852 dihydrochloride |
B5513-50 |
ApexBio |
50 mg |
EUR 1021.2 |
A 412997 dihydrochloride |
B5639-25 |
ApexBio |
25 mg |
EUR 642 |
Description: A 412997 dihydrochloride is a selective agonist of dopamine D4 receptor with Ki values of 7.9 and 12.1 nM for human and rat D4 receptors, respectively [1]. Dopamine D4 receptor is a G protein-coupled receptor and is activated by dopamine. |
A 412997 dihydrochloride |
B5639-5 |
ApexBio |
5 mg |
EUR 212.4 |
Description: A 412997 dihydrochloride is a selective agonist of dopamine D4 receptor with Ki values of 7.9 and 12.1 nM for human and rat D4 receptors, respectively [1]. Dopamine D4 receptor is a G protein-coupled receptor and is activated by dopamine. |
SA 4503 dihydrochloride |
B5778-10 |
ApexBio |
10 mg |
EUR 297.6 |
SA 4503 dihydrochloride |
B5778-5.1 |
ApexBio |
10 mM (in 1mL DMSO) |
EUR 343.2 |
SA 4503 dihydrochloride |
B5778-50 |
ApexBio |
50 mg |
EUR 1069.2 |
BMS 599626 dihydrochloride |
B5792-10 |
ApexBio |
10 mg |
EUR 642 |
Description: BMS 599626 dihydrochloride is a potent and selective inhibitor of EGFR and ErbB2 with IC50 values of 22 and 32 nM, respectively [1]. |
TC 1698 dihydrochloride |
B7089-10 |
ApexBio |
10 mg |
EUR 408 |
TC 1698 dihydrochloride |
B7089-50 |
ApexBio |
50 mg |
EUR 1531.2 |
JP 1302 dihydrochloride |
B7147-10 |
ApexBio |
10 mg |
EUR 466.8 |
JP 1302 dihydrochloride |
B7147-50 |
ApexBio |
50 mg |
EUR 1771.2 |
BYK 191023 dihydrochloride |
B7210-10 |
ApexBio |
10 mg |
EUR 297.6 |
Description: IC50: 86 nM for iNOSNO synthases are enzymes responsible for the generation of nitric oxide from the amino acid L-arginine. Once expressed the inducible NO synthase (iNOS) is active and produces ?M concentrations of NO over longer periods. |
BYK 191023 dihydrochloride |
B7210-5 |
ApexBio |
5 mg |
EUR 184.8 |
Description: IC50: 86 nM for iNOSNO synthases are enzymes responsible for the generation of nitric oxide from the amino acid L-arginine. Once expressed the inducible NO synthase (iNOS) is active and produces ?M concentrations of NO over longer periods. |
BYK 191023 dihydrochloride |
B7210-50 |
ApexBio |
50 mg |
EUR 999.6 |
Description: IC50: 86 nM for iNOSNO synthases are enzymes responsible for the generation of nitric oxide from the amino acid L-arginine. Once expressed the inducible NO synthase (iNOS) is active and produces ?M concentrations of NO over longer periods. |
ARL 17477 dihydrochloride |
B7363-10 |
ApexBio |
10 mg |
EUR 350.4 |
Description: ARL 17477 dihydrochloride is a selective and potent neuronal nitrogen oxide synthase (nNOS) inhibitor with IC50 values of 1 and 17?M for nNOS and endothelial NOS, respectively [1]. |
ARL 17477 dihydrochloride |
B7363-50 |
ApexBio |
50 mg |
EUR 1264.8 |
Description: ARL 17477 dihydrochloride is a selective and potent neuronal nitrogen oxide synthase (nNOS) inhibitor with IC50 values of 1 and 17?M for nNOS and endothelial NOS, respectively [1]. |
PD 168568 dihydrochloride |
B7420-10 |
ApexBio |
10 mg |
EUR 369.6 |
PD 168568 dihydrochloride |
B7420-50 |
ApexBio |
50 mg |
EUR 1363.2 |
A 943931 dihydrochloride |
B7495-10 |
ApexBio |
10 mg |
EUR 486 |
Description: A 943931, is an H4R (one of histamine receptor subtypes) antagonist [1] with high affinities to H4Rs of human (Ki = 5 nM), rat (Ki = 4 nM) and mouse (Kb = 6 nM) [2]. H4R is one of 4 known G-protein-coupled receptors of histamine for histamine to mediate its physiological functions [3]. |
A 943931 dihydrochloride |
B7495-50 |
ApexBio |
50 mg |
EUR 1802.4 |
Description: A 943931, is an H4R (one of histamine receptor subtypes) antagonist [1] with high affinities to H4Rs of human (Ki = 5 nM), rat (Ki = 4 nM) and mouse (Kb = 6 nM) [2]. H4R is one of 4 known G-protein-coupled receptors of histamine for histamine to mediate its physiological functions [3]. |
PG 01037 dihydrochloride |
B7524-10 |
ApexBio |
10 mg |
EUR 309.6 |
PG 01037 dihydrochloride |
B7524-25 |
ApexBio |
25 mg |
EUR 633.6 |
PG 01037 dihydrochloride |
B7524-5 |
ApexBio |
5 mg |
EUR 195.6 |
WAY 207024 dihydrochloride |
B7525-10 |
ApexBio |
10 mg |
EUR 576 |
Description: WAY 207024 dihydrochloride is a potent gonadotropin releasing hormone receptor (GnRH-R) antagonist with IC50 values of 12 and 71 nM for human and rat GnRH receptors, respectively [1]. |
WAY 208466 dihydrochloride |
B7531-10 |
ApexBio |
10 mg |
EUR 289.2 |
WAY 208466 dihydrochloride |
B7531-25 |
ApexBio |
25 mg |
EUR 582 |
WAY 208466 dihydrochloride |
B7531-5 |
ApexBio |
5 mg |
EUR 184.8 |
WAY 267464 dihydrochloride |
B7538-10 |
ApexBio |
10 mg |
EUR 556.8 |
JNJ 10181457 dihydrochloride |
B7567-10 |
ApexBio |
10 mg |
EUR 466.8 |
JNJ 10181457 dihydrochloride |
B7567-50 |
ApexBio |
50 mg |
EUR 1771.2 |
BMS 470539 dihydrochloride |
B7577-10 |
ApexBio |
10 mg |
EUR 544.8 |
Description: BMS 470539 dihydrochloride is a potent and selective melanocortin-1 (MC1) receptor agonist with IC50 of 120 nM [1]. The melanocortin-1 receptor (MC-1R) is a G protein-coupled receptor involved in blocking inflammation and augmenting skin pigmentation [1]. |
BMS 470539 dihydrochloride |
B7577-50 |
ApexBio |
50 mg |
EUR 2056.8 |
Description: BMS 470539 dihydrochloride is a potent and selective melanocortin-1 (MC1) receptor agonist with IC50 of 120 nM [1]. The melanocortin-1 receptor (MC-1R) is a G protein-coupled receptor involved in blocking inflammation and augmenting skin pigmentation [1]. |
PS 1145 dihydrochloride |
B7683-25 |
ApexBio |
25 mg |
EUR 428.4 |
PS 1145 dihydrochloride |
B7683-5 |
ApexBio |
5 mg |
EUR 164.4 |
A 331440 dihydrochloride |
B7698-10 |
ApexBio |
10 mg |
EUR 459.6 |
Description: A-331440 is described here instead of A-331440 dihydrochloride. A-331440 is an antagonist of non-imidazole histamine H3 receptor with an IC50 value of 22.7 nM for human cortex histamine H3 [1]. |
A 331440 dihydrochloride |
B7698-50 |
ApexBio |
50 mg |
EUR 1746 |
Description: A-331440 is described here instead of A-331440 dihydrochloride. A-331440 is an antagonist of non-imidazole histamine H3 receptor with an IC50 value of 22.7 nM for human cortex histamine H3 [1]. |
R 1485 dihydrochloride |
B7723-10 |
ApexBio |
10 mg |
EUR 466.8 |
R 1485 dihydrochloride |
B7723-50 |
ApexBio |
50 mg |
EUR 1771.2 |
DBM 1285 dihydrochloride |
B7748-10 |
ApexBio |
10 mg |
EUR 517.2 |
DBM 1285 dihydrochloride |
B7748-50 |
ApexBio |
50 mg |
EUR 1987.2 |
LDN 209929 dihydrochloride |
B7785-10 |
ApexBio |
10 mg |
EUR 466.8 |
Description: Target: haspin kinaseIC50: 55 nMLDN 209929 dihydrochloride is a selective and potent haspin kinase inhibitor with IC50 value of 55 nM [1]. LDN 209929 dihydrochloride displays 180-fold selectivity on haspin kinase over DYRK2 [1]. |
LDN 209929 dihydrochloride |
B7785-50 |
ApexBio |
50 mg |
EUR 1771.2 |
Description: Target: haspin kinaseIC50: 55 nMLDN 209929 dihydrochloride is a selective and potent haspin kinase inhibitor with IC50 value of 55 nM [1]. LDN 209929 dihydrochloride displays 180-fold selectivity on haspin kinase over DYRK2 [1]. |
GBR 13069 dihydrochloride |
B6296-10 |
ApexBio |
10 mg |
EUR 321.6 |
GBR 13069 dihydrochloride |
B6296-50 |
ApexBio |
50 mg |
EUR 1167.6 |
SKF 91488 dihydrochloride |
B6331-10 |
ApexBio |
10 mg |
EUR 265.2 |
SKF 91488 dihydrochloride |
B6331-50 |
ApexBio |
50 mg |
EUR 926.4 |
GBR 12783 dihydrochloride |
B6332-10 |
ApexBio |
10 mg |
EUR 303.6 |
GBR 12783 dihydrochloride |
B6332-50 |
ApexBio |
50 mg |
EUR 1082.4 |
BD 1063 dihydrochloride |
B6489-10 |
ApexBio |
10 mg |
EUR 205.2 |
Description: BD 1063 dihydrochloride is an antagonist of ?-1 receptor with Ki value of 9.15 nM [1].?-receptor is a type of opioid receptor. There are two subtypes of ?-receptor: ?-1 and ?-2.?-1 receptor plays an important role in stimulating dopamine release and modulating the actions of cocaine [2]. |
BD 1063 dihydrochloride |
B6489-5 |
ApexBio |
5 mg |
EUR 151.2 |
Description: BD 1063 dihydrochloride is an antagonist of ?-1 receptor with Ki value of 9.15 nM [1].?-receptor is a type of opioid receptor. There are two subtypes of ?-receptor: ?-1 and ?-2.?-1 receptor plays an important role in stimulating dopamine release and modulating the actions of cocaine [2]. |
RS 16566 dihydrochloride |
B6548-10 |
ApexBio |
10 mg |
EUR 408 |
RS 16566 dihydrochloride |
B6548-50 |
ApexBio |
50 mg |
EUR 1531.2 |
CGP 20712 dihydrochloride |
B6552-10 |
ApexBio |
10 mg |
EUR 459.6 |
Description: CGP 20712 dihydrochloride is a potent and selective antagonist of ?1-adrenoceptor with IC50 value of 0.7 nM [1]. ?1-adrenoceptor is a G-protein coupled receptor and mediates uncoupling protein-1 (UCP1) gene expression induced by norepinephrine (NE) [2]. |
CGP 20712 dihydrochloride |
B6552-50 |
ApexBio |
50 mg |
EUR 1746 |
Description: CGP 20712 dihydrochloride is a potent and selective antagonist of ?1-adrenoceptor with IC50 value of 0.7 nM [1]. ?1-adrenoceptor is a G-protein coupled receptor and mediates uncoupling protein-1 (UCP1) gene expression induced by norepinephrine (NE) [2]. |
CP 93129 dihydrochloride |
B6558-10 |
ApexBio |
10 mg |
EUR 381.6 |
CP 93129 dihydrochloride |
B6558-50 |
ApexBio |
50 mg |
EUR 1413.6 |
GR 55562 dihydrochloride |
B6572-10 |
ApexBio |
10 mg |
EUR 400.8 |
GR 55562 dihydrochloride |
B6572-50 |
ApexBio |
50 mg |
EUR 1491.6 |
RJR 2429 dihydrochloride |
B6666-10 |
ApexBio |
10 mg |
EUR 369.6 |
RJR 2429 dihydrochloride |
B6666-50 |
ApexBio |
50 mg |
EUR 1363.2 |
SCH 79797 dihydrochloride |
B6801-10 |
ApexBio |
10 mg |
EUR 285.6 |
SCH 79797 dihydrochloride |
B6801-5 |
ApexBio |
5 mg |
EUR 223.2 |
SKF 86002 dihydrochloride |
B6921-10 |
ApexBio |
10 mg |
EUR 439.2 |
SKF 86002 dihydrochloride |
B6921-50 |
ApexBio |
50 mg |
EUR 1654.8 |
GW 583340 dihydrochloride |
B6989-10 |
ApexBio |
10 mg |
EUR 439.2 |
GW 583340 dihydrochloride |
B6989-50 |
ApexBio |
50 mg |
EUR 1654.8 |
CGH 2466 dihydrochloride |
B7027-10 |
ApexBio |
10 mg |
EUR 340.8 |
Description: CGH 2466 dihydrochloride is a combined adenosine receptor antagonist. It is an inhibitor of phosphodiesterase type 4 and p38 mitogen-activated protein kinase. It inhibited the phosphodiesterase 4D (PDE4D) isoenzyme with an IC50 value of 22±5 nM. |
CGH 2466 dihydrochloride |
B7027-50 |
ApexBio |
50 mg |
EUR 1245.6 |
Description: CGH 2466 dihydrochloride is a combined adenosine receptor antagonist. It is an inhibitor of phosphodiesterase type 4 and p38 mitogen-activated protein kinase. It inhibited the phosphodiesterase 4D (PDE4D) isoenzyme with an IC50 value of 22±5 nM. |
AZ 12080282 dihydrochloride |
A8657-10 |
ApexBio |
10 mg |
EUR 498 |
Description: AZ 12080282 dihydrochloride is a selective inhibitor of Hh with IC50 value <0.012 ?M [1]. It is also reported that AZ 12080282 also has a selective inhibition to p38? with low nanomolar potency [1]. |
AZ 12080282 dihydrochloride |
A8657-50 |
ApexBio |
50 mg |
EUR 1900.8 |
Description: AZ 12080282 dihydrochloride is a selective inhibitor of Hh with IC50 value <0.012 ?M [1]. It is also reported that AZ 12080282 also has a selective inhibition to p38? with low nanomolar potency [1]. |
AY 9944 dihydrochloride |
A8658-10 |
ApexBio |
10 mg |
EUR 289.2 |
Description: AY 9944 dihydrochloride is a selective inhibitor of ?7-sterol reductase with IC50 value of 13 nM [1].?7-sterol reductase (Dhcr7) is an enzyme and plays an important role in catalyzing the production of cholesterol from 7-Dehydrocholesterol through using NADPH [2, 3]. |
AY 9944 dihydrochloride |
A8658-25 |
ApexBio |
25 mg |
EUR 582 |
Description: AY 9944 dihydrochloride is a selective inhibitor of ?7-sterol reductase with IC50 value of 13 nM [1].?7-sterol reductase (Dhcr7) is an enzyme and plays an important role in catalyzing the production of cholesterol from 7-Dehydrocholesterol through using NADPH [2, 3]. |
AY 9944 dihydrochloride |
A8658-5 |
ApexBio |
5 mg |
EUR 184.8 |
Description: AY 9944 dihydrochloride is a selective inhibitor of ?7-sterol reductase with IC50 value of 13 nM [1].?7-sterol reductase (Dhcr7) is an enzyme and plays an important role in catalyzing the production of cholesterol from 7-Dehydrocholesterol through using NADPH [2, 3]. |
CP 31398 dihydrochloride |
A4476-10 |
ApexBio |
10 mg |
EUR 381.6 |
Description: CP 31398 dihydrochloride is a potent activator of p53 with maximum tolerated dose of 400 ppm [2].Tumor protein p53 (p53) is a crucial protein in multicellular organisms and plays an important role in preventing cancer formation. |
CP 31398 dihydrochloride |
A4476-50 |
ApexBio |
50 mg |
EUR 1413.6 |
Description: CP 31398 dihydrochloride is a potent activator of p53 with maximum tolerated dose of 400 ppm [2].Tumor protein p53 (p53) is a crucial protein in multicellular organisms and plays an important role in preventing cancer formation. |
RN 1 dihydrochloride |
B2080-25 |
Biovision |
each |
EUR 705.6 |
RN 1 dihydrochloride |
B2080-5 |
Biovision |
each |
EUR 222 |
H-9 dihydrochloride |
B5001-25 |
ApexBio |
25 mg |
EUR 217.2 |
H-9 dihydrochloride |
B5001-50 |
ApexBio |
50 mg |
EUR 339.6 |
RN 1 dihydrochloride |
B5784-10 |
ApexBio |
10 mg |
EUR 447.6 |
Description: RN 1 dihydrochloride is a potent and selective inhibitor of LSD1 with IC50 value of 70 nM [1]. |
RN 1 dihydrochloride |
B5784-50 |
ApexBio |
50 mg |
EUR 1695.6 |
Description: RN 1 dihydrochloride is a potent and selective inhibitor of LSD1 with IC50 value of 70 nM [1]. |
PB 28 dihydrochloride |
B7107-10 |
ApexBio |
10 mg |
EUR 340.8 |
PB 28 dihydrochloride |
B7107-50 |
ApexBio |
50 mg |
EUR 1245.6 |
H-7 dihydrochloride |
B6342-10 |
ApexBio |
10 mg |
EUR 188.4 |
H-7 dihydrochloride |
B6342-25 |
ApexBio |
25 mg |
EUR 360 |
H-7 dihydrochloride |
B6342-5 |
ApexBio |
5 mg |
EUR 134.4 |
H-7 dihydrochloride |
B6342-50 |
ApexBio |
50 mg |
EUR 584.4 |
MM 77 dihydrochloride |
B6511-10 |
ApexBio |
10 mg |
EUR 340.8 |
MM 77 dihydrochloride |
B6511-50 |
ApexBio |
50 mg |
EUR 1245.6 |
H-7 dihydrochloride |
9543-25 |
Biovision |
each |
EUR 652.8 |
H-7 dihydrochloride |
9543-5 |
Biovision |
each |
EUR 210 |
ABT 702 dihydrochloride |
B5298-10 |
ApexBio |
10 mg |
EUR 494.4 |
Description: IC50: 1.7 nM for adenosine kinaseAdenosine (ADO) is an endogenous homeostatic inhibitory neuromodulator that reduces cellular excitability at sites of tissue injury and inflammation. |
ABT 702 dihydrochloride |
B5298-100 |
ApexBio |
100 mg |
EUR 2049.6 |
Description: IC50: 1.7 nM for adenosine kinaseAdenosine (ADO) is an endogenous homeostatic inhibitory neuromodulator that reduces cellular excitability at sites of tissue injury and inflammation. |
ABT 702 dihydrochloride |
B5298-5 |
ApexBio |
5 mg |
EUR 331.2 |
Description: IC50: 1.7 nM for adenosine kinaseAdenosine (ADO) is an endogenous homeostatic inhibitory neuromodulator that reduces cellular excitability at sites of tissue injury and inflammation. |
ABT 702 dihydrochloride |
B5298-5.1 |
ApexBio |
10 mM (in 1mL DMSO) |
EUR 379.2 |
Description: IC50: 1.7 nM for adenosine kinaseAdenosine (ADO) is an endogenous homeostatic inhibitory neuromodulator that reduces cellular excitability at sites of tissue injury and inflammation. |
ABT 702 dihydrochloride |
B5298-50 |
ApexBio |
50 mg |
EUR 1417.2 |
Description: IC50: 1.7 nM for adenosine kinaseAdenosine (ADO) is an endogenous homeostatic inhibitory neuromodulator that reduces cellular excitability at sites of tissue injury and inflammation. |
C 021 dihydrochloride |
B5457-1 |
ApexBio |
1 mg |
EUR 135.6 |
Description: C 021 dihydrochloride is a potent antagonist of CCR4 with IC50 values of 0.039 and 0.14 ?M for inhibition of chemotaxis in mouse and human, respectively [1]. |
C 021 dihydrochloride |
B5457-5 |
ApexBio |
5 mg |
EUR 309.6 |
Description: C 021 dihydrochloride is a potent antagonist of CCR4 with IC50 values of 0.039 and 0.14 ?M for inhibition of chemotaxis in mouse and human, respectively [1]. |
TCN 237 dihydrochloride |
B5523-10 |
ApexBio |
10 mg |
EUR 320.4 |
TCN 237 dihydrochloride |
B5523-5 |
ApexBio |
5 mg |
EUR 254.4 |
VU 590 dihydrochloride |
B7526-10 |
ApexBio |
10 mg |
EUR 284.4 |
VU 590 dihydrochloride |
B7526-50 |
ApexBio |
50 mg |
EUR 1004.4 |
ML 786 dihydrochloride |
B7736-10 |
ApexBio |
10 mg |
EUR 583.2 |
Description: IC50: 2.1, 2.5 and 4.2 nM for B-RafV600E, C-Raf and wild-type B-Raf, respectivelyML 786 is a potent Raf kinase inhibitor. |
ARC 239 dihydrochloride |
B6508-25 |
ApexBio |
25 mg |
EUR 642 |
Description: ARC 239 dihydrochloride is a selective antagonist of ?2B adrenoceptor with pKD value of 8.8 [1]. ?2B adrenoceptor is a G-protein coupled receptor. |
ARC 239 dihydrochloride |
B6508-5 |
ApexBio |
5 mg |
EUR 212.4 |
Description: ARC 239 dihydrochloride is a selective antagonist of ?2B adrenoceptor with pKD value of 8.8 [1]. ?2B adrenoceptor is a G-protein coupled receptor. |
XE 991 dihydrochloride |
B6917-10 |
ApexBio |
10 mg |
EUR 214.8 |
XE 991 dihydrochloride |
B6917-5 |
ApexBio |
5 mg |
EUR 141.6 |
XE 991 dihydrochloride |
B6917-50 |
ApexBio |
50 mg |
EUR 714 |
AMN 082 dihydrochloride |
B7034-10 |
ApexBio |
10 mg |
EUR 284.4 |
Description: AMN 082 dihydrochloride is an specific allosteric agonist of mGluR7 [1]. In the absence of orthosteric agonist, AMN 082 activated the human mGlu7 receptor with an EC50 of 64 nM in vitro [2]. |
AMN 082 dihydrochloride |
B7034-50 |
ApexBio |
50 mg |
EUR 1004.4 |
Description: AMN 082 dihydrochloride is an specific allosteric agonist of mGluR7 [1]. In the absence of orthosteric agonist, AMN 082 activated the human mGlu7 receptor with an EC50 of 64 nM in vitro [2]. |
SA4503 dihydrochloride |
B3046-25 |
Biovision |
25 mg |
EUR 612 |
SA4503 dihydrochloride |
B3046-5 |
Biovision |
5 mg |
EUR 199.2 |
AT7867 dihydrochloride |
A3199-10 |
ApexBio |
10 mg |
EUR 408 |
Description: IC50: AKT1 32 nM, AKT2 17 nM, AKT3 47 nM, PKA 20 nMThe serine/threonine kinase AKT plays a pivotal role in signal transduction events involved in malignant transformation and chemoresistance and is an attractive target for the development of cancer therapeutics. |
AT7867 dihydrochloride |
A3199-100 |
ApexBio |
100 mg |
EUR 2210.4 |
Description: IC50: AKT1 32 nM, AKT2 17 nM, AKT3 47 nM, PKA 20 nMThe serine/threonine kinase AKT plays a pivotal role in signal transduction events involved in malignant transformation and chemoresistance and is an attractive target for the development of cancer therapeutics. |
AT7867 dihydrochloride |
A3199-5 |
ApexBio |
5 mg |
EUR 320.4 |
Description: IC50: AKT1 32 nM, AKT2 17 nM, AKT3 47 nM, PKA 20 nMThe serine/threonine kinase AKT plays a pivotal role in signal transduction events involved in malignant transformation and chemoresistance and is an attractive target for the development of cancer therapeutics. |
AT7867 dihydrochloride |
A3199-5.1 |
ApexBio |
10 mM (in 1mL DMSO) |
EUR 344.4 |
Description: IC50: AKT1 32 nM, AKT2 17 nM, AKT3 47 nM, PKA 20 nMThe serine/threonine kinase AKT plays a pivotal role in signal transduction events involved in malignant transformation and chemoresistance and is an attractive target for the development of cancer therapeutics. |
AT7867 dihydrochloride |
A3199-50 |
ApexBio |
50 mg |
EUR 1537.2 |
Description: IC50: AKT1 32 nM, AKT2 17 nM, AKT3 47 nM, PKA 20 nMThe serine/threonine kinase AKT plays a pivotal role in signal transduction events involved in malignant transformation and chemoresistance and is an attractive target for the development of cancer therapeutics. |
LDK378 dihydrochloride |
A3544-10 |
ApexBio |
10 mg |
EUR 186 |
Description: LDK378 is a highly potent inhibitor of anaplastic lymphoma kinase (ALK), which is a receptor tyrosine kinase belonging to the superfamily of insulin receptor, with half maximal inhibitory concentration IC50 of 200 pM. |
LDK378 dihydrochloride |
A3544-100 |
ApexBio |
100 mg |
EUR 331.2 |
Description: LDK378 is a highly potent inhibitor of anaplastic lymphoma kinase (ALK), which is a receptor tyrosine kinase belonging to the superfamily of insulin receptor, with half maximal inhibitory concentration IC50 of 200 pM. |
PPACK Dihydrochloride