IMPORTANCE OF ZINC CONCENTRATION IN SEMINAL FLUID OF MEN DIAGNOSED WITH INFERTILITY

The prevalence and importance of male infertility makes medical and social problems that seriously throughout the world. The purpose of this study was to determine whether there is a significant difference in the concentration of zinc in seminal fluid in men diagnosed with infertility compared with the control group, and if there is, to determine how it affects the number and percentage of sperm motility were normal and morphology.

A case-control study conducted in Osijek-Baranja County from January 2014 to June 2015. The study included 276 subjects called biochemical laboratory of Osijek University Central Hospital, 100 (36.2%) of those with a low sperm count was confirmed by spermiogram after 3 months. the semen sample is processed in accordance with the criteria of the World Health Organization, and the zinc concentration was determined by spectrophotometry and colorimetric directly without deproteinization on chemical analysis (Olympus AU 680, Beckman Coulter, Tokyo, Japan).

The study shows that men with low sperm counts were significantly older (Mann Whitney U test: p = 0.013) and had lower levels of zinc (χ2-test: p <0.001). Further analysis included 100 (36.2%) patients with low sperm count. In the group of infertile men, men with low sperm counts have higher levels of zinc compared with men with azoospermia (Mann Whitney U test: p = 0.036), indicating a relationship between low zinc levels in the fertility of male fluid and semen.

Zinc as biological markers and antioxidants affect the sperm count, motility and morphology. Therapeutic zinc supplements may improve semen parameters in patients diagnosed with a low sperm count. dietary habits of different regional subjects, and future research can create a solid foundation for complementary approach to the treatment of male infertility.

 IMPORTANCE OF ZINC CONCENTRATION IN SEMINAL FLUID OF MEN DIAGNOSED WITH INFERTILITY
IMPORTANCE OF ZINC CONCENTRATION IN SEMINAL FLUID OF MEN DIAGNOSED WITH INFERTILITY

Effect of broiler genetics, age, and gender on performance and blood chemistry

A total of 640 broilers were used to determine the effects of strain, sex, and age on hematology and blood chemistry using a rapid detection. Day old chicks from two genetic lines of the common broiler strains of fast-growing and high yield sexed and allocated to 40 pens (16 birds per pen) containing either male or female and Ross or Cobb strains (n ​​= 10). Venous blood was analyzed weekly using 2 broilers from each pen (n = 20) using the Clinical Analyzer i-STAT® Alinity Handheld, Zoetis Vetscan VS2, and the device iCheck ™ Carotene at 14, 21, 28, 35, and 42 d, as as well as growth performance. Post-mortem health tracking metrics is also recorded on 42 d. Broiler considered healthy based on data posts and conducted in accordance with industry standards by males presenting a larger BW and reduced FCR of broilers women.

Ross broiler larger display BW for 14 d with the same FCR compared to Cobb birds. Days of age had a very significant impact on blood calcium, phosphorus, potassium, sodium, chloride, carotene, aspartate aminotransferase, creatine kinase, bile acid, uric acid, total protein, albumin, globulin, total carbon dioxide, hematocrit, and malondialdehyde. male broilers had reduced blood sodium, chloride, carotene, uric acid, albumin, and increased total protein, glucose, and total carbon dioxide.

Histamine dihydrochloride

GE0339-5 5
EUR 45.1

H89 Dihydrochloride

20-abx076747
  • EUR 811.20
  • EUR 360.00
  • 25 mg
  • 5 mg

MPP dihydrochloride

B6910-10 10 mg
EUR 381.6

MPP dihydrochloride

B6910-50 50 mg
EUR 1413.6

SAG dihydrochloride

GL1175-1MG 1 mg
EUR 234

SAG dihydrochloride

GL1175-5MG 5 mg
EUR 688.8

TMB (dihydrochloride)

HY-15930A 10mM/1mL
EUR 135.6

TMB dihydrochloride

TB0514 1g
EUR 85.06

SAG dihydrochloride

GL1175-1 1
EUR 98.4

SAG dihydrochloride

GL1175-25 25
EUR 334.3

SAG dihydrochloride

GL1175-5 5
EUR 169

1400W dihydrochloride

2055-25 each
EUR 405.6

1400W dihydrochloride

2055-5 each
EUR 151.2

DMPQ Dihydrochloride

20-abx076714
  • EUR 693.60
  • EUR 326.40
  • 25 mg
  • 5 mg

IT1t dihydrochloride

B5650-10 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

B5650-100 100 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 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 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 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 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.

DMPQ dihydrochloride

B6642-10 10 mg
EUR 223.2

DMPQ dihydrochloride

B6642-5 5 mg
EUR 184.8

GNTI dihydrochloride

B6669-10 10 mg
EUR 459.6

GNTI dihydrochloride

B6669-50 50 mg
EUR 1746

1400W dihydrochloride

B6730-10 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

B6730-100 100 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 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.

1400W dihydrochloride

GK6799-100MG 100 mg
EUR 661.2

1400W dihydrochloride

GK6799-25MG 25 mg
EUR 274.8

1400W dihydrochloride

GK6799-5MG 5 mg
EUR 136.8

PAβN (dihydrochloride)

HY-101444A 10mM/1mL
EUR 154.8

IT1t (dihydrochloride)

HY-101458A 10mg
EUR 308.4

1400W (Dihydrochloride)

HY-18731 10mM/1mL
EUR 151.2

DAPI (dihydrochloride)

HY-D0814 50mg
EUR 439.2

1400W dihydrochloride

GK6799-100 100
EUR 605.5

1400W dihydrochloride

GK6799-25 25
EUR 228.1

1400W dihydrochloride

GK6799-5 5
EUR 86.5

GGACK Dihydrochloride

1847-5 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.

PPACK Dihydrochloride

1848-5 each
EUR 301.2

GGACK Dihydrochloride

A2582-5 5 mg
EUR 282
Description: A potent and irreversible inhibitor of Urokinase (uPA (IC??<1 µM), Factor VIIa, Factor IXa, Factor Xa, and trypsin.

PPACK Dihydrochloride

A2588-10 10 mg
EUR 423.6
Description: PPACK Dihydrochloride is the dihydrochloride form of its active component PPACK (D-Phenylalanyl-L-prolyl-L-arginine chloromethyl ketone), a potent, selective and irreversible inhibitor of thrombin that inhibits human ?-thrombin with inhibition constant Kivalue of 0.24 nM.

PPACK Dihydrochloride

A2588-25 25 mg
EUR 908.4
Description: PPACK Dihydrochloride is the dihydrochloride form of its active component PPACK (D-Phenylalanyl-L-prolyl-L-arginine chloromethyl ketone), a potent, selective and irreversible inhibitor of thrombin that inhibits human ?-thrombin with inhibition constant Kivalue of 0.24 nM.

PPACK Dihydrochloride

A2588-5 5 mg
EUR 265.2
Description: PPACK Dihydrochloride is the dihydrochloride form of its active component PPACK (D-Phenylalanyl-L-prolyl-L-arginine chloromethyl ketone), a potent, selective and irreversible inhibitor of thrombin that inhibits human ?-thrombin with inhibition constant Kivalue of 0.24 nM.

JDTic (dihydrochloride)

HY-10487 50mg
EUR 1501.2

MS023 (dihydrochloride)

HY-19615B 100mg
EUR 1093.2

DG172 (dihydrochloride)

HY-19737A 50mg
EUR 704.4

CP 31398 dihydrochloride

A4476-10 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 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.

AZ 12080282 dihydrochloride

A8657-10 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 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 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 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 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].

GBR 12935 dihydrochloride

B4661-10 10 mg
EUR 129.6

GBR 12935 dihydrochloride

B4661-100 100 mg
EUR 296.4

GBR 12935 dihydrochloride

B4661-50 50 mg
EUR 192

ETP 45835 dihydrochloride

B4938-10 10 mg
EUR 428.4

ETP 45835 dihydrochloride

B4938-50 50 mg
EUR 1608

AZ 10606120 dihydrochloride

B5410-10 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 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 10 mg
EUR 478.8

CP 99994 dihydrochloride

B5422-50 50 mg
EUR 1824

SB 243213 dihydrochloride

B5444-10 10 mg
EUR 486

SB 243213 dihydrochloride

B5444-50 50 mg
EUR 1802.4

JNJ 5207852 dihydrochloride

B5513-10 10 mg
EUR 289.2

JNJ 5207852 dihydrochloride

B5513-5 5 mg
EUR 180

JNJ 5207852 dihydrochloride

B5513-50 50 mg
EUR 1021.2

A 412997 dihydrochloride

B5639-25 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 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 10 mg
EUR 297.6

SA 4503 dihydrochloride

B5778-5.1 10 mM (in 1mL DMSO)
EUR 343.2

SA 4503 dihydrochloride

B5778-50 50 mg
EUR 1069.2

BMS 599626 dihydrochloride

B5792-10 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].

GBR 13069 dihydrochloride

B6296-10 10 mg
EUR 321.6

GBR 13069 dihydrochloride

B6296-50 50 mg
EUR 1167.6

SKF 91488 dihydrochloride

B6331-10 10 mg
EUR 265.2

SKF 91488 dihydrochloride

B6331-50 50 mg
EUR 926.4

GBR 12783 dihydrochloride

B6332-10 10 mg
EUR 303.6

GBR 12783 dihydrochloride

B6332-50 50 mg
EUR 1082.4

BD 1063 dihydrochloride

B6489-10 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 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 10 mg
EUR 408

RS 16566 dihydrochloride

B6548-50 50 mg
EUR 1531.2

CGP 20712 dihydrochloride

B6552-10 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 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 10 mg
EUR 381.6

CP 93129 dihydrochloride

B6558-50 50 mg
EUR 1413.6

GR 55562 dihydrochloride

B6572-10 10 mg
EUR 400.8

GR 55562 dihydrochloride

B6572-50 50 mg
EUR 1491.6

TC 1698 dihydrochloride

B7089-10 10 mg
EUR 408

TC 1698 dihydrochloride

B7089-50 50 mg
EUR 1531.2

JP 1302 dihydrochloride

B7147-10 10 mg
EUR 466.8

JP 1302 dihydrochloride

B7147-50 50 mg
EUR 1771.2

BYK 191023 dihydrochloride

B7210-10 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 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 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 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 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 10 mg
EUR 369.6

PD 168568 dihydrochloride

B7420-50 50 mg
EUR 1363.2

A 943931 dihydrochloride

B7495-10 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 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 10 mg
EUR 309.6

PG 01037 dihydrochloride

B7524-25 25 mg
EUR 633.6

PG 01037 dihydrochloride

B7524-5 5 mg
EUR 195.6

WAY 207024 dihydrochloride

B7525-10 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 10 mg
EUR 289.2

WAY 208466 dihydrochloride

B7531-25 25 mg
EUR 582

WAY 208466 dihydrochloride

B7531-5 5 mg
EUR 184.8

WAY 267464 dihydrochloride

B7538-10 10 mg
EUR 556.8

JNJ 10181457 dihydrochloride

B7567-10 10 mg
EUR 466.8

JNJ 10181457 dihydrochloride

B7567-50 50 mg
EUR 1771.2

BMS 470539 dihydrochloride

B7577-10 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 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 25 mg
EUR 428.4

PS 1145 dihydrochloride

B7683-5 5 mg
EUR 164.4

A 331440 dihydrochloride

B7698-10 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 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 10 mg
EUR 466.8

R 1485 dihydrochloride

B7723-50 50 mg
EUR 1771.2

DBM 1285 dihydrochloride

B7748-10 10 mg
EUR 517.2

DBM 1285 dihydrochloride

B7748-50 50 mg
EUR 1987.2

LDN 209929 dihydrochloride

B7785-10 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 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].

RJR 2429 dihydrochloride

B6666-10 10 mg
EUR 369.6

RJR 2429 dihydrochloride

B6666-50 50 mg
EUR 1363.2

SCH 79797 dihydrochloride

B6801-10 10 mg
EUR 285.6

SCH 79797 dihydrochloride

B6801-5 5 mg
EUR 223.2

SKF 86002 dihydrochloride

B6921-10 10 mg
EUR 439.2

SKF 86002 dihydrochloride

B6921-50 50 mg
EUR 1654.8

GW 583340 dihydrochloride

B6989-10 10 mg
EUR 439.2

GW 583340 dihydrochloride

B6989-50 50 mg
EUR 1654.8

CGH 2466 dihydrochloride

B7027-10 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 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.

GBR 12935 (dihydrochloride)

HY-12242 10mg
EUR 142.8

GBR 12783 (dihydrochloride)

HY-100968 5mg
EUR 267.6

H-7 dihydrochloride

9543-25 each
EUR 652.8

H-7 dihydrochloride

9543-5 each
EUR 210

RN 1 dihydrochloride

B2080-25 each
EUR 705.6

RN 1 dihydrochloride

B2080-5 each
EUR 222

H-9 dihydrochloride

B5001-25 25 mg
EUR 217.2

H-9 dihydrochloride

B5001-50 50 mg
EUR 339.6

RN 1 dihydrochloride

B5784-10 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 50 mg
EUR 1695.6
Description: RN 1 dihydrochloride is a potent and selective inhibitor of LSD1 with IC50 value of 70 nM [1].

H-7 dihydrochloride

B6342-10 10 mg
EUR 188.4

H-7 dihydrochloride

B6342-25 25 mg
EUR 360

H-7 dihydrochloride

B6342-5 5 mg
EUR 134.4

H-7 dihydrochloride

B6342-50 50 mg
EUR 584.4

MM 77 dihydrochloride

B6511-10 10 mg
EUR 340.8

MM 77 dihydrochloride

B6511-50 50 mg
EUR 1245.6

PB 28 dihydrochloride

B7107-10 10 mg
EUR 340.8

PB 28 dihydrochloride

B7107-50 50 mg
EUR 1245.6

H-8 dihydrochloride

GK6037-10MG 10 mg
EUR 136.8

H-8 dihydrochloride

GK6037-50MG 50 mg
EUR 302.4

H-8 dihydrochloride

GK6037-10 10
EUR 86.5

H-8 dihydrochloride

GK6037-50 50
EUR 210.3

ABT 702 dihydrochloride

B5298-10 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

B5298-100 100 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 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 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 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 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 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 10 mg
EUR 320.4

TCN 237 dihydrochloride

B5523-5 5 mg
EUR 254.4

ARC 239 dihydrochloride

B6508-25 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 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.

VU 590 dihydrochloride

B7526-10 10 mg
EUR 284.4

VU 590 dihydrochloride

B7526-50 50 mg
EUR 1004.4

ML 786 dihydrochloride

B7736-10 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.

XE 991 dihydrochloride

B6917-10 10 mg
EUR 214.8

XE 991 dihydrochloride

B6917-5 5 mg
EUR 141.6

XE 991 dihydrochloride

B6917-50 50 mg
EUR 714

AMN 082 dihydrochloride

B7034-10 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 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].

AT7867 dihydrochloride

A3199-10 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

A3199-100 100 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 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 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 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 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

A3544-100 100 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.

LDK378 dihydrochloride

A3544-5 5 mg
EUR 150
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

A3544-5.1 10 mM (in 1mL H2O)
EUR 184.8
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

A3544-50 50 mg
EUR 240
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.

SA4503 dihydrochloride

B3046-25 25 mg
EUR 612

SA4503 dihydrochloride

B3046-5 5 mg
EUR 199.2

AT7867 (dihydrochloride)

HY-12059A 100mg
EUR 1695.6

JPH203 Dihydrochloride

HY-U00445 100mg
EUR 1135.2

LCL521 dihydrochloride

HY-103593A 10mg
EUR 817.2

Ross broilers had greater blood potassium, and sodium, as well as reduce uric acid, total protein, globulin, and malondialdehyde, compared to Cobb birds. These results demonstrate the effectiveness of point-of-care device for measuring blood chemistry and hematology in the modern broiler. This data can be used to determine normal ranges of healthy blood in this kind of broiler when accounting for the strain, sex, and age.