Growth and structural studies of In/Au(111) alloys and InOx/Au(111) inverse oxide/metal model catalysts.

Indium oxide has received attention as an attractive candidate to catalyze the hydrogenation of CO2 to methanol as a high selectivity (> 80%). Compared with the level of research activity indium oxide-based catalyst powder, very little is known about the phenomena associated with the formation of surface alloys involves indium or indium oxide nanoparticle growth mechanisms.

In this report, scanning tunneling microscopy and X-ray photoelectron spectroscopy (XPS) was employed to explain the mode of growth, structure, and chemical states in / Au (111) and Inox alloy / Au (111) inverse model catalysts. Our study shows that different morphological differences between the In / Au (111) and Inox / Au (111), and the structure of Inox also very dependent on the preparation conditions. In / Au system alloy surface with very low coverage (0.02 ML) in the form of islands of privilege on the elbow sites reconstructed Au (111) herringbone, regardless of closed packed hexagonal and face-centered cubic stacking.

At higher coverage (0.1 ML), in the island extending over herringbone towards ⟨110⟩ and creating two-dimensional domain structure over the entire surface. In addition, the 2D domain structure is disrupted by temperature with high dispersion of indium atoms were observed during the annealing process. Oxidation of In / Au (111) surface alloys with O2 at 550 K produces Inox / Au (111) system containing various sizes of aggregate Inox (from 0.7 nm to 10 nm). On the other hand, Inox / Au (111) surface was prepared by vapor deposition of In at 550 K in the background of the exhibition O2 highly dispersed and uniform Inox small particles (~ 1 nm). Both systems Inox confirmed to partially oxidized by XPS.

Tris-HCl, 1M, 1XpH 7.4
USD8125 500ml
EUR 93.41

1M Tris-HCl Buffer, pH 7.4
T9301-050 500ml
EUR 144

1M Tris-HCl Buffer, pH 8.0
T9302-050 500ml
EUR 144

1M Tris-HCl Buffer, pH 8.5
T9303-050 500ml
EUR 144

Tris-HCl, 1M, 1X, pH 8.0
USD8127 500ml
EUR 93.41

Tris-HCl, 1M, 1X, pH 7.0
USD8137 500ml
EUR 93.41

1L Tris-HCL 1M pH 7.2
NAT1290 1L
EUR 75.24

1L Tris-HCL 1M pH 7.4
NAT1292 1L
EUR 75.24

1L Tris-HCL 1M pH 7.6
NAT1294 1L
EUR 75.24

Tris EDTA Saline, 10mM Tris HCl , 1mM EDTA, 2M Nacl
T8059-010 100ml
EUR 91.2

Tris EDTA Saline, 10mM Tris HCl , 1mM EDTA, 2M Nacl
T8059-050 500ml
EUR 100.8

Tris EDTA Saline, 10mM Tris HCl , 1mM EDTA, 2M Nacl
T8059-101 1L
EUR 151.2

Tris EDTA Saline, 10mM Tris HCl , 1mM EDTA, 2M Nacl
T8150-050 500 ml
EUR 100.8

Tris EDTA Saline, 10mM Tris HCl , 1mM EDTA, 2M Nacl
T8150-801 8L
EUR 144

TCEP*HCl;TRIS(2-CARBOXYETHYL)PHOSPHINE HYDROCHLORIDE
20-abx184392
  • EUR 811.20
  • EUR 410.40
  • EUR 243.60
  • 100 g
  • 25 g
  • 5 g

10xTM buffer (Tris-HCl, Magnesium Sulfate), sterile
SD8107 1L
EUR 91.32

Tris HCl Buffer 0.5M Solution, Sterile pH 6.8
SD8122 450ml
EUR 93.41

Tris HCl Buffer 1M Solution, Sterile pH 7.5
SD8124 450ml
EUR 93.41

Tris HCl Buffer 1M Solution, Sterile pH 8.0
SD8127 450ml
EUR 93.41

Tris HCl Buffer 1M Solution, Sterile pH 10.0
SD8129 450ml
EUR 93.41

Tris HCl Buffer 1M Solution, Sterile pH 7.0
SD8137 450ml
EUR 93.41

Tris HCl Buffer 1M Solution, Sterile pH 8.5
SD8141 450ml
EUR 93.41

Tris HCl Buffer 1M Solution, Sterile pH 9.0
SD8146 450ml
EUR 93.41

TRIS
CH058 500 g
EUR 165.6

TRIS
CH059 1kg (2 x 500g [CH058])
EUR 188.4

TRIS
CH060 5kg (10 x 500g [CH058])
EUR 454.8

Tris
16-0021-500 500 g
EUR 102

TRIS
GP7166-100G 100 g
EUR 52.8

TRIS
GP7166-1KG 1 kg
EUR 97.2

TRIS
GP7166-250G 250 g
EUR 62.4

TRIS
GP7166-500G 500 g
EUR 72

Tris
TB0197 500g
EUR 103.5

Tris-Phenolis
abx082108-250ml 250 ml
EUR 226.8

Tris-base
20-abx082498
  • EUR 393.60
  • EUR 243.60
  • EUR 493.20
  • 1 kg
  • 500 g
  • 5 kg

Bis-Tris
BB0079 25g
EUR 74.62

TRIS hydrochloride
B7299-500000 500 g
EUR 309.6

Tris DBA
B7402-50 50 mg
EUR 174

BIS-TRIS
B7772-100000 100 g
EUR 321.6

TRIS hydrochloride
GB4431-100G 100 g
EUR 64.8

TRIS hydrochloride
GB4431-1KG 1 kg
EUR 160.8

TRIS hydrochloride
GB4431-250G 250 g
EUR 76.8

TRIS hydrochloride
GB4431-500G 500 g
EUR 103.2

TRIS hydrochloride
GB4431-5KG 5 kg
EUR 486

BIS-TRIS
GB6605-100G 100 g
EUR 93.6

BIS-TRIS
GB6605-1KG 1 kg
EUR 409.2

BIS-TRIS
GB6605-250G 250 g
EUR 151.2

BIS-TRIS
GB6605-25G 25 g
EUR 60

BIS-TRIS
GB6605-500G 500 g
EUR 246

TRIS acetate
GB8936-500G 500 g
EUR 342

Fostemsavir Tris
HY-15440B 5mg
EUR 308.4

Tris hydrochloride
TB0103 250g
EUR 84.01

Tris acetate
TD0101 100g
EUR 103.15

250G Tris
NAT1050 250G
EUR 48.79

TRIS Electrode
924030 EACH
EUR 192.66

TRIS 500G
17132101 EACH
EUR 80.94

Rat Monoclonal Anti-Dinitrophenyl (DNP) IgG1, aff pure (w/o azide)
DNP15-MW 100 ug
EUR 534

Magnetic Wand with rubber grips for SPINE caps
MW-1C 1 WAND
EUR 155
Description: Magnetic Wand with rubber grips for SPINE caps

Bis-Tris Propane
BB0238 50g
EUR 128.9

BIS-TRIS hydrochloride
GK3758-100G 100 g
EUR 217.2

BIS-TRIS hydrochloride
GK3758-250G 250 g
EUR 380.4

BIS-TRIS hydrochloride
GK3758-25G 25 g
EUR 98.4

BIS-TRIS propane
GB2945-100G 100 g
EUR 180

BIS-TRIS propane
GB2945-250G 250 g
EUR 322.8

BIS-TRIS propane
GB2945-25G 25 g
EUR 84

BIS-TRIS propane
GB2945-500G 500 g
EUR 562.8

Ketorolac tris salt
GP8482-100MG 100 mg
EUR 90

Bis-Tris, 250g
R6976-250g
EUR 228

Bis-Tris, 500g
R6976-500g
EUR 370.8

Tris - Biotech Grade
TB0196 500g
EUR 86.1

Tris-(hydroxymethyl) propane
T1491 100g
EUR 90.28

1KG Tris Ultrapure
NAT1052 1KG
EUR 133.38

Tris (Molecular Biology Grade)
CE237 500 g
EUR 106.8

Tris (Molecular Biology Grade)
CE238 1 kg
EUR 153.6

Tris (Molecular Biology Grade)
CE239 5 kg
EUR 535.2

CEA protein (in TRIS)
30-AC26 1 mg
EUR 496.8
Description: Purified native Human CEA protein

Bis-tris (hydroxymethyl) aminomethane
abx082231-5g 5 g
EUR 210

Tris(2,2,2-trifluoroethyl) Borate
20-abx182700
  • EUR 627.60
  • EUR 276.00
  • 10 g
  • 1 g

Tris(dibenzylideneacetone)dipalladium(0)
20-abx184467
  • EUR 1796.40
  • EUR 594.00
  • EUR 276.00
  • 100 g
  • 25 g
  • 5 g

1,1,1-Tris(hydroxymethyl)ethane
20-abx186111
  • EUR 226.80
  • EUR 260.40
  • 100 g
  • 500 g

tris(2,2,2-trifluoroethyl) borate
B8211-10 10 mg
EUR 129.6

tris(2,2,2-trifluoroethyl) borate
B8211-50 50 mg
EUR 226.8

1.5M Tris-HCI,pH8.8
AR1162 100mL
EUR 72

1M Tris-HCI,pH6.8
AR1163 100mL
EUR 72

Tris(4-aminophenyl)methane
HY-D0306 500mg
EUR 224.4

SDS-Urea-Tris solution
SB8896 500ml
EUR 89.23

Tris - Ultra Pure Grade
TB0194 500g
EUR 89.23

0.5M Tris Buffer (pH6.8)
T8102-010 100ml
EUR 96

0.5M Tris Buffer (pH6.8)
T8102-050 500ml
EUR 105.6

0.5M Tris Buffer (pH6.8)
T8102-100 2x500ml
EUR 121.2

Tris Base, Ultra Pure
T9200-100 1kg
EUR 200.4

Tris Base , Ultra Pure
T9200-500 5kg
EUR 619.2

Tris(23-dibromopropyl)phosphate
S-3773 1ML
EUR 69.54

HALO glass electrode TRIS
PHE1026 EACH
EUR 281.58

HCl Dilution Matrix (10g/l HCl)
HADM1 1L
EUR 107.16

HCl Dilution Matrix 10g/L HCl
HADM1A 2ML
EUR 98.04

Arbidol HCl
A8362-10 10 mg
EUR 129.6
Description: Arbidol (Umifenovir) hydrochloride is an broad-spectrum antiviral chemical agent which can inhibit cell entry of enveloped viruses by blocking viral fusion with host cell membrane.

Arbidol HCl
A8362-100 100 mg
EUR 421.2
Description: Arbidol (Umifenovir) hydrochloride is an broad-spectrum antiviral chemical agent which can inhibit cell entry of enveloped viruses by blocking viral fusion with host cell membrane.

Arbidol HCl
A8362-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: Arbidol (Umifenovir) hydrochloride is an broad-spectrum antiviral chemical agent which can inhibit cell entry of enveloped viruses by blocking viral fusion with host cell membrane.

Conivaptan HCl
A8402-10 10 mg
EUR 166.8
Description: Conivaptan Hydrochloride is a non-peptide inhibitor of antidiuretic hormone. Conivaptan Hydrochloride is used for treatment of congestive heart failure.

Conivaptan HCl
A8402-100 100 mg
EUR 808.8
Description: Conivaptan Hydrochloride is a non-peptide inhibitor of antidiuretic hormone. Conivaptan Hydrochloride is used for treatment of congestive heart failure.

Conivaptan HCl
A8402-5.1 10 mM (in 1mL DMSO)
EUR 181.2
Description: Conivaptan Hydrochloride is a non-peptide inhibitor of antidiuretic hormone. Conivaptan Hydrochloride is used for treatment of congestive heart failure.

Dicyclomine HCl
A8409-1000 1 g
EUR 517.2
Description: Used as a gastrointestinal antispasmodic antacid.

Dicyclomine HCl
A8409-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Used as a gastrointestinal antispasmodic antacid.

Dicyclomine HCl
A8409-5000 5 g
EUR 1198.8
Description: Used as a gastrointestinal antispasmodic antacid.

Difloxacin HCl
A8411-1000 1 g
EUR 142.8
Description: Difloxacin HCl is a quinolone antimicrobial antibiotic [1]. Quinolone antibiotics target bacterial DNA gyrase which is required during DNA replication, subsequent DNA synthesis and ultimately cell division.

Difloxacin HCl
A8411-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Difloxacin HCl is a quinolone antimicrobial antibiotic [1]. Quinolone antibiotics target bacterial DNA gyrase which is required during DNA replication, subsequent DNA synthesis and ultimately cell division.

Difloxacin HCl
A8411-5000 5 g
EUR 301.2
Description: Difloxacin HCl is a quinolone antimicrobial antibiotic [1]. Quinolone antibiotics target bacterial DNA gyrase which is required during DNA replication, subsequent DNA synthesis and ultimately cell division.

Diperodon HCl
A8413-100 100 mg
EUR 129.6
Description: Diperodon HCl

Diperodon HCl
A8413-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Diperodon HCl

Diphenylpyraline HCl
A8415-1000 1 g
EUR 517.2
Description: Diphenylpyraline is a first-generation antihistamine with anticholinergic effects of the diphenylpiperidine class.

Diphenylpyraline HCl
A8415-10000 10 g
EUR 1783.2
Description: Diphenylpyraline is a first-generation antihistamine with anticholinergic effects of the diphenylpiperidine class.

Diphenylpyraline HCl
A8415-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Diphenylpyraline is a first-generation antihistamine with anticholinergic effects of the diphenylpiperidine class.

Diphenylpyraline HCl
A8415-5000 5 g
EUR 1198.8
Description: Diphenylpyraline is a first-generation antihistamine with anticholinergic effects of the diphenylpiperidine class.

Doxapram HCl
A8419-5.1 10 mM (in 1mL DMSO)
EUR 170.4
Description: Doxapram HCl is a respiratory stimulant.

Doxapram HCl
A8419-50 50 mg
EUR 157.2
Description: Doxapram HCl is a respiratory stimulant.

Doxycycline HCl
A8420-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Doxycycline Hydrochloride is a synthetic tetracycline derivative with similar antimicrobial activity.Doxycycline is a tetracycline antibiotic which is commonly used to treat a variety of infections. Doxycycline treatment resulted in a 96% loss of Wolbachi

Doxycycline HCl
A8420-50 50 mg
EUR 157.2
Description: Doxycycline Hydrochloride is a synthetic tetracycline derivative with similar antimicrobial activity.Doxycycline is a tetracycline antibiotic which is commonly used to treat a variety of infections. Doxycycline treatment resulted in a 96% loss of Wolbachi

Duloxetine HCl
A8421-10 10 mg
EUR 166.8
Description: Duloxetine HCl is a selective serotonin and norepinephrine reuptake inhibitor .

Duloxetine HCl
A8421-100 100 mg
EUR 808.8
Description: Duloxetine HCl is a selective serotonin and norepinephrine reuptake inhibitor .

Duloxetine HCl
A8421-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: Duloxetine HCl is a selective serotonin and norepinephrine reuptake inhibitor .

Ethambutol HCl
A8427-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: Nocodazole is a tubulin production inhibitor, also inhibits Abl, Abl(E255K) and Abl(T315I) with IC50 value of 0.21 ?M, 0.53 ?M and 0.64 ?M, respectively [1].Nocodazole is an inhibitor of microtubule polymerization which inhibits insulin-stimulated glucose transport.

Ethambutol HCl
A8427-50 50 mg
EUR 157.2
Description: Nocodazole is a tubulin production inhibitor, also inhibits Abl, Abl(E255K) and Abl(T315I) with IC50 value of 0.21 ?M, 0.53 ?M and 0.64 ?M, respectively [1].Nocodazole is an inhibitor of microtubule polymerization which inhibits insulin-stimulated glucose transport.

GW3965 HCl
A8444-10 10 mg
EUR 205.2
Description: GW3965 HCl is a selective, orally active non-steroidal agonist for the liver X receptor (LXR) [1].Nuclear receptors LXR? and LXR? have an important role in control of cholesterol and fatty acid metabolism in multiple cell types.

GW3965 HCl
A8444-5 5 mg
EUR 154.8
Description: GW3965 HCl is a selective, orally active non-steroidal agonist for the liver X receptor (LXR) [1].Nuclear receptors LXR? and LXR? have an important role in control of cholesterol and fatty acid metabolism in multiple cell types.

GW3965 HCl
A8444-5.1 10 mM (in 1mL DMSO)
EUR 199.2
Description: GW3965 HCl is a selective, orally active non-steroidal agonist for the liver X receptor (LXR) [1].Nuclear receptors LXR? and LXR? have an important role in control of cholesterol and fatty acid metabolism in multiple cell types.

GW3965 HCl
A8444-50 50 mg
EUR 614.4
Description: GW3965 HCl is a selective, orally active non-steroidal agonist for the liver X receptor (LXR) [1].Nuclear receptors LXR? and LXR? have an important role in control of cholesterol and fatty acid metabolism in multiple cell types.

Imidapril HCl
A8447-10 10 mg
EUR 129.6
Description: Imidapril (INN) is an ACE inhibitor used as an antihypertensive drug and for the treatment of chronic heart failure.

Imidapril HCl
A8447-5.1 10 mM (in 1mL DMSO)
EUR 151.2
Description: Imidapril (INN) is an ACE inhibitor used as an antihypertensive drug and for the treatment of chronic heart failure.

Imidapril HCl
A8447-50 50 mg
EUR 274.8
Description: Imidapril (INN) is an ACE inhibitor used as an antihypertensive drug and for the treatment of chronic heart failure.

Noscapine HCl
A8479-1000 1 g
EUR 517.2
Description: Noscapine hydrochloride is the hydrochloride form of Noscapine. Noscapine is an opioid alkaloid with several actions. Antagonist at Bradykinin B Receptor (bradykinin receptors) , inhibits carbachol-stimulated phosphoinositol turnover and enhances forskolin-stimulated cAMP increases in CNS tissues.

Noscapine HCl
A8479-10000 10 g
EUR 1783.2
Description: Noscapine hydrochloride is the hydrochloride form of Noscapine. Noscapine is an opioid alkaloid with several actions. Antagonist at Bradykinin B Receptor (bradykinin receptors) , inhibits carbachol-stimulated phosphoinositol turnover and enhances forskolin-stimulated cAMP increases in CNS tissues.

Noscapine HCl
A8479-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Noscapine hydrochloride is the hydrochloride form of Noscapine. Noscapine is an opioid alkaloid with several actions. Antagonist at Bradykinin B Receptor (bradykinin receptors) , inhibits carbachol-stimulated phosphoinositol turnover and enhances forskolin-stimulated cAMP increases in CNS tissues.

Noscapine HCl
A8479-5000 5 g
EUR 1198.8
Description: Noscapine hydrochloride is the hydrochloride form of Noscapine. Noscapine is an opioid alkaloid with several actions. Antagonist at Bradykinin B Receptor (bradykinin receptors) , inhibits carbachol-stimulated phosphoinositol turnover and enhances forskolin-stimulated cAMP increases in CNS tissues.

Thioridazine HCl
A8537-1000 1 g
EUR 226.8
Description: Thioridazine·HCl is a calcium channel protein inhibitor as well as D2DR/D4DR inhibitor. Its administration has been associated with hypotension. It has also been, after chronic treatment, used to test increased sensitivity of dopaminergic agents.

Thioridazine HCl
A8537-5 5 mg
EUR 129.6
Description: Thioridazine·HCl is a calcium channel protein inhibitor as well as D2DR/D4DR inhibitor. Its administration has been associated with hypotension. It has also been, after chronic treatment, used to test increased sensitivity of dopaminergic agents.

Thioridazine HCl
A8537-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: Thioridazine·HCl is a calcium channel protein inhibitor as well as D2DR/D4DR inhibitor. Its administration has been associated with hypotension. It has also been, after chronic treatment, used to test increased sensitivity of dopaminergic agents.

SRT1720 HCl
A4180-10 10 mg
EUR 309.6
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

SRT1720 HCl
A4180-200 200 mg
EUR 1730.4
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

SRT1720 HCl
A4180-5 5 mg
EUR 212.4
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

SRT1720 HCl
A4180-5.1 10 mM (in 1mL DMSO)
EUR 226.8
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

SRT1720 HCl
A4180-50 50 mg
EUR 825.6
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

SRT1720 HCl
A4180-S Evaluation Sample
EUR 97.2
Description: SRT1720 is a small-molecule compound which has the ability of activating the sirtuin subtype SIRT1 in vitro. The activity of SRT1720 as a SIRT1 activator is stronger than that of resveratrol.

Rosiglitazone HCl
A4310-100 100 mg
EUR 157.2
Description: Rosiglitazone is a blood glucose-lowering drugs, stimulating insulin secretion by binding to the PPAR receptors in fat cells.

Rosiglitazone HCl
A4310-200 200 mg
EUR 212.4
Description: Rosiglitazone is a blood glucose-lowering drugs, stimulating insulin secretion by binding to the PPAR receptors in fat cells.

Rosiglitazone HCl
A4310-25 25 mg
EUR 129.6
Description: Rosiglitazone is a blood glucose-lowering drugs, stimulating insulin secretion by binding to the PPAR receptors in fat cells.

Pioglitazone HCl
A4324-10 10 mg
EUR 142.8
Description: Pioglitazone HCl is a potent and highly selective agonist of PPAR? with IC50 value of 3?M[1].Pioglitazone HCl can increase both insulin-stimulated glucose uptake in peripheral tissues and insulin sensitivity in hepatic and adipose tissue.

Pioglitazone HCl
A4324-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Pioglitazone HCl is a potent and highly selective agonist of PPAR? with IC50 value of 3?M[1].Pioglitazone HCl can increase both insulin-stimulated glucose uptake in peripheral tissues and insulin sensitivity in hepatic and adipose tissue.

Pioglitazone HCl
A4324-50 50 mg
EUR 199.2
Description: Pioglitazone HCl is a potent and highly selective agonist of PPAR? with IC50 value of 3?M[1].Pioglitazone HCl can increase both insulin-stimulated glucose uptake in peripheral tissues and insulin sensitivity in hepatic and adipose tissue.

Anagrelide HCl
A4352-10 10 mg
EUR 122.4
Description: Anagrelide is a selective thrombocytopenic agent [1].Anagrelide is a FDA-approved drug for the treatment of essential thrombocythemia. It is originally identified as a potential inhibitor of platelet aggregation.

Anagrelide HCl
A4352-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Anagrelide is a selective thrombocytopenic agent [1].Anagrelide is a FDA-approved drug for the treatment of essential thrombocythemia. It is originally identified as a potential inhibitor of platelet aggregation.

Anagrelide HCl
A4352-50 50 mg
EUR 282
Description: Anagrelide is a selective thrombocytopenic agent [1].Anagrelide is a FDA-approved drug for the treatment of essential thrombocythemia. It is originally identified as a potential inhibitor of platelet aggregation.

Dorzolamide HCl
A4357-10 10 mg
EUR 153.6
Description: Dorzolamide HCl is a carbonic anhydrase inhibitor.

Dorzolamide HCl
A4357-100 100 mg
EUR 522
Description: Dorzolamide HCl is a carbonic anhydrase inhibitor.

Dorzolamide HCl
A4357-25 25 mg
EUR 205.2
Description: Dorzolamide HCl is a carbonic anhydrase inhibitor.

Dorzolamide HCl
A4357-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Dorzolamide HCl is a carbonic anhydrase inhibitor.

Dorzolamide HCl
A4357-50 50 mg
EUR 338.4
Description: Dorzolamide HCl is a carbonic anhydrase inhibitor.

Daunorubicin HCl
ADC-P-080 unit Ask for price

Metomidate HCL
50R-R7315 50 mg
EUR 211.2
Description: Metomidate HCL chemical reference substance

Granisetron HCl
A1295-100 100 mg
EUR 226.8
Description: 5-HT3 receptor antagonist that possesses potent antiemetic activity.

Granisetron HCl
A1295-5 5 mg
EUR 129.6
Description: 5-HT3 receptor antagonist that possesses potent antiemetic activity.

Granisetron HCl
A1295-5.1 10 mM (in 1mL DMSO)
EUR 142.8
Description: 5-HT3 receptor antagonist that possesses potent antiemetic activity.

Granisetron HCl
A1295-50 50 mg
EUR 157.2
Description: 5-HT3 receptor antagonist that possesses potent antiemetic activity.

Gemcitabine HCl
A1402-100 100 mg
EUR 129.6
Description: Gemcitabine HCl is an inhibitor of DNA synthesis with the IC50 value of 240.4±29.0 ?M (CCRF-CEM/dCK-/- cells), 14.7±2.8 nM (TC-1 cells), 36.7 ± 5.1 ?M (TC-1-GR cells), and 50 nM (PANC1 cells).

Gemcitabine HCl
A1402-5.1 10 mM (in 1mL DMSO)
EUR 129.6
Description: Gemcitabine HCl is an inhibitor of DNA synthesis with the IC50 value of 240.4±29.0 ?M (CCRF-CEM/dCK-/- cells), 14.7±2.8 nM (TC-1 cells), 36.7 ± 5.1 ?M (TC-1-GR cells), and 50 nM (PANC1 cells).

ADL5859 HCl
A2986-100 100 mg
EUR 1423.2
Description: Selective ? opioid receptor agonists are promising potential therapeutic agents for the treatment of various types of pain conditions. A spirocyclic derivative was identified as a promising hit through screening.

ADL5859 HCl
A2986-25 25 mg
EUR 588
Description: Selective ? opioid receptor agonists are promising potential therapeutic agents for the treatment of various types of pain conditions. A spirocyclic derivative was identified as a promising hit through screening.

ADL5859 HCl
A2986-5 5 mg
EUR 226.8
Description: Selective ? opioid receptor agonists are promising potential therapeutic agents for the treatment of various types of pain conditions. A spirocyclic derivative was identified as a promising hit through screening.

ADL5859 HCl
A2986-5.1 10 mM (in 1mL DMSO)
EUR 261.6
Description: Selective ? opioid receptor agonists are promising potential therapeutic agents for the treatment of various types of pain conditions. A spirocyclic derivative was identified as a promising hit through screening.

Puromycin HCl
20-abx076662
  • EUR 526.80
  • EUR 276.00
  • 250 mg
  • 50 mg

Nicardipine HCl
20-abx076668
  • EUR 360.00
  • EUR 276.00
  • 250 mg
  • 50 mg

Ambroxol HCl
20-abx076696
  • EUR 376.80
  • EUR 309.60
  • 500 mg
  • 50 mg

Irinotecan HCl
20-abx076771
  • EUR 861.60
  • EUR 376.80
  • 250 mg
  • 50 mg

Tetracyclin Hcl
abx082256-5g 5 g
EUR 226.8

Guanidine Hcl
abx082517-500g 500 g
EUR 226.8

Tetracyclin Hcl
abx082590-5g 5 g
EUR 210

EDC-HCl
20-abx095087
  • EUR 610.80
  • EUR 444.00
  • 1 kg
  • 500 g

Verapamil HCl
20-abx076503
  • EUR 260.40
  • EUR 360.00
  • 1 g
  • 5 g

Duloxetine HCl
20-abx076532
  • EUR 292.80
  • EUR 543.60
  • 10 mg
  • 50 mg

Ondansetron HCl
A5166-10 10 mg
EUR 129.6
Description: Ondansetron hydrochloride dihydrate is a serotonin-3 (5-HT3) receptor antagonist.

Ondansetron HCl
A5166-5.1 10 mM (in 1mL DMSO)
EUR 157.2
Description: Ondansetron hydrochloride dihydrate is a serotonin-3 (5-HT3) receptor antagonist.

Ondansetron HCl
A5166-50 50 mg
EUR 177.6
Description: Ondansetron hydrochloride dihydrate is a serotonin-3 (5-HT3) receptor antagonist.
Scroll to Top