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Startseite >> Signaling Pathways >> Cardiovascular >> Hypertension

Hypertension

Produkte für  Hypertension

  1. Bestell-Nr. Artikelname Informationen
  2. GC45200 α-CGRP (rat) (trifluoroacetate salt)

    Calcitonin Gene-Related Peptide-1 (rat), α-Calcitonin Gene-Related Peptide (rat), CGRP-1 (rat)

     α-Calcitonin gene-related peptide (α-CGRP) is a neuropeptide with roles in vasodilation, cardiovascular regulation, and inflammation. α-CGRP (rat) (trifluoroacetate salt) Chemical Structure
  3. GC48283 α-Linolenic Acid-d14

    ALAd14

     An internal standard for the quantification of αLinolenic acid α-Linolenic Acid-d14 Chemical Structure
  4. GC40105 βARK1 Inhibitor βARK1-Inhibitor (Methyl-5-[2-(5-nitro-2-furyl)vinyl]-2-furoat) ist ein GRK2 (β-ARK1)-Inhibitor. βARK1 Inhibitor Chemical Structure
  5. GC52404 γ-Glu-Phe (trifluoroacetate salt)

    γ-Glutamylphenylalanine

     A dipeptide with metabolism-altering activity γ-Glu-Phe (trifluoroacetate salt) Chemical Structure
  6. GC41661 (±)-4-hydroxy Propranolol β-D-Glucuronide (±)-4-hydroxy Propranolol β-D-glucuronide is a metabolite of (±)-4-hydroxy propranolol, which is a metabolite of propranolol. (±)-4-hydroxy Propranolol β-D-Glucuronide Chemical Structure
  7. GC46273 (±)-Atenolol-d7

    (R,S)-Atenolol-d7, Duraatenol, ICI 66082

     An internal standard for the quantification of (±)-atenolol (±)-Atenolol-d7 Chemical Structure
  8. GC46289 (±)-Felodipine-d5 An internal standard for the quantification of (±)-felodipine (±)-Felodipine-d5 Chemical Structure
  9. GC46304 (±)-Nebivolol-d4 (hydrochloride) A neuropeptide with diverse biological activities (±)-Nebivolol-d4 (hydrochloride) Chemical Structure
  10. GC46307 (±)-Propranolol-d7 An internal standard for the quantification of propranolol (±)-Propranolol-d7 Chemical Structure
  11. GC46312 (±)-Verapamil-d3 (hydrochloride)

    (±)-Verapamil-d3 hydrochloride; CP-16533-1-d3 hydrochloride

     A neuropeptide with diverse biological activities (±)-Verapamil-d3 (hydrochloride) Chemical Structure
  12. GC40268 (±)14(15)-DiHET

    (±)14,15DiHETrE

     Epoxide hydrolases convert the EETs into vicinal diols, with the concurrent loss of much of their biological activity. (±)14(15)-DiHET Chemical Structure
  13. GC40434 (±)16-HETE

    (±)16-Hydroxyeicosatetraenoic Acid

     Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. (±)16-HETE Chemical Structure
  14. GC40437 (±)5(6)-DiHET lactone

    (±)5,6DiHETrE lactone

     5,6-DiHET lactone is a lactonized form of 5,6-EET and 5,6-DiHET. (±)5(6)-DiHET lactone Chemical Structure
  15. GC41722 (R,S)-Carvedilol Glucuronide (R,S)-Carvedilol glucuronide is a racemic mixture of the carvedilol metabolites (R)-carvedilol glucuronide and (S)-carvedilol glucuronide. (R,S)-Carvedilol Glucuronide Chemical Structure
  16. GC18634 11-deoxy Prostaglandin E1

    11deoxy PGE1

     11-deoxy Prostaglandin E1 (11-deoxy PGE1) is a synthetic analog of PGE1. 11-deoxy Prostaglandin E1 Chemical Structure
  17. GC41401 11-deoxy Prostaglandin F1α

    11deoxy PGF1α

     11-deoxy PGF1α is a synthetic analog of PGF1α. 11-deoxy Prostaglandin F1α Chemical Structure
  18. GC41402 11-deoxy Prostaglandin F1β

    9β,11deoxy PGF1α, 11deoxy PGF1β

     11-deoxy PGF1β is a synthetic analog of PGF1β. 11-deoxy Prostaglandin F1β Chemical Structure
  19. GC46425 13,14-dihydro-15-keto Prostaglandin E1-d4

    13,14dh15k PGE1d4

     A neuropeptide with diverse biological activities 13,14-dihydro-15-keto Prostaglandin E1-d4 Chemical Structure
  20. GC41935 15-keto Treprostinil (sodium salt) 15-keto Treprostinil is an impurity found in treprostinil, which is a stable analog of prostaglandin I2 with a longer plasma half-life. 15-keto Treprostinil (sodium salt) Chemical Structure
  21. GC41159 16,16-dimethyl Prostaglandin D2

    16,16dimethyl PGD2

     16,16-dimethyl PGD2 is a metabolically stable synthetic analog of PGD2. 16,16-dimethyl Prostaglandin D2 Chemical Structure
  22. GC18635 18-hydroxy-11-deoxy Corticosterone

    18-Hydroxydeoxycorticosterone, 18-OH-DOC

     18-hydroxy-11-deoxy Corticosterone (18-OH-DOC) is a mineralocorticoid secreted by the zona fasciculata of the adrenal gland. 18-hydroxy-11-deoxy Corticosterone Chemical Structure
  23. GC52048 3-hydroxy-4-Methoxyphenethylamine (hydrochloride)

    4-O-methyl Dopamine, p-methoxy Dopamine, para-methoxy Dopamine, 4-methoxy-3-Hydroxyphenethylamine

     3-Hydroxy-4-Methoxyphenethylamin (Hydrochlorid) ist eine Katecholaminverbindung, die eine hemmende Wirkung auf die Dihydropteridinreduktase hat. 3-hydroxy-4-Methoxyphenethylamine (hydrochloride) Chemical Structure
  24. GC42409 4-hydroxy Nebivolol (hydrochloride) 4-hydroxy Nebivolol is a major metabolite of nebivolol. 4-hydroxy Nebivolol (hydrochloride) Chemical Structure
  25. GC42498 5-chloro Hydrochlorothiazide 5-chloro Hydrochlorothiazide is a derivative of hydrochlorothiazide, which is a diuretic and antihypertensive agent that increases renal excretion of sodium, potassium, chloride, and bicarbonate ions by inhibiting tubular reabsorptive mechanisms. 5-chloro Hydrochlorothiazide Chemical Structure
  26. GC41483 5-hydroxy Propranolol 5-hydroxy Propranolol is a metabolite of propranolol, a β-adrenergic receptor antagonist. 5-hydroxy Propranolol Chemical Structure
  27. GC42563 5-methyl-2-HOBA (hydrochloride)

    5-Me-2-HOBA, 5-methyl-2Hydroxybenzylamine

     5-methyl-2-HOBA is an isoketal scavenger. 5-methyl-2-HOBA (hydrochloride) Chemical Structure
  28. GC40338 9-deoxy-9-methylene Prostaglandin E2

    9deoxy9methylene PGE2

     9-deoxy-9-methylene Prostaglandin E2 (9-deoxy-9-methylene PGE2) is a stable, isosteric analog of PGE2. 9-deoxy-9-methylene Prostaglandin E2 Chemical Structure
  29. GC48486 AAA A GPR75 antagonist AAA Chemical Structure
  30. GC49406 ACT-373898 ACT-373898 ist ein inaktiver CarbonsÄuremetabolit von Macitentan. ACT-373898 Chemical Structure
  31. GC42738 Adrenomedullin (13-52) (human) (trifluoroacetate salt) Adrenomedullin (13-52) is a truncated form of adrenomedullin (1-52). Adrenomedullin (13-52) (human) (trifluoroacetate salt) Chemical Structure
  32. GC46820 AHU377-d4

    Sacubitril-d4

     AHU377-d4 (AHU-377-d4) ist das Deuterium mit der Bezeichnung Sacubitril. AHU377-d4 Chemical Structure
  33. GC49262 Alytesin (trifluoroacetate salt) A neuropeptide with diverse biological activities Alytesin (trifluoroacetate salt) Chemical Structure
  34. GC49638 Ambrisentan-d3 An internal standard for the quantification of ambrisentan Ambrisentan-d3 Chemical Structure
  35. GC46841 Amiloride (hydrochloride) (hydrate)

    MK-870

     A neuropeptide with diverse biological activities Amiloride (hydrochloride) (hydrate) Chemical Structure
  36. GC46845 Amlodipine-d4 (maleate) An internal standard for the quantification of amlodipine Amlodipine-d4 (maleate) Chemical Structure
  37. GC52415 Angiotensin A (trifluoroacetate salt)

    Ala-Arg-Val-Tyr-Ile-His-Pro-Phe, DesAsp1-Ala1-Ang II

     An AT1 and AT2 receptor agonist and active metabolite of angiotensin II Angiotensin A (trifluoroacetate salt) Chemical Structure
  38. GC48997 Argipressin (acetate)

    AVP, Arg8-Vasopressin

     A peptide hormone with vasoconstrictive and antidiuretic activities Argipressin (acetate) Chemical Structure
  39. GC39554 AT2 receptor agonist C21

    Compound 21

     AT2-Rezeptoragonist C21 ist ein wirkstoffÄhnlicher selektiver Angiotensin-II-AT2-Rezeptoragonist mit Ki-Werten von 0,4 nM und >10 μM fÜr den AT2-Rezeptor bzw. AT1-Rezeptor. AT2 receptor agonist C21 Chemical Structure
  40. GC42871 Atrial Natriuretic Peptide (1-28) (rat) (trifluoroacetate salt)

    ANF, ANP, Atrial Natriuretic Factor, α-Atriopeptin (rat)

     Atrial natriuretic peptide (ANP) is an endogenous peptide generated by proteolysis of prepro-ANP that is secreted by cardiomyocytes in the heart. Atrial Natriuretic Peptide (1-28) (rat) (trifluoroacetate salt) Chemical Structure
  41. GC42872 Atrial Natriuretic Peptide (3-28) (human) (trifluoroacetate salt)

    ANP (3-28) (human)

     Atrial natriuretic peptide (ANP) (3-28) is a synthetic and truncated form of ANP, which is an endogenous peptide generated by proteolysis of prepro-ANP that is secreted by cardiomyocytes in the heart. Atrial Natriuretic Peptide (3-28) (human) (trifluoroacetate salt) Chemical Structure
  42. GC45390 Benazepril Acyl-β-D-Glucuronide

    Benazapril Glucuronide

       Benazepril Acyl-β-D-Glucuronide Chemical Structure
  43. GC42913 Benazeprilat

    CGS 14831

     Benazeprilat ist ein oral wirksamer Wirkstoff und der aktive Metabolit von Benazepril, einem Carboxyl-haltigen ACE-Hemmer mit blutdrucksenkender Wirkung. Benazeprilat Chemical Structure
  44. GC42924 Beraprost (sodium salt)

    ML 1129, Procyclin, TRK 100

     Beraprost is an analog of prostacyclin in which the unstable enol-ether has been replaced by a benzofuran ether function. Beraprost (sodium salt) Chemical Structure
  45. GC42966 Bopindolol (malonate)

    (±)-Bopindolol (malonate)

     Bopindolol ((±)-Bopindolol)malonat ist ein oral aktiver Antagonist von β-Adrenozeptoren (ARs) mit partieller agonistischer AktivitÄt. Bopindolol (malonate) Chemical Structure
  46. GC49880 Bradykinin (trifluoroacetate salt) An endogenous vasodilator Bradykinin (trifluoroacetate salt) Chemical Structure
  47. GC52424 Bradykinin Fragment (1-5) (trifluoroacetate salt)

    Arg-Pro-Pro-Gly-Phe, BK1-5, RPPGF

     A metabolite of bradykinin Bradykinin Fragment (1-5) (trifluoroacetate salt) Chemical Structure
  48. GC45887 Bufuralol-d9 (hydrochloride) An internal standard for the quantification of bufuralol Bufuralol-d9 (hydrochloride) Chemical Structure
  49. GC43140 Captopril Disulfide

    SQ 14,551

     Captoprildisulfid ist ein Metabolit von Captopril mit blutdrucksenkender Wirkung. Captopril Disulfide Chemical Structure
  50. GC45398 Captopril-d3   Captopril-d3 Chemical Structure
  51. GC49564 Carazolol-d7

    (±)-Carazolol-d7

     An internal standard for the quantification of carazolol Carazolol-d7 Chemical Structure
  52. GC47045 Carvedilol-d5 An internal standard for the quantification of carvedilol Carvedilol-d5 Chemical Structure
  53. GC52006 CB-096 An inhibitor of RAN translation CB-096 Chemical Structure
  54. GC43247 Chlorthalidone Impurity G Chlorthalidone impurity G is a potential impurity found in commercial preparations of chlorthalidone that has moderate antihypertensive effects. Chlorthalidone Impurity G Chemical Structure
  55. GC43270 Ciprostene (calcium salt)

    Ciprostene calcium, U61431F

     Ciprostene is the 9β-methyl analog of carbaprostacyclin and a stable analog of PGI2. Ciprostene (calcium salt) Chemical Structure
  56. GC47100 Clevidipine-d7

    rac-Clevidipine-d7

     A neuropeptide with diverse biological activities Clevidipine-d7 Chemical Structure
  57. GC47103 Clonidine-d4 (hydrochloride) An internal standard for the quantification of clonidine Clonidine-d4 (hydrochloride) Chemical Structure
  58. GC47116 Coenzyme Q10-d6

    CoQ10-d6, Ubidecarenone-d6, Ubiquinone-10-d6, Ubiquinone Q10-d6

    Ein interner Standard zur Quantifizierung von CoQ10.

     Coenzyme Q10-d6 Chemical Structure
  59. GC47120 Conivaptan-d4 An internal standard for the quantification of conivaptan Conivaptan-d4 Chemical Structure
  60. GC47175 Deacetylforskolin

    7-Deactylcoleonol, Forskolin D

     A diterpene with diverse biological activities Deacetylforskolin Chemical Structure
  61. GC46126 Debrisoquin (hemisulfate)

    Isocaramidine sulfate, Ro 5-3307/1

     A post-ganglionic sympathetic blocker Debrisoquin (hemisulfate) Chemical Structure
  62. GC43399 Dehydro Amlodipine (fumarate) Dehydro amlodipine is a potential impurity found in commercial preparations of amlodipine. Dehydro Amlodipine (fumarate) Chemical Structure
  63. GC49866 Desmethyl Carvedilol

    BM 14242, O-desmethyl Carvedilol

     An active metabolite of carvedilol Desmethyl Carvedilol Chemical Structure
  64. GC49459 Desmopressin (trifluoroacetate salt)

    Adiuretin, DDAVP

     A vasopressin receptor agonist Desmopressin (trifluoroacetate salt) Chemical Structure
  65. GC62026 Devaleryl Valsartan Impurity

    Valsartan Impurity B

     Die Devaleryl-Valsartan-Verunreinigung ist ein Zwischenprodukt bei der Synthese von Valsartan. Devaleryl Valsartan Impurity Chemical Structure
  66. GC46131 Diazoxide-d3 An internal standard for the quantification of diazoxide Diazoxide-d3 Chemical Structure
  67. GC45427 Dihydrolycorine   Dihydrolycorine Chemical Structure
  68. GC49045 Dopastin

    NSC 252927

     A bacterial metabolite and an inhibitor of dopamine β-hydroxylase Dopastin Chemical Structure
  69. GC47268 Doxazosin-d8 (hydrochloride) An internal standard for the quantification of doxazosin Doxazosin-d8 (hydrochloride) Chemical Structure
  70. GC43601 Enalaprilat (hydrate) Angiotensin-converting enzyme (ACE) converts angiotensin I to angiotensin II, a peptide hormone that impacts vascular smooth muscle tone and renal salt exchange, driving hypertension. Enalaprilat (hydrate) Chemical Structure
  71. GC43608 Endothelin-3 (human, rat) (trifluoroacetate salt)

    ET-3

     Endothelin-3 is a peptide vasoconstricter and a ligand of the endothelin (ET) receptors ETA and ETB (Kbs = 1.05 and 1.49, respectively). Endothelin-3 (human, rat) (trifluoroacetate salt) Chemical Structure
  72. GC52035 Esmolol Acid (hydrochloride)

    ASL 8123

     An active metabolite of esmolol Esmolol Acid (hydrochloride) Chemical Structure
  73. GC47307 Esmolol-d7 (hydrochloride) An internal standard for the quantification of esmolol Esmolol-d7 (hydrochloride) Chemical Structure
  74. GC52303 Ethyl Mycophenolate A potential impurity found in commercial preparations of mycophenolate mofetil Ethyl Mycophenolate Chemical Structure
  75. GC60842 Finerenone

    BAY 94-8862

     FinerenoneFinerenone (BAY 94 - 8862) ist ein selektiver, oral aktives, nichtsteroid-Salz - Kortikosteroid-Rezeptor (MR) - Antagonist der dritten Generation mit einem IC50 von 18 nM. Finerenone Chemical Structure
  76. GC45761 Flupirtine-d4 (hydrochloride)

    D 9998-d4 hydrochloride

     Flupirtin-d4 (D 9998-d4) Hydrochlorid ist das mit Deuterium bezeichnete Flupirtin. Flupirtine-d4 (hydrochloride) Chemical Structure
  77. GC47371 Fosinopril-d7 (sodium salt) An internal standard for the quantification of fosinopril Fosinopril-d7 (sodium salt) Chemical Structure
  78. GC63298 Ganoderic acid N GanoderinsÄure N ist ein natÜrliches Terpenoid, das aus dem Pilz Ganoderma lucidum isoliert wurde. Ganoderic acid N Chemical Structure
  79. GC49117 Guanadrel Guanadrel ist ein oral aktiver postganglionÄrer adrenerger Inhibitor von Spiroketal. Guanadrel Chemical Structure
  80. GC47416 Guanfacine-13C,15N3 An internal standard for the quantification of guanfacine Guanfacine-13C,15N3 Chemical Structure
  81. GC45678 Guanoclor

    Guanochlor

     Guanoclor (Vatensol) ist ein Dopamin-Beta-Hydroxylase (DBH)-Hemmer, der die Noradrenalin-Synthese stÖrt. Guanoclor Chemical Structure
  82. GC46155 H-Ile-Pro-Pro-OH (trifluoroacetate salt)

    IPP

     A neuropeptide with diverse biological activities H-Ile-Pro-Pro-OH (trifluoroacetate salt) Chemical Structure
  83. GC47438 H-Val-Pro-Pro-OH (trifluoroactetate salt)

    VPP

     A neuropeptide with diverse biological activities H-Val-Pro-Pro-OH (trifluoroactetate salt) Chemical Structure
  84. GC43803 HA-1077 (hydrochloride)

    Fasudil

     Fasudil (HA-1077; AT877) dihydrochloride is a nonspecific RhoA/ROCK inhibitor and also has inhibitory effect on protein kinases, with an Ki of 0.33 μM for ROCK1, IC50s of 0.158 μM and 4.58 μM, 12.30 μ ;M, 1.650 μM fÜr ROCK2 bzw. PKA, PKC, PKG. HA-1077 (Hydrochlorid) ist auch ein potenter Ca2+-Kanalantagonist und Vasodilatator. HA-1077 (hydrochloride) Chemical Structure
  85. GC47439 Hydralazine-d4 (hydrochloride)

    1-Hydrazinophthalazine-d4

     A neuropeptide with diverse biological activities Hydralazine-d4 (hydrochloride) Chemical Structure
  86. GC47440 Hydrocortisone-d4

    Cortisol-d4

     An internal standard for the quantification of hydrocortisone Hydrocortisone-d4 Chemical Structure
  87. GC47441 Hydroflumethiazide-13C-d2

    Methforylthiazidine-13C,d2; Rontyl-13C,d2

     An internal standard for the quantification of hydroflumethiazide Hydroflumethiazide-13C-d2 Chemical Structure
  88. GC49250 Hydroxydehydro Nifedipine Carboxylate A metabolite of nifedipine Hydroxydehydro Nifedipine Carboxylate Chemical Structure
  89. GC43890 ICI 216140 Bombesin is a peptide, originally isolated from the skin of the European fire-bellied toad, with pressor and sympathoexcitatory activity. ICI 216140 Chemical Structure
  90. GC49195 Indapamide-13C-d3 An internal standard for the quantification of indapamide Indapamide-13C-d3 Chemical Structure
  91. GC49493 IRL 1620 (trifluoroacetate salt)

    PMZ-1620, SPI 1620, Suc-Glu9, Ala11,15-ET-1(8-21)

     A peptide ETB receptor agonist IRL 1620 (trifluoroacetate salt) Chemical Structure
  92. GC49343 Isoproterenol-d7 (hydrochloride)

    Isoprenaline-d7

     An internal standard for the quantification of isoproterenol Isoproterenol-d7 (hydrochloride) Chemical Structure
  93. GC52310 L-Arginine-13C6 (hydrochloride)

    L-(+)-Arginine-13C6

     An internal standard for the quantification of L-arginine L-Arginine-13C6 (hydrochloride) Chemical Structure
  94. GC49374 L-Arginine-d7 (hydrochloride)

    L-(+)-Arginine-d7

     L-Arginin-d7 ((S)-(+)-Arginin-d7) Hydrochlorid ist das mit Deuterium markierte L-Arginin-Hydrochlorid. L-Arginine-d7 (hydrochloride) Chemical Structure
  95. GC47534 Labetalol-d5 (hydrochloride)

    AH 5158A-d5, SCH 15719W-d5

     A neuropeptide with diverse biological activities Labetalol-d5 (hydrochloride) Chemical Structure
  96. GC45501 Lisinopril-d5   Lisinopril-d5 Chemical Structure
  97. GC52281 Losartan Azide A potential impurity in commercial preparations of losartan Losartan Azide Chemical Structure
  98. GC44112 Mabuterol Mabuterol is an agonist of the β2-adrenergic receptor (β2-AR). Mabuterol Chemical Structure
  99. GC47597 Manidipine-d4

    Franidipine-d4, (±)-Manidipine-d4

     An internal standard for the quantification of manidipine Manidipine-d4 Chemical Structure
  100. GC41639 Methyldopate

    αMethyldopa ethyl ester

     Methyldopat ist ein Ethylester-Prodrug von α-Methyldopa Methyldopate Chemical Structure
  101. GC46170 Methylspinazarin

    Methylspinazaline

     A bacterial metabolite and COMT inhibitor Methylspinazarin Chemical Structure

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