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Proteases

Proteases is a general term for a class of enzymes that hydrolyze protein peptide chains. According to the way they degrade polypeptides, they are divided into two categories: endopeptidases and telopeptidases. The former can cut the large molecular weight polypeptide chain from the middle to form prions and peptones with smaller molecular weights; the latter can be divided into carboxypeptidase and aminopeptidase, which respectively remove the peptide from the free carboxyl terminus or free amino terminus of the polypeptide one by one. Chain hydrolysis produces amino acids.

A general term for a class of enzymes that hydrolyze peptide bonds in proteins. According to the way they hydrolyze polypeptides, they can be divided into endopeptidases and exopeptidases. Endopeptidase cleaves the interior of the protein molecule to form smaller molecular weight peptones and peptones. Exopeptidase hydrolyzes peptide bonds one by one from the end of the free amino group or carboxyl group of protein molecules, and frees amino acids, the former is aminopeptidase and the latter is carboxypeptidase. Proteases can be classified into serine proteases, sulfhydryl proteases, metalloproteases and aspartic proteases according to their active centers and optimum pH. According to the optimum pH value of its reaction, it is divided into acidic protease, neutral protease and alkaline protease. The proteases used in industrial production are mainly endopeptidases.

Proteases are widely found in animal offal, plant stems and leaves, fruits and microorganisms. Microbial proteases are mainly produced by molds and bacteria, followed by yeast and actinomycetes.

Enzymes that catalyze the hydrolysis of proteins. There are many kinds, the important ones are pepsin, trypsin, cathepsin, papain and subtilisin. Proteases have strict selectivity for the reaction substrates they act on. A protease can only act on certain peptide bonds in protein molecules, such as the peptide bonds formed by the hydrolysis of basic amino acids catalyzed by trypsin. Proteases are widely distributed, mainly in the digestive tract of humans and animals, and are abundant in plants and microorganisms. Due to limited animal and plant resources, the industrial production of protease preparations is mainly prepared by fermentation of microorganisms such as Bacillus subtilis and Aspergillus terrestris.

Targets for  Proteases

Products for  Proteases

  1. Cat.No. Nom du produit Informations
  2. GC49118 10-hydroxy Warfarin A metabolite of (R)-warfarin 10-hydroxy Warfarin  Chemical Structure
  3. GC33800 10Z-Nonadecenoic acid L'acide 10Z-nonadécénoÏque est une sorte d'acide gras À longue chaÎne ayant une activité anti-tumorale. 10Z-Nonadecenoic acid  Chemical Structure
  4. GC40368 11(R)-HEPE 11(R)-HEPE is produced by the oxidation of EPA by 11(R)-LO. 11(R)-HEPE  Chemical Structure
  5. GC40445 11(R)-HETE 11(R)-HETE is biosynthesized by 11(R)-LOs of the sea urchin, S. 11(R)-HETE  Chemical Structure
  6. GC39223 11-Beta-hydroxyandrostenedione La 11-bêta-hydroxyandrostènedione (4-androsten-11β-ol-3,17-dione) est un stéroÏde principalement présent dans l'origine surrénalienne (la 11β-hydroxylase est présente dans le tissu surrénal, mais absente dans le tissu ovarien). 11-Beta-hydroxyandrostenedione  Chemical Structure
  7. GC40730 11-cis Vaccenyl Acetate L'acétate de vaccényle 11-cis est un lipide spécifique aux mâles qui médie le comportement d'agrégation chez les mouches mâles et femelles, ce qui active quelques dizaines de neurones olfactifs situés dans la sensille T1 sur l'antenne des mouches mâles et femelles. 11-cis Vaccenyl Acetate  Chemical Structure
  8. GC40394 11-deoxy Corticosterone

    11-désoxy Corticostérone est une hormone stéroïde produite par la glande surrénale qui possède une activité minéralocorticoïde et agit comme précurseur de l'aldostérone.

    11-deoxy Corticosterone  Chemical Structure
  9. GC10821 11-keto-β-Boswellic Acid L'acide 11-céto-bêta-boswellique (11-céto-β -acide boswellique) est un acide triterpénique pentacyclique de la résine d'oléogume de l'écorce de l'arbre dentelé Boswellia, populairement connu sous le nom d'encens indien. L'acide 11-céto-bêta-boswellique a une activité anti-inflammatoire principalement due À l'inhibition de la 5-lipoxygénase (5-LOX) et de l'activation ultérieure des leucotriènes et du facteur nucléaire kappa B (NF-κ B) et de la génération alpha du facteur de nécrose tumorale production. 11-keto-β-Boswellic Acid  Chemical Structure
  10. GC61538 11-Oxo etiocholanolone 11-Oxo étiocholanolone (11-Ketoetiocholanolone) est un métabolite de l'étiocholanolone. 11-Oxo etiocholanolone  Chemical Structure
  11. GC41144 11-trans Leukotriene C4 11-trans Leukotriene C4 (11-trans LTC4) is a C-11 double bond isomer of LTC4. 11-trans Leukotriene C4  Chemical Structure
  12. GC41147 11-trans Leukotriene D4 11-trans Leukotriene D4 (11-trans LTD4) is a C-11 double bond isomer of LTD4. 11-trans Leukotriene D4  Chemical Structure
  13. GC41149 11-trans Leukotriene E4 Le 11-trans leucotriène E4 est un isomère du leucotriène E4 (LTE4). 11-trans Leukotriene E4  Chemical Structure
  14. GC63796 116-9e 116-9e (MAL2-11B) est un inhibiteur de l'ADNJA1 co-chaperon Hsp70. 116-9e  Chemical Structure
  15. GC34016 11beta-Hydroxyprogesterone (11β-Hydroxyprogesterone) La 11bêta-hydroxyprogestérone (11&bêta ;-hydroxyprogestérone) est un puissant inhibiteur de la 11β ;-hydroxystéroÏde déshydrogénase ; active également le récepteur minéralocorticoÏde humain dans les cellules COS-7 avec une DE50 de 10 nM. 11beta-Hydroxyprogesterone (11β-Hydroxyprogesterone)  Chemical Structure
  16. GC40447 12(R)-HETE Biosynthesis of 12(R)-HETE in invertebrates is via lipoxygenation of arachidonic acid. 12(R)-HETE  Chemical Structure
  17. GC40371 12(S)-HEPE 12(S)-HEPE is a monohydroxy fatty acid synthesized from EPA by the action of 12-LO. 12(S)-HEPE  Chemical Structure
  18. GC40448 12(S)-HETE

    12(S)-HETE is the predominant lipoxygenase product of mammalian platelets.

    12(S)-HETE  Chemical Structure
  19. GC41882 12(S)-HETrE 12(S)-HETrE is produced by 12-lipoxygenase oxidation of dihomo-γ-linolenic acid (DGLA). 12(S)-HETrE  Chemical Structure
  20. GC41095 12(S)-HpEPE

    12(S)-HpEPE is a monohydroperoxy polyunsaturated fatty acid produced by the action of 12-lipoxygenase on eicosapentaenoic acid.

    12(S)-HpEPE  Chemical Structure
  21. GC41122 12(S)-HpETE 12(S)-HpETE is a monohydroperoxy polyunsaturated fatty acid (PUFA) produced by the action of platelet or leukocyte 12-lipoxygenase (12-LO) on arachidonic acid. 12(S)-HpETE  Chemical Structure
  22. GC41123 12-epi Leukotriene B4 Leukotriene B4 (LTB4) compounds are produced by both enzymatic and non-enzymatic processes. 12-epi Leukotriene B4  Chemical Structure
  23. GC45962 12-hydroxy Lauric Acid L'acide 12-hydroxylaurique est un métabolite endogène. 12-hydroxy Lauric Acid  Chemical Structure
  24. GC60443 12-Ketodeoxycholic acid L'acide 12-cétodésoxycholique est un acide biliaire, métabolite du rein. 12-Ketodeoxycholic acid  Chemical Structure
  25. GC41096 12-oxo Leukotriene B4 Leukotriene B4 (LTB4) is a dihydroxy fatty acid derived from arachidonic acid through the 5-LO pathway. 12-oxo Leukotriene B4  Chemical Structure
  26. GC46418 12-oxo-13-HOME An oxylipin 12-oxo-13-HOME  Chemical Structure
  27. GC40372 12-OxoETE 12-OxoETE is synthesized by human platelets and Aplysia nervous tissue after incubation with arachidonic acid. 12-OxoETE  Chemical Structure
  28. GC19462 13(R)-HODE 13(R)-HODE is the opposite enantiomer of the 13(S)-HODE produced when linoleic acid is incubated with soybean lipoxygenase. 13(R)-HODE  Chemical Structure
  29. GC19463 13(S)-HODE 13(S)-HODE (13(S)-HODE), le produit du métabolisme de la 15-lipoxygénase (15-LOX) de l'acide linoléique, fonctionne comme le ligand endogène pour activer PPARγ. 13(S)-HODE  Chemical Structure
  30. GC41220 13(S)-HODE methyl ester 13(S)-hydroxyoctadecadienoic acid (13(S)-HODE) is a 15-lipoxygenase metabolite of linoleic acid produced in endothelial cells, leukocytes, and tumor cells. 13(S)-HODE methyl ester  Chemical Structure
  31. GC41896 13(S)-HODE-biotin 13(S)-HODE is the lipoxygenase metabolite of linoleic acid. 13(S)-HODE-biotin  Chemical Structure
  32. GC46420 13(S)-HODE-d4 An internal standard for the quantification of 13-HODE 13(S)-HODE-d4  Chemical Structure
  33. GC41897 13(S)-HOTrE 13(S)-HOTrE is the 15-lipoxygenase (15-LO) product of linolenic acid. 13(S)-HOTrE  Chemical Structure
  34. GC41898 13(S)-HOTrE(γ) 13(S)-HOTrE(γ) is the 15-LO product of γ-linolenic acid. 13(S)-HOTrE(γ)  Chemical Structure
  35. GC19474 13(S)-HpODE 13(S)-HpODE is produced by the oxidation of linoleic acid by lipoxygenase-1 (LO-1) in many plants including soybean, flaxseed, apples, and tea leaves,1,2 and by 15-LO in mammals. 13(S)-HpODE  Chemical Structure
  36. GC41899 13(S)-HpOTrE

    13(S)-HpOTrE is a monohydroperoxy polyunsaturated fatty acid produced in soybeans by the action of soybean LO-2 on esterified α-linolenic acid.

    13(S)-HpOTrE  Chemical Structure
  37. GC41900 13(S)-HpOTrE(γ) 13(S)-HpOTrE(γ) is a monohydroxy PUFA produced by the action of soybean lipoxygenase-1 (LO-1) on γ-linolenic acid. 13(S)-HpOTrE(γ)  Chemical Structure
  38. GC62758 13-cis-Vitamin A palmitate Le palmitate de 13-cis-vitamine A (palmitate de 13-cis-rétinyle) est un isomère 13-cis formé par le palmitate de vitamine A dans les flocons de maÏs. 13-cis-Vitamin A palmitate  Chemical Structure
  39. GC41911 13-epi-12-oxo Phytodienoic Acid 13-epi-12-oxo Phytodienoic acid (13-epi-12-oxo PDA) is a lipoxygenase metabolite of α-linolenic acid in the leaves of green plants such as corn. 13-epi-12-oxo Phytodienoic Acid  Chemical Structure
  40. GC49759 13C17-Mycophenolic Acid An internal standard for the quantification of mycophenolic acid 13C17-Mycophenolic Acid  Chemical Structure
  41. GC41206 14(S)-HDHA La 14(S)-HDHA (14(S)-HDoHE) est un produit d'oxygénation de l'acide docosahexaénoÏque (DHA). 14(S)-HDHA  Chemical Structure
  42. GC41100 14,15-dehydro Leukotriene B4 Leukotriene B4 (LTB4) is a dihydroxy fatty acid derived from arachidonic acid through the 5-lipoxygenase pathway. 14,15-dehydro Leukotriene B4  Chemical Structure
  43. GC41145 14,15-Leukotriene C4 Leukotrienes (LTs) are a group of acute inflammatory mediators derived from arachidonic acid in leukocytes. 14,15-Leukotriene C4  Chemical Structure
  44. GC41148 14,15-Leukotriene D4 14,15-Leukotriene D4 (14,15-LTD4) is a member of an alternate class of LTs synthesized by a pathway involving the dual actions of 15- and 12-lipoxygenases (15- and 12-LOs) on arachidonic acid via 15-HpETE and 14,15-LTA4 intermediates. 14,15-Leukotriene D4  Chemical Structure
  45. GC41150 14,15-Leukotriene E4 Leukotrienes (LTs) are a group of acute inflammatory mediators derived from arachidonic acid in leukocytes. 14,15-Leukotriene E4  Chemical Structure
  46. GC41415 15(R)-Lipoxin A4

    Lipid-derived lipoxins are produced at the site of vascular and mucosal inflammation where they down-regulate polymorphonuclear leukocyte recruitment and function.

    15(R)-Lipoxin A4  Chemical Structure
  47. GC40427 15(S)-HEDE 15(S)-HEDE is produced from 11Z,14Z-eicosadienoic acid by 15-LO. 15(S)-HEDE  Chemical Structure
  48. GC40373 15(S)-HEPE 15(S)-HEPE is a monohydroxy fatty acid synthesized from EPA by the action of 15-LO. 15(S)-HEPE  Chemical Structure
  49. GC40451 15(S)-HETE 15(S)-HETE is a major arachidonic acid metabolite from the 15-lipoxygenase pathway. 15(S)-HETE  Chemical Structure
  50. GC41925 15(S)-HETE Ethanolamide Arachidonoyl ethanolamide was the first endogenous cannabinoid (CB) to be isolated and characterized as an agonist acting on the same receptors (CB1 and CB2) as THC. 15(S)-HETE Ethanolamide  Chemical Structure
  51. GC40839 15(S)-HETE methyl ester 15(S)-HETE methyl ester is a synthetic derivative of 15(S)-HETE, a major arachidonic acid metabolite from the 15-lipoxygenase pathway. 15(S)-HETE methyl ester  Chemical Structure
  52. GC46442 15(S)-HETE-d8 An internal standard for the quantification of 15-HETE 15(S)-HETE-d8  Chemical Structure
  53. GC49894 15(S)-HETE-d8 ethyl ester An internal standard for the quantification of 15(S)-HETE ethyl ester 15(S)-HETE-d8 ethyl ester  Chemical Structure
  54. GC41927 15(S)-HETrE 15(S)-HETrE is the hydroxy-trienoic acid resulting from 15-lipoxygenation of dihomo-γ-linolenic acid. 15(S)-HETrE  Chemical Structure
  55. GC41403 15(S)-HpEDE

    15(S)-HpEDE is a monohydroperoxy polyunsaturated fatty acid produced by the action of 15-lipoxygenase on eicosadienoic acid.

    15(S)-HpEDE  Chemical Structure
  56. GC41101 15(S)-HpEPE

    15(S)-HpEPE is a monohydroperoxy polyunsaturated fatty acid produced by the action of 15-lipoxygenase on eicosapentaenoic acid.

    15(S)-HpEPE  Chemical Structure
  57. GC41124 15(S)-HpETE

    15(S)-HpETE is a monohydroperoxy polyunsaturated fatty acid (PUFA) produced by the action of 15-lipoxygenase (15-LO) on arachidonic acid.

    15(S)-HpETE  Chemical Structure
  58. GC11988 15-acetoxy Scirpenol Le 15-acétoxyscirpénol, l'une des mycotoxines du groupement acétoxyscirpénol (ASM), induit fortement l'apoptose et inhibe la croissance des lymphocytes T Jurkat de manière dose-dépendante en activant d'autres caspases indépendantes de la caspase-3. 15-acetoxy Scirpenol  Chemical Structure
  59. GC19442 15-Acetyldeoxy Nivalenol Le 15-acétyldésoxy nivalénol est un trichothécène hautement toxique présent dans les céréales, et un métabolite du désoxynivalénol, présente une toxicité pour les cellules HepG2. 15-Acetyldeoxy Nivalenol  Chemical Structure
  60. GC41937 15-keto-17-phenyl trinor Prostaglandin F2α ethyl amide Bimatoprost is the Allergan trade name for 17-phenyl trinor prostaglandin F2α ethyl amide (17-phenyl trinor PGF2α ethyl amide), an F-series PG analog which has been approved for use as an ocular hypotensive drug. 15-keto-17-phenyl trinor Prostaglandin F2α ethyl amide  Chemical Structure
  61. GC41938 15-Lipoxygenase Inhibitor 1 L'inhibiteur de 15-lipoxygénase 1 est un inhibiteur sélectif de la 15-lipoxygénase, avec une CI50 de 18 μM. L'inhibiteur de la 15-lipoxygénase 1 a des CI50 de 19,5 μM et 19,1 μM pour la 15-lipoxygénase de soja (SLO) et la 15-lipoxygénase-1 humaine (15-LOX-1), respectivement. L'inhibiteur de la 15-lipoxygénase 1 a un potentiel pour la recherche sur le cancer de la prostate. 15-Lipoxygenase Inhibitor 1  Chemical Structure
  62. GC41940 15-OxoEDE 15-OxoEDE is produced by the oxidation of 15-HEDE. 15-OxoEDE  Chemical Structure
  63. GC40376 15-OxoETE 15-OxoETE is produced by oxidation of the 15-hydroxyl of 15-HETE. 15-OxoETE  Chemical Structure
  64. GC41309 16α-hydroxy Prednisolone 16α-hydroxy Prednisolone est un métabolite stéréosélectif de l'épimère 22(R) du budésonide glucocorticoÏde via les enzymes du cytochrome P450 3A (CYP3A). 16α-hydroxy Prednisolone  Chemical Structure
  65. GC35058 16-Dehydroprogesterone La 16-déhydroprogestérone est un progestatif stéroïdien. 16-Dehydroprogesterone  Chemical Structure
  66. GC46451 16F16 A PDI inhibitor 16F16  Chemical Structure
  67. GC45909 17α-hydroxy Pregnenolone 1α-hydroxy Pregnenolone est un stéroÏde pregnane. 17α-hydroxy Pregnenolone  Chemical Structure
  68. GC41300 17β-hydroxy Exemestane 17β-hydroxy Exemestane is the primary active metabolite of exemestane. 17β-hydroxy Exemestane  Chemical Structure
  69. GC41951 17(R)-Resolvin D1

    Resolvins are a family of potent lipid mediators derived from both eicosapentaenoic acid and docosahexaenoic acid.

    17(R)-Resolvin D1  Chemical Structure
  70. GC41227 17(R)-Resolvin D1 methyl ester 17(R)-Resolvin D1 (17(R)-RvD1) is an aspirin-triggered epimer of RvD1 that reduces human polymorphonuclear leukocyte transendothelial migration, the earliest event in acute inflammation, with equipotency to RvD1 (EC50 = ~30 nM). 17(R)-Resolvin D1 methyl ester  Chemical Structure
  71. GC41952 17(R)-Resolvin D4 17(R)-Resolvin D4 (17(R)-RvD4) is an aspirin-triggered epimer of RvD4 . 17(R)-Resolvin D4  Chemical Structure
  72. GC41208 17(S)-HDHA 17(S)-HDHA is a primary mono-oxygenation product of docosahexaenoic acid in human whole blood, human leukocytes, and mouse brain. 17(S)-HDHA  Chemical Structure
  73. GC49356 17(S)-HDoTE A metabolite of adrenic acid 17(S)-HDoTE  Chemical Structure
  74. GC40975 17(S)-HpDHA 17(S)-HpDHA is a mono-oxygenation product of docosahexaenoic acid in human whole blood, human leukocytes, human glial cells, and mouse brain. 17(S)-HpDHA  Chemical Structure
  75. GC11720 17-AAG (KOS953) An inhibitor of Hsp90 17-AAG (KOS953)  Chemical Structure
  76. GC17210 17-AAG Hydrochloride Hsp90 inhibitor,geldanamycin analogue 17-AAG Hydrochloride  Chemical Structure
  77. GC41955 17-DMAG 17-DMAG (17-DMAG) est un puissant inhibiteur de Hsp90, se liant À Hsp90 avec une CE50 de 62 ± ; 29 nM. 17-DMAG  Chemical Structure
  78. GC13044 17-DMAG (Alvespimycin) HCl Le 17-DMAG (alvespimycine) HCl (chlorhydrate de 17-DMAG ; KOS-1022 ; BMS 826476) est un puissant inhibiteur de Hsp90, se liant À Hsp90 avec une EC50 de 62± ; 29 nM. 17-DMAG (Alvespimycin) HCl  Chemical Structure
  79. GC41529 17-oxo-4(Z),7(Z),10(Z),13(Z),15(E),19(Z)-Docosahexaenoic Acid 17-oxo-4(Z),7(Z),10(Z),13(Z),15(E),19(Z)-Docosahexaenoic acid is a metabolite of lipoxygenase-mediated oxidation of DHA that is produced endogenously by aspirin-enhanced COX-2 activity. 17-oxo-4(Z),7(Z),10(Z),13(Z),15(E),19(Z)-Docosahexaenoic Acid  Chemical Structure
  80. GC41209 17-oxo-7(Z),10(Z),13(Z),15(E),19(Z)-Docosapentaenoic Acid Docosapentaenoic acid (DPA) is a ω-3 fatty acid found in fish oils. 17-oxo-7(Z),10(Z),13(Z),15(E),19(Z)-Docosapentaenoic Acid  Chemical Structure
  81. GC68426 17a-Hydroxypregnenolone-d3 17a-Hydroxypregnenolone-d3  Chemical Structure
  82. GC35061 18α-Glycyrrhetinic acid 18α-L'acide glycyrrhétinique, un composé dérivé de l'alimentation, est un inhibiteur de NF-kB et un activateur du protéasome, qui sert de facteur de pro-longévité et d'anti-agrégation dans un organisme multicellulaire. 18α-Glycyrrhetinic acid  Chemical Structure
  83. GC41980 18-carboxy dinor Leukotriene B4 18-carboxy dinor Leukotriene B4 (18-carboxy dinor LTB4) is a β-oxidation metabolite of LTB4. 18-carboxy dinor Leukotriene B4  Chemical Structure
  84. GC33818 18-Hydroxycorticosterone La 18-hydroxycorticostérone est un corticostéroÏde et un dérivé de la corticostérone, qui peut entraÎner de graves déséquilibres électrolytiques. 18-Hydroxycorticosterone  Chemical Structure
  85. GC63603 19-Hydroxyandrost-4-ene-3,17-dione 19-Hydroxyandrost-4-ene-3,17-dione  Chemical Structure
  86. GC39296 1G244 1G244 est un puissant inhibiteur de DPP8/9 avec des IC50 de 12 nM et 84 nM, respectivement. 1G244 n'inhibe pas DPPIV et DPPII. 1G244 induit l'apoptose dans les cellules de myélome multiple et a des effets anti-myélome. 1G244  Chemical Structure
  87. GC38359 1H-pyrazole Le 1H-pyrazole est un métabolite endogène. 1H-pyrazole  Chemical Structure
  88. GC49823 2′-C-β-Methylguanosine An active nucleoside metabolite of BMS-986094 2′-C-β-Methylguanosine  Chemical Structure
  89. GC64738 2′-Deoxyadenosine 5′-monophosphate disodium &2#8242;-Déoxyadénosine 5′-monophosphate disodique, un dérivé de l'acide nucléique AMP, est un désoxyribonucléotide présent dans l'ADN. 2′-Deoxyadenosine 5′-monophosphate disodium  Chemical Structure
  90. GC62772 2’-Deoxyadenosine-5’-triphosphate trisodium &2rsquo;-Déoxyadénosine-5’-triphosphate trisodique (dATP trisodique) est un nucléotide utilisé dans les cellules pour la synthèse (ou la réplication) de l'ADN, en tant que substrat de l'ADN polymérase. 2’-Deoxyadenosine-5’-triphosphate trisodium  Chemical Structure
  91. GC62774 2’-Deoxyguanosine 5’-monophosphate disodium &2rsquo;-Deoxyguanosine 5’-monophosphate disodique (5′-dGMP disodique) est un mononucléotide ayant la guanine comme base nucléique. 2’-Deoxyguanosine 5’-monophosphate disodium  Chemical Structure
  92. GC46508 2',2'-Difluoro-2'-deoxyuridine An active metabolite of gemcitabine 2',2'-Difluoro-2'-deoxyuridine  Chemical Structure
  93. GC33622 2',4'-Dihydroxyacetophenone La 2',4'-dihydroxyacétophénone (résacétophénone) est une acétophénone portant des substituants hydroxy aux positions 2' et 4'. 2',4'-Dihydroxyacetophenone  Chemical Structure
  94. GC60462 2',4'-Dimethylacetophenone 2',4'-Dimethylacetophenone  Chemical Structure
  95. GC33605 2'-Deoxyadenosine monohydrate Le monohydrate de 2'-désoxyadénosine est un désoxyribonucléoside. 2'-Deoxyadenosine monohydrate  Chemical Structure
  96. GC38258 2'-Deoxyadenosine-5'-monophosphate Le 2′-désoxyadénosine 5′-monophosphate, un dérivé de l'acide nucléique AMP, est un désoxyribonucléotide présent dans l'ADN. 2'-Deoxyadenosine-5'-monophosphate  Chemical Structure
  97. GC42150 2'-Deoxycytidine 5'-diphosphate (sodium salt hydrate) 2'-Deoxycytidine-5'-diphosphate (dCDP) trisodique est un métabolite endogène. 2'-Deoxycytidine 5'-diphosphate (sodium salt hydrate)  Chemical Structure
  98. GC17436 2'-Deoxycytidine-5'-monophosphoric acid L'acide 2'-désoxycytidine-5'-monophosphorique est un métabolite endogène. 2'-Deoxycytidine-5'-monophosphoric acid  Chemical Structure
  99. GC48440 2'-Deoxycytidine-5'-triphosphate (sodium salt) 2'-Deoxycytidine-5'-triphosphate (sel de sodium) (dCTP sel trisodique) est un nucléoside triphosphate qui peut être utilisé pour la synthèse d'ADN. 2'-Deoxycytidine-5'-triphosphate (sodium salt)  Chemical Structure
  100. GC10897 2'-Deoxyguanosine La 2'-désoxyguanosine (désoxyguanosine) est composée de la guanine nucléoside purique liée par son azote N9 au carbone C1 du désoxyribose. 2'-Deoxyguanosine  Chemical Structure
  101. GC38191 2'-Deoxyguanosine monohydrate Le monohydrate de 2'-désoxyguanosine est un métabolite endogène. 2'-Deoxyguanosine monohydrate  Chemical Structure

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