>> Signaling Pathways >> Proteases

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. 상품명 정보
  2. GC49118 10-hydroxy Warfarin A metabolite of (R)-warfarin 10-hydroxy Warfarin  Chemical Structure
  3. GC33800 10Z-Nonadecenoic acid 10Z-노나데센산은 항종양 활성이 있는 일종의 장쇄 지방산입니다. 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 11-베타-하이드록시안드로스텐디온(4-안드로스텐-11β-올-3,17-디온)은 주로 부신 기원에서 발견되는 스테로이드입니다(11β-하이드록실라제는 부신 조직에 존재하지만 난소 조직에는 존재하지 않음). 11-Beta-hydroxyandrostenedione  Chemical Structure
  7. GC40730 11-cis Vaccenyl Acetate 11-cis Vaccenyl Acetate는 수컷과 암컷 파리 모두에서 응집 행동을 매개하는 수컷 특이적 지질로, 수컷과 암컷 파리 모두의 안테나에 있는 T1 센실라에 위치한 수십 개의 후각 뉴런을 활성화합니다. 11-cis Vaccenyl Acetate  Chemical Structure
  8. GC40394 11-deoxy Corticosterone

    11-디옥시 코르티코스테론은 부신에서 생성되는 스테로이드 호르몬으로, 미네랄코르티코이드 활성을 가지며 알도스테론 전구체로 작용합니다.

    11-deoxy Corticosterone  Chemical Structure
  9. GC10821 11-keto-β-Boswellic Acid 11-Keto-beta-boswellic acid(11-Keto-β-boswellic acid)는 인도 유향으로 널리 알려진 Boswellia serrate tree의 껍질에서 추출한 올레오검 수지의 5환형 트리테르펜산입니다. 11-Keto-beta-boswellic acid는 주로 5-lipoxygenase(5-LOX) 및 후속 류코트리엔 및 핵 인자-카파 B(NF-κB) 활성화 및 종양 괴사 인자 알파 생성을 억제하기 때문에 항염증 활성이 있습니다. 생산. 11-keto-β-Boswellic Acid  Chemical Structure
  10. GC61538 11-Oxo etiocholanolone 11-Oxo etiocholanolone (11-Ketoetiocholanolone)은 Etiocholanolone의 대사 산물입니다. 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 11-trans 류코트리엔 E4는 류코트리엔 E4(LTE4)의 이성질체입니다. 11-trans Leukotriene E4  Chemical Structure
  14. GC63796 116-9e 116-9e(MAL2-11B)는 Hsp70 공동 샤페론 DNAJA1 억제제입니다. 116-9e  Chemical Structure
  15. GC34016 11beta-Hydroxyprogesterone (11β-Hydroxyprogesterone) 11베타-하이드록시프로게스테론(11&베타;-하이드록시프로게스테론)은 11β의 강력한 억제제입니다. 또한 ED50이 10nM인 COS-7 세포에서 인간 미네랄 코르티코이드 수용체를 활성화합니다. 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 12-하이드록시라우르산은 내인성 대사산물입니다. 12-hydroxy Lauric Acid  Chemical Structure
  24. GC60443 12-Ketodeoxycholic acid 12-케토데옥시콜산은 담즙산으로 신장에서 대사산물입니다. 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 리놀레산의 15-리폭시게나제(15-LOX) 대사 산물인 13(S)-HODE(13(S)-HODE)는 PPARγ을 활성화하는 내인성 리간드로 기능합니다. 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 13-시스-비타민 A 팔미테이트(13-시스-레티닐 팔미테이트)는 콘플레이크의 비타민 A 팔미테이트에 의해 형성된 13-시스 이성질체입니다. 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 14(S)-HDHA(14(S)-HDoHE)는 도코사헥사엔산(DHA)의 산소화 생성물입니다. 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 ASM(acetoxyscirpenol moiety mycotoxins) 중 하나인 15-acetoxyscirpenol은 caspase-3와 무관한 다른 caspase를 활성화하여 용량 의존적으로 Jurkat T 세포 성장을 억제하고 세포 사멸을 강력하게 유도합니다. 15-acetoxy Scirpenol  Chemical Structure
  59. GC19442 15-Acetyldeoxy Nivalenol 15-Acetyldeoxy Nivalenol은 곡물에서 발견되는 고독성 트리코테센이며, deoxynivalenol의 대사산물로 HepG2 세포에 독성을 나타냅니다. 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 15-리폭시게나제 억제제 1은 IC50이 18 μ인 15-리폭시게나제의 선택적 억제제입니다. 15-리폭시게나제 억제제 1은 IC50이 각각 19.5 μM 및 19.1 μM입니다. 대두 15-리폭시게나제(SLO) 및 인간 15-리폭시게나제-1(15)-LOX-1(15)- 15-Lipoxygenase Inhibitor 1은 전립선암 연구에 잠재력이 있습니다. 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-하이드록시 프레드니솔론은 시토크롬 P450 3A(CYP3A) 효소를 통한 글루코코르티코이드 부데소나이드의 22(R) 에피머의 입체 선택적 대사 산물입니다. 16α-hydroxy Prednisolone  Chemical Structure
  65. GC35058 16-Dehydroprogesterone 16-디하이드로프로게스테론은 스테로이드성 프로게스틴입니다. 16-Dehydroprogesterone  Chemical Structure
  66. GC46451 16F16 A PDI inhibitor 16F16  Chemical Structure
  67. GC45909 17α-hydroxy Pregnenolone 1&7#945;-하이드록시 프레그네놀론은 프레그난 스테로이드입니다. 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)는 62 ±의 EC50으로 Hsp90에 결합하는 Hsp90의 강력한 억제제입니다. 29nM. 17-DMAG  Chemical Structure
  78. GC13044 17-DMAG (Alvespimycin) HCl 17-DMAG(알베스피마이신) HCl(17-DMAG 염산염; KOS-1022; BMS 826476)은 62&7#177;29nM의 EC50으로 Hsp90에 결합하는 Hsp90의 강력한 억제제입니다. 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-식이유래 화합물인 글리시레틴산은 다세포 유기체에서 장수 및 항응집 인자로 작용하는 NF-kB의 억제제이자 프로테아좀의 활성화제입니다. 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 18-히드록시코르티코스테론은 코르티코스테로이드이자 코르티코스테론의 유도체로 심각한 전해질 불균형을 유발할 수 있습니다. 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 1G244는 IC50이 각각 12nM 및 84nM인 강력한 DPP8/9 억제제입니다. 1G244는 DPPIV 및 DPPII를 억제하지 않습니다. 1G244는 다발성 골수종 세포에서 세포 사멸을 유도하고 항골수종 효과가 있습니다. 1G244  Chemical Structure
  87. GC38359 1H-pyrazole 1H-피라졸은 내인성 대사 산물입니다. 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;-데옥시아데노신 5′-핵산 AMP 유도체인 모노포스페이트 이나트륨은 DNA에서 발견되는 데옥시리보뉴클레오티드입니다. 2′-Deoxyadenosine 5′-monophosphate disodium  Chemical Structure
  90. GC62772 2’-Deoxyadenosine-5’-triphosphate trisodium &2rsquo;-Deoxyadenosine-5’-triphosphate trisodium(dATP trisodium)은 DNA 중합효소의 기질로서 DNA 합성(또는 복제)을 위해 세포에서 사용되는 뉴클레오티드입니다. 2’-Deoxyadenosine-5’-triphosphate trisodium  Chemical Structure
  91. GC62774 2’-Deoxyguanosine 5’-monophosphate disodium &2rsquo;-데옥시구아노신 5’-일인산 이나트륨(5'-dGMP 이나트륨)은 핵염기로 구아닌을 갖는 모노뉴클레오티드입니다. 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 2',4'-디히드록시아세토페논(Resacetophenone)은 2' 및 4' 위치에 히드록시 치환기를 갖는 아세토페논입니다. 2',4'-Dihydroxyacetophenone  Chemical Structure
  94. GC60462 2',4'-Dimethylacetophenone 2',4'-Dimethylacetophenone  Chemical Structure
  95. GC33605 2'-Deoxyadenosine monohydrate 2'-데옥시아데노신 일수화물은 데옥시리보뉴클레오사이드입니다. 2'-Deoxyadenosine monohydrate  Chemical Structure
  96. GC38258 2'-Deoxyadenosine-5'-monophosphate 핵산 AMP 유도체인 2'-데옥시아데노신 5'-모노포스페이트는 DNA에서 발견되는 데옥시리보뉴클레오티드입니다. 2'-Deoxyadenosine-5'-monophosphate  Chemical Structure
  97. GC42150 2'-Deoxycytidine 5'-diphosphate (sodium salt hydrate) 2'-데옥시시티딘-5'-이인산(dCDP) 삼나트륨은 내인성 대사산물입니다. 2'-Deoxycytidine 5'-diphosphate (sodium salt hydrate)  Chemical Structure
  98. GC17436 2'-Deoxycytidine-5'-monophosphoric acid 2'-Deoxycytidine-5'-monophosphoric acid는 내인성 대사 산물입니다. 2'-Deoxycytidine-5'-monophosphoric acid  Chemical Structure
  99. GC48440 2'-Deoxycytidine-5'-triphosphate (sodium salt) 2'-Deoxycytidine-5'-triphosphate (sodium salt) (dCTP trisodium salt)는 DNA 합성에 사용될 수 있는 뉴클레오시드 삼인산입니다. 2'-Deoxycytidine-5'-triphosphate (sodium salt)  Chemical Structure
  100. GC10897 2'-Deoxyguanosine 2'-Deoxyguanosine(Deoxyguanosine)은 N9 질소에 의해 deoxyribose의 C1 탄소에 연결된 퓨린 뉴클레오사이드 구아닌으로 구성됩니다. 2'-Deoxyguanosine  Chemical Structure
  101. GC38191 2'-Deoxyguanosine monohydrate 2'-Deoxyguanosine monohydrate는 내인성 대사 산물입니다. 2'-Deoxyguanosine monohydrate  Chemical Structure

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