>> Signaling Pathways >> Immunology/Inflammation

Immunology/Inflammation

The immune and inflammation-related pathway including the Toll-like receptors pathway, the B cell receptor signaling pathway, the T cell receptor signaling pathway, etc.

Toll-like receptors (TLRs) play a central role in host cell recognition and responses to microbial pathogens. TLR4 initially recruits TIRAP and MyD88. MyD88 then recruits IRAKs, TRAF6, and the TAK1 complex, leading to early-stage activation of NF-κB and MAP kinases [1]. TLR4 is endocytosed and delivered to intracellular vesicles and forms a complex with TRAM and TRIF, which then recruits TRAF3 and the protein kinases TBK1 and IKKi. TBK1 and IKKi catalyze the phosphorylation of IRF3, leading to the expression of type I IFN [2].

BCR signaling is initiated through ligation of mIg under conditions that induce phosphorylation of the ITAMs in CD79, leading to the activation of Syk. Once Syk is activated, the BCR signal is transmitted via a series of proteins associated with the adaptor protein B-cell linker (Blnk, SLP-65). Blnk binds CD79a via non-ITAM tyrosines and is phosphorylated by Syk. Phospho-Blnk acts as a scaffold for the assembly of the other components, including Bruton’s tyrosine kinase (Btk), Vav 1, and phospholipase C-gamma 2 (PLCγ2) [3]. Following the assembly of the BCR-signalosome, GRB2 binds and activates the Ras-guanine exchange factor SOS, which in turn activates the small GTPase RAS. The original RAS signal is transmitted and amplified through the mitogen-activated protein kinase (MAPK) pathway, which including the serine/threonine-specific protein kinase RAF followed by MEK and extracellular signal related kinases ERK 1 and 2 [4]. After stimulation of BCR, CD19 is phosphorylated by Lyn. Phosphorylated CD19 activates PI3K by binding to the p85 subunit of PI3K and produce phosphatidylinositol-3,4,5-trisphosphate (PIP3) from PIP2, and PIP3 transmits signals downstream [5].

Central process of T cells responding to specific antigens is the binding of the T-cell receptor (TCR) to specific peptides bound to the major histocompatibility complex which expressed on antigen-presenting cells (APCs). Once TCR connected with its ligand, the ζ-chain–associated protein kinase 70 molecules (Zap-70) are recruited to the TCR-CD3 site and activated, resulting in an initiation of several signaling cascades. Once stimulation, Zap-70 forms complexes with several molecules including SLP-76; and a sequential protein kinase cascade is initiated, consisting of MAP kinase kinase kinase (MAP3K), MAP kinase kinase (MAPKK), and MAP kinase (MAPK) [6]. Two MAPK kinases, MKK4 and MKK7, have been reported to be the primary activators of JNK. MKK3, MKK4, and MKK6 are activators of P38 MAP kinase [7]. MAP kinase pathways are major pathways induced by TCR stimulation, and they play a key role in T-cell responses.

Phosphoinositide 3-kinase (PI3K) binds to the cytosolic domain of CD28, leading to conversion of PIP2 to PIP3, activation of PKB (Akt) and phosphoinositide-dependent kinase 1 (PDK1), and subsequent signaling transduction [8].

 

References

[1] Kawai T, Akira S. The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors[J]. Nature immunology, 2010, 11(5): 373-384.

[2] Kawai T, Akira S. Toll-like receptors and their crosstalk with other innate receptors in infection and immunity[J]. Immunity, 2011, 34(5): 637-650.

[3] Packard T A, Cambier J C. B lymphocyte antigen receptor signaling: initiation, amplification, and regulation[J]. F1000Prime Rep, 2013, 5(40.10): 12703.

[4] Zhong Y, Byrd J C, Dubovsky J A. The B-cell receptor pathway: a critical component of healthy and malignant immune biology[C]//Seminars in hematology. WB Saunders, 2014, 51(3): 206-218.

[5] Baba Y, Matsumoto M, Kurosaki T. Calcium signaling in B cells: regulation of cytosolic Ca 2+ increase and its sensor molecules, STIM1 and STIM2[J]. Molecular immunology, 2014, 62(2): 339-343.

[6] Adachi K, Davis M M. T-cell receptor ligation induces distinct signaling pathways in naive vs. antigen-experienced T cells[J]. Proceedings of the National Academy of Sciences, 2011, 108(4): 1549-1554.

[7] Rincón M, Flavell R A, Davis R A. The Jnk and P38 MAP kinase signaling pathways in T cell–mediated immune responses[J]. Free Radical Biology and Medicine, 2000, 28(9): 1328-1337.

[8] Bashour K T, Gondarenko A, Chen H, et al. CD28 and CD3 have complementary roles in T-cell traction forces[J]. Proceedings of the National Academy of Sciences, 2014, 111(6): 2241-2246.

Targets for  Immunology/Inflammation

Products for  Immunology/Inflammation

  1. Cat.No. 상품명 정보
  2. GC35412 Asperulosidic Acid Asperulosidic Acid(ASPA)는 생리 활성 이리도이드 배당체이며 Hedyotis diffusa Willd의 허브에서 추출됩니다. Asperulosidic Acid  Chemical Structure
  3. GC42860 Aspochalasin D Aspochalasin D is a co-metabolite originally isolated from A. Aspochalasin D  Chemical Structure
  4. GC46886 Aspyrone A fungal metabolite with diverse biological activities Aspyrone  Chemical Structure
  5. GC31350 Astaxanthin 적색 식이 카로티노이드인 아스타잔틴은 경구로 효과적이고 강력한 항산화제입니다. Astaxanthin  Chemical Structure
  6. GC68702 Astegolimab

    Astegolimab (MSTT 1041A; RG 6149) is a human IgG2 monoclonal antibody that blocks IL-33 signaling by targeting the IL-33 receptor ST2. Astegolimab has potential for use in chronic obstructive pulmonary disease (COPD) research.

    Astegolimab  Chemical Structure
  7. GC41640 Asterriquinol D dimethyl ether Asterriquinol D 디메틸 에테르는 28 μg/mL의 IC50으로 마우스 골수종 NS-1 세포주를 억제할 수 있는 곰팡이 대사 산물입니다. Asterriquinol D dimethyl ether  Chemical Structure
  8. GN10415 Astilbin Astilbin  Chemical Structure
  9. GC42863 Asukamycin Asukamycin is polyketide isolated from the S. Asukamycin  Chemical Structure
  10. GC32457 Asymmetric dimethylarginine 비대칭 디메틸아르기닌은 산화질소 합성효소(NOS)의 내인성 억제제이며 여러 병리학적 상태에서 내피 기능 장애의 표지자로 기능합니다. Asymmetric dimethylarginine  Chemical Structure
  11. GC46091 Aszonapyrone A Aszonapyrone A는 Aspergillus zonatus에 의해 생성되는 대사 산물입니다. Aszonapyrone A  Chemical Structure
  12. GC39554 AT2 receptor agonist C21 AT2 수용체 작용제 C21은 AT2 수용체 및 AT1 수용체에 대해 각각 0.4 nM 및 >10 μM의 Ki 값을 갖는 약물 유사 선택적 안지오텐신 II AT2 수용체 작용제이다. AT2 receptor agonist C21  Chemical Structure
  13. GC62334 AT791 AT791은 강력하고 경구 생체이용 가능한 TLR7 및 TLR9 억제제입니다. AT791  Chemical Structure
  14. GC46887 Atazanavir-d6 An internal standard for the quantification of atazanavir Atazanavir-d6  Chemical Structure
  15. GC12537 ATB-337 ATB-337은 H2S 기증자와 NSAID 디클로페낙의 하이브리드 분자입니다. ATB-337  Chemical Structure
  16. GC16245 ATB-343 hybrid molecule of an H2S donor and the NSAID indomethacin ATB-343  Chemical Structure
  17. GC46892 ATRA-BA Hybrid A prodrug form of all-trans retinoic acid and butyric acid ATRA-BA Hybrid  Chemical Structure
  18. GN10627 Atractylenolide I Atractylenolide I  Chemical Structure
  19. GC48925 Aureonitol A fungal metabolite Aureonitol  Chemical Structure
  20. GC41490 Aureusimine B Aureusimine B, also known as phevalin, is a natural pyrazinone produced by certain fungi and by Staphylococcus spp., including S. Aureusimine B  Chemical Structure
  21. GC46895 Aurintricarboxylic Acid (ammonium salt) A protein synthesis inhibitor with diverse biological activities Aurintricarboxylic Acid (ammonium salt)  Chemical Structure
  22. GC40005 Aurodox

    Aurodox is a polyketide antibiotic originally isolated from S.

    Aurodox  Chemical Structure
  23. GC49646 Aurothioglucose (hydrate) A TrxR inhibitor Aurothioglucose (hydrate)  Chemical Structure
  24. GC42877 AUY954 AUY954 is an orally bioavailable and selective agonist of the sphingosine-1-phosphate receptor 1 (S1P1; EC50 = 1.2 nM for stimulating GTPγS binding to S1P1 in CHO cells). AUY954  Chemical Structure
  25. GC32486 AVE-3085 AVE-3085는 심혈관 질환 치료에 사용되는 강력한 내피 산화질소 합성효소 증강제입니다. AVE-3085  Chemical Structure
  26. GC42880 Avenanthramide-C methyl ester Avenanthramide-C methyl ester is an inhibitor of NF-κB activation that acts by blocking the phosphorylation of IKK and IκB (IC50 ~ 40 μM). Avenanthramide-C methyl ester  Chemical Structure
  27. GC45388 Averantin Averantin은 곰팡이 Cercospora arachidicola의 소량 대사 산물입니다. Averantin  Chemical Structure
  28. GC42881 Avermectin B1a aglycone Avermectin B1a aglycone is an aglycone form of the anthelmintic and insecticide avermectin B1a. Avermectin B1a aglycone  Chemical Structure
  29. GC42882 Avermectin B1a monosaccharide Avermectin B1a monosaccharide is a macrolide anthelmintic and monosaccharide form of avermectin B1a. Avermectin B1a monosaccharide  Chemical Structure
  30. GC45984 Avilamycin A An antibiotic Avilamycin A  Chemical Structure
  31. GC48511 Avrainvillamide Avrainvillamide((+)-Avrainvillamide)는 항증식 효과가 있는 자연 발생 알칼로이드로, 다양한 인간 종양에서 과발현되는 제안된 발암성 단백질인 핵 샤페론 뉴클레오포스민에 결합합니다. Avrainvillamide  Chemical Structure
  32. GC42885 AX 048 The group IVA phospholipase A2 (PLA2), known as calcium-dependent cytosolic PLA2 (cPLA2), selectively releases arachidonic acid from membrane phospholipids, playing a central role in initiating the synthesis of prostaglandins and leukotrienes. AX 048  Chemical Structure
  33. GC35440 AX-024 AX-024는 TCR에 의해 유발되는 T 세포 활성화를 IC50 ~1 nM으로 선택적으로 억제하는 TCR-Nck 상호작용의 경구 사용 가능한 동급 최초의 억제제입니다. AX-024  Chemical Structure
  34. GC19046 AX-024 hydrochloride AX-024 염산염은 IC50 ~1 nM으로 TCR에 의해 유발되는 T 세포 활성화를 선택적으로 억제하는 TCR-Nck 상호작용의 구두로 이용 가능한 동급 최초의 억제제입니다. AX-024 hydrochloride  Chemical Structure
  35. GC65283 AXC-715 trihydrochloride AXC-715(T785) 삼염산염은 특허 WO2020168017 A1에서 추출한 TLR7/TLR8 이중 작용제입니다. AXC-715 trihydrochloride  Chemical Structure
  36. GC64938 AZD-7648 AZD-7648은 IC50이 0.6nM인 강력한 경구 활성 선택적 DNA-PK 억제제입니다. AZD-7648은 세포사멸을 유도하고 항종양 활성을 나타낸다. AZD-7648  Chemical Structure
  37. GC10135 AZD3264 AZD3264는 선택적 IkB 키나제 IKK2 억제제입니다. AZD3264  Chemical Structure
  38. GC62488 AZD8848 AZD8848은 천식 및 알레르기 비염 연구를 위해 개발된 선택적 톨유사 수용체 7(TLR7) 항약물 작용제이다. AZD8848  Chemical Structure
  39. GC49057 Azelastine-13C-d3 (hydrochloride) An internal standard for the quantification of azelastine Azelastine-13C-d3 (hydrochloride)  Chemical Structure
  40. GC42891 azido-FTY720 Azido-FTY720은 FTY720의 광활성화 유사체입니다. azido-FTY720  Chemical Structure
  41. GC46903 Azithromycin-d3 아지트로마이신-d3(CP 62993-d3)은 아지트로마이신으로 표시된 중수소입니다. Azithromycin-d3  Chemical Structure
  42. GC46904 Azoxystrobin 아족시스트로빈은 광범위한 스펙트럼의 β-메톡시아크릴레이트 살균제입니다. Azoxystrobin  Chemical Structure
  43. GC60616 AZT triphosphate AZT 삼인산(3'-Azido-3'-deoxythymidine-5'-triphosphate)은 지도부딘(AZT)의 활성 삼인산 대사 산물입니다. AZT triphosphate  Chemical Structure
  44. GC60617 AZT triphosphate TEA AZT 삼인산 TEA(3'-Azido-3'-deoxythymidine-5'-triphosphate TEA)는 지도부딘(AZT)의 활성 삼인산 대사 산물입니다. AZT triphosphate TEA  Chemical Structure
  45. GC45795 Aztreonam-d6 An internal standard for the quantification of aztreonam Aztreonam-d6  Chemical Structure
  46. GC39280 B022 B022는 강력하고 선택적인 NF-κB 유도 키나제(NIK) 억제제입니다(Ki 4.2nM; IC50=15.1nM). B022  Chemical Structure
  47. GC18580 B355252 페녹시 티오펜 설폰아미드 소분자인 B355252는 강력한 NGF 수용체 작용제입니다. B355252  Chemical Structure
  48. GC42895 Bacillosporin C Bacillosporin C is an oxaphenalenone dimer originally isolated from T. Bacillosporin C  Chemical Structure
  49. GC49793 Bacitracin A (technical grade) A polypeptide antibiotic Bacitracin A (technical grade)  Chemical Structure
  50. GC46905 Bacitracin Complex A mixture of bacitracin polypeptides in complex with copper Bacitracin Complex  Chemical Structure
  51. GC45938 Bacopaside X Bacopaside X는 Bacopa monnieri에서 발견되며 D1 수용체에 대한 결합 친화성을 나타냅니다. Bacopaside X  Chemical Structure
  52. GC49302 Bactenecin (bovine) (trifluoroacetate salt) A cationic peptide Bactenecin (bovine) (trifluoroacetate salt)  Chemical Structure
  53. GN10018 Baicalin

    다양한 생물학적 활동을 가진 플라보노이드

    Baicalin  Chemical Structure
  54. GC52344 Bak BH3 (72-87) (human) (trifluoroacetate salt) A Bak-derived peptide Bak BH3 (72-87) (human) (trifluoroacetate salt)  Chemical Structure
  55. GC18126 Balsalazide Balsalazide는 IL-6/STAT3 경로의 조절을 통해 대장염 관련 발암을 억제할 수 있습니다. Balsalazide  Chemical Structure
  56. GC35466 Balsalazide sodium hydrate Balsalazide sodium hydrate는 IL-6/STAT3 경로의 조절을 통해 대장염 관련 발암을 억제할 수 있습니다. Balsalazide sodium hydrate  Chemical Structure
  57. GC17574 BAPTA BAPTA는 칼슘에 대한 선택적 킬레이트제입니다. BAPTA  Chemical Structure
  58. GC18313 BAR501 Impurity BAR501 impurity is an impurity found in the preparation of BAR501 that acts as an agonist of the G protein-coupled bile acid-activated receptor (GP-BAR1). BAR501 Impurity  Chemical Structure
  59. GC66331 Basiliximab Basiliximab(CHI 621)은 재조합 키메라 쥐/인간 IgG1 단일클론 항인터루킨-2 수용체 항체입니다. 821d96072c2d58d8970e76f526b0f6b8Basiliximab은 신장 이식 연구에 사용할 수 있습니다.821d96072c2d58d8970e76f526b0f6b8 Basiliximab  Chemical Structure
  60. GC52476 Bax Inhibitor Peptide V5 (trifluoroacetate salt) A Bax inhibitor Bax Inhibitor Peptide V5 (trifluoroacetate salt)  Chemical Structure
  61. GC10345 Bay 11-7085 BAY 11-7085(BAY 11-7083)는 NF-κB 활성화 및 IκBα의 인산화 억제제입니다. 10μM의 IC50으로 IκBα를 안정화합니다. Bay 11-7085  Chemical Structure
  62. GC13035 Bay 11-7821

    선택적이고 불가역적인 NF-κB 억제제

    Bay 11-7821  Chemical Structure
  63. GC42897 BAY 61-3606 (hydrochloride) BAY 61-3606 is a cell-permeable, reversible inhibitor of spleen tyrosine kinase (Syk; Ki = 7.5 nM; IC50 = 10 nM). BAY 61-3606 (hydrochloride)  Chemical Structure
  64. GC35474 Bay 65-1942 free base Bay 65-1942 유리 염기는 ATP 경쟁적이고 선택적 IKKβ 억제제입니다. Bay 65-1942 free base  Chemical Structure
  65. GC16303 Bay 65-1942 HCl salt Bay 65-1942 HCl salt  Chemical Structure
  66. GC35475 Bay 65-1942 R form Bay 65-1942 R 형태는 Bay 65-1942의 덜 활동적인 R 형태입니다. Bay 65-1942 R form  Chemical Structure
  67. GC60624 BAY-985 BAY-985는 TBK1(낮은/높은 ATP) 및 IKKε에 대한 IC50이 각각 2/30 및 2nM인 TBK1 및 IKKε의 매우 강력한 경구 활성 및 선택적 ATP 경쟁 이중 억제제입니다. 항종양 효능. BAY-985  Chemical Structure
  68. GC12232 BAY-X 1005 BAY-X 1005(BAY X 1005; DG-031)는 경구 활성 및 선택적 5-리폭시게나제 활성화 단백질(FLAP) 억제제입니다. BAY-X 1005  Chemical Structure
  69. GC18487 BC-1215 BC-1215는 F-box 단백질 3(Fbxo3) 억제제입니다. BC-1215  Chemical Structure
  70. GC41583 BCN-E-BCN BCN-E-BCN is a strained cycloalkyne probe for detecting proteins that have been sulfenylated, the first intermediate step in protein oxidation. BCN-E-BCN  Chemical Structure
  71. GC35481 BCX 1470 BCX 1470은 트립신보다 인자 D(IC50=96nM) 및 C1(IC50=1.6nM)의 에스테르분해 활성을 각각 3.4배 및 200배 더 잘 억제합니다. BCX 1470  Chemical Structure
  72. GC35482 BCX 1470 methanesulfonate BCX 1470 메탄설포네이트는 트립신보다 인자 D(IC50=96nM) 및 C1(IC50=1.6nM)의 에스테르분해 활성을 각각 3.4배 및 200배 더 잘 억제합니다. BCX 1470 methanesulfonate  Chemical Structure
  73. GC46908 BE-24566B A fungal metabolite BE-24566B  Chemical Structure
  74. GC46910 Beauvericin A A cyclodepsipeptide with diverse biological activities Beauvericin A  Chemical Structure
  75. GC49038 Benanomicin A A microbial metabolite with antifungal, fungicidal, and antiviral activities Benanomicin A  Chemical Structure
  76. GC52468 Benanomicin B A microbial metabolite with antifungal, fungicidal, and antiviral activities Benanomicin B  Chemical Structure
  77. GC49040 Benanomicin B (formate) A microbial metabolite with antifungal, fungicidal, and antiviral activities Benanomicin B (formate)  Chemical Structure
  78. GC49042 Benastatin A A bacterial metabolite with diverse biological activities Benastatin A  Chemical Structure
  79. GC49043 Benastatin B A bacterial metabolite with diverse biological activities Benastatin B  Chemical Structure
  80. GC49044 Benastatin C A bacterial metabolite with diverse biological activities Benastatin C  Chemical Structure
  81. GC64354 Bendamustine 퓨린 유사체인 벤다무스틴(SDX-105 유리 염기)은 DNA 가교제입니다. 벤다무스틴은 DNA 손상 스트레스 반응과 세포자멸사를 활성화합니다. 벤다무스틴은 강력한 알킬화, 항암 및 항대사 물질 특성을 가지고 있습니다. Bendamustine  Chemical Structure
  82. GC34046 Bendazol Bendazol은 또한 신장 사구체 및 집합 세뇨관에서 NO 합성 효소 활성을 향상시킬 수 있는 저혈압 약물입니다. Bendazol  Chemical Structure
  83. GC15949 Benfotiamine A lipid-soluble form of vitamin B1 Benfotiamine  Chemical Structure
  84. GC49836 Benoxaprofen 베녹사프로펜(LRCL 3794)은 강력하고 오래 지속되는 항염증 및 해열 화합물입니다. Benoxaprofen  Chemical Structure
  85. GC39346 Benralizumab 벤랄리주맙(MEDI-563)은 인터루킨-5 수용체 α(IL-5Rα)-유도 세포용해 단일클론 항체로, 항체 의존성 세포 매개 세포독성 강화를 통해 호산구의 직접적이고 신속하며 거의 완전한 고갈을 유도합니다. Benralizumab  Chemical Structure
  86. GC35494 Benzoyloxypaeoniflorin Paeonia suffruticosa의 뿌리에서 분리된 Benzoyloxypaeoniflorin은 IC50이 0.453mM인 버섯 티로시나제에 대한 티로시나제 억제제입니다. Benzoyloxypaeoniflorin  Chemical Structure
  87. GC15058 Benzydamine HCl Benzydamine HCl은 국소 마취 및 진통 특성을 지닌 국소 작용 비스테로이드성 항염증제입니다. 프로스타글란딘 합성효소에 선택적으로 결합하고 현저한 시험관내 항균 활성이 있습니다. Benzydamine HCl  Chemical Structure
  88. GC60636 Benzyl butyl phthalate 프탈산 에스테르(PAE)의 구성원인 벤질 부틸 프탈레이트는 Zeb1의 상향 조절을 통해 혈관종(HA) 세포의 이동 및 침입을 유발할 수 있습니다. 벤질 부틸 프탈레이트는 유방암 세포에서 아릴 탄화수소 수용체(AhR)를 활성화하여 SPHK1/S1P/S1PR3 신호 전달을 자극하고 전이 개시 유방암 줄기 세포(BCSC)의 형성을 향상시킵니다. Benzyl butyl phthalate  Chemical Structure
  89. GN10443 Berbamine Berbamine  Chemical Structure
  90. GN10358 Berbamine hydrochloride Berbamine hydrochloride  Chemical Structure
  91. GN10221 Berberine

    베르베린 (자연 황색 18)은 중국의 한약인 황련에서 분리된 알칼로이드로 항생제 역할을 합니다. 베르베린 (자연 황색 18)은 반응성 산소 종 (ROS) 생성을 유도하고 DNA 탑오이소메라아제를 억제합니다.

    Berberine  Chemical Structure
  92. GC35497 Berberine chloride hydrate Berberine chloride hydrate(Natural Yellow 18 chloride hydrate)는 항생물질로 작용하는 알칼로이드입니다. Berberine chloride hydrate는 활성산소(ROS) 생성을 유도하고 DNA topoisomerase를 억제합니다. 항종양 특성. Berberine chloride hydrate  Chemical Structure
  93. GN10208 Berberine hydrochloride

    Berberine hydrochloride is an isoquinoline alkaloid derived from the Ranunculaceae medicinal plant Coptis chinensis. It has various pharmacological activities such as anti-tumor, anti-inflammatory, and hypoglycemic activities.

    Berberine hydrochloride  Chemical Structure
  94. GN10523 Berberine Sulfate Berberine Sulfate  Chemical Structure
  95. GC49387 Berberine-d6 (chloride) An internal standard for the quantification of berberine Berberine-d6 (chloride)  Chemical Structure
  96. GC46098 Berkeleylactone E A macrolide antibiotic Berkeleylactone E  Chemical Structure
  97. GC42925 Berteroin 자연적으로 발생하는 설포라판 유사체인 베르테로인(Berteroin)은 항전이제입니다. Berteroin  Chemical Structure
  98. GC46922 Betamethasone 21-phosphate (sodium salt hydrate) A synthetic glucocorticoid Betamethasone 21-phosphate (sodium salt hydrate)  Chemical Structure
  99. GC52329 Betamethasone-d5 An internal standard for the quantification of betamethasone Betamethasone-d5  Chemical Structure
  100. GC10480 Betulinic acid A plant triterpenoid similar to bile acids Betulinic acid  Chemical Structure
  101. GC48504 Betulinic Aldehyde oxime A derivative of betulin Betulinic Aldehyde oxime  Chemical Structure

Items 601 to 700 of 2909 total

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