>> 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. GC49887 7-(β-Hydroxyethyl)theophylline-d6 An internal standard for the quantification of 7-(β-hydroxyethyl)theophylline 7-(β-Hydroxyethyl)theophylline-d6  Chemical Structure
  3. GC45707 7-Azido-4-methylcoumarin A fluorescent H2S probe 7-Azido-4-methylcoumarin  Chemical Structure
  4. GC40978 7-epi Maresin 1 7-epi Maresin 1 is the inactive 7(S) epimer of Maresin 1, which contains a 7(R) hydroxyl group. 7-epi Maresin 1  Chemical Structure
  5. GC49312 7-Fluoro-2,1,3-benzoxadiazole-4-sulfonate (ammonium salt) 7-Fluoro-2,1,3-benzoxadiazole-4-sulfonate(암모늄염)는 형광 표지입니다. 7-Fluoro-2,1,3-benzoxadiazole-4-sulfonate (ammonium salt)  Chemical Structure
  6. GC49051 7-hydroxy Methotrexate 7-하이드록시 메토트렉세이트는 메토트렉세이트의 주요 대사 산물입니다. 7-hydroxy Methotrexate  Chemical Structure
  7. GC42608 7-hydroxy Methotrexate (sodium salt)

    7-hydroxy Methotrexate (7-hydroxy MTX) is a phase I metabolite of MTX, which is converted by hepatic aldehyde oxidases.

    7-hydroxy Methotrexate (sodium salt)  Chemical Structure
  8. GC46241 7-keto Cholesterol-d7

    7-keto Cholesterol is a bioactive sterol and a major oxysterol component of oxidized LDL

    7-keto Cholesterol-d7  Chemical Structure
  9. GC48880 7-Methoxyflavone 7-Methoxyflavone은 Zornia brasiliensis에서 분리된 화합물입니다. 7-Methoxyflavone  Chemical Structure
  10. GC13982 7-NINA non-selective NOS inhibitor 7-NINA  Chemical Structure
  11. GC12309 7-Nitroindazole 7-Nitroindazole은 항통각 및 심혈관 효과가 있는 선택적 nNOS 억제제입니다. 7-Nitroindazole  Chemical Structure
  12. GC42616 7-oxo Staurosporine

    7-oxo Staurosporine is an antibiotic originally isolated from S.

    7-oxo Staurosporine  Chemical Structure
  13. GC52211 7-[1-(1H)-Tetrazolylacetamido]desacetoxycephalosporanic Acid A potential impurity in commercial preparations of cefazolin 7-[1-(1H)-Tetrazolylacetamido]desacetoxycephalosporanic Acid  Chemical Structure
  14. GC41136 8(S),15(S)-DiHETE 8(S),15(S)-DiHETE is formed when 15(S)-HETE is subjected to further oxidation by 15-LO. 8(S),15(S)-DiHETE  Chemical Structure
  15. GC42623 8-Bromoguanosine 8-Bromoguanosine is a brominated derivative of guanosine. 8-Bromoguanosine  Chemical Structure
  16. GC35199 8-Deoxygartanin 8-Deoxygartanin, G. 8-Deoxygartanin  Chemical Structure
  17. GC42627 8-Hydroxyguanine (hydrochloride) 8-Hydroxyguanine is produced by oxidative degradation of DNA by hydroxyl radical. 8-Hydroxyguanine (hydrochloride)  Chemical Structure
  18. GC18426 8-Nitroguanine 8-Nitroguanine is a nitrative guanine derivative formed by oxidative damage to the guanine base in DNA by reactive nitrogen species (RNS) during inflammation and in vitro by reaction of DNA with peroxynitrite and other RNS reagents. 8-Nitroguanine  Chemical Structure
  19. GN10212 8-O-Acetyl shanzhiside methyl ester 8-O-Acetyl shanzhiside methyl ester  Chemical Structure
  20. GC49275 8-Oxycoptisine 8-옥시콥티신은 항암 활성이 있는 천연 프로토베르베린 알칼로이드입니다. 8-Oxycoptisine  Chemical Structure
  21. GC46748 9(E),11(E)-12-nitro Conjugated Linoleic Acid A nitrated fatty acid 9(E),11(E)-12-nitro Conjugated Linoleic Acid  Chemical Structure
  22. GC46749 9(E),11(E)-9-nitro Conjugated Linoleic Acid A nitrated fatty acid 9(E),11(E)-9-nitro Conjugated Linoleic Acid  Chemical Structure
  23. GC42633 9(E)-Erythromycin A oxime (9E)-Erythromycin A oxime is a metabolite of the semisynthetic antibiotic roxithromycin . 9(E)-Erythromycin A oxime  Chemical Structure
  24. GC46753 9(S),12(S),13(S)-TriHOME An oxylipin 9(S),12(S),13(S)-TriHOME  Chemical Structure
  25. GC40324 9(S)-PAHSA 9-PAHSA is a newly identified endogenous lipid that belongs to a collection of branched fatty acid esters of hydroxy fatty acids (FAHFAs). 9(S)-PAHSA  Chemical Structure
  26. GC46757 9(Z),11(E)-Conjugated Linoleic Acid (sodium salt) An isomer of linoleic acid 9(Z),11(E)-Conjugated Linoleic Acid (sodium salt)  Chemical Structure
  27. GC42642 9,10-Anthracenediyl-bis(methylene)dimalonic Acid 9,10-안트라센디일-비스(메틸렌)디말론산(ABMDMA)은 단일항 산소 생성(SOG)을 감지하는 데 사용되는 생물학적 염료 및 지시약입니다. 9,10-안트라센디일-비스(메틸렌)디말론산은 안트라센의 수용성 유도체입니다. 9,10-안트라센디일-비스(메틸렌)디말론산은 일중항 산소에 의해 해당 엔도퍼옥사이드로 광표백될 수 있습니다. 이 반응은 400 nm에서 흡광도 감소를 기록하여 분광광도계로 모니터링할 수 있습니다. 9,10-Anthracenediyl-bis(methylene)dimalonic Acid  Chemical Structure
  28. GC42644 9-Deazaguanine 9-Deazaguanine is an analog of guanine that acts as an inhibitor of purine nucleoside phosphorylase (PNP; Kd = 160 nM). 9-Deazaguanine  Chemical Structure
  29. GC42648 9-Methylstreptimidone 9-Methylstreptimidone is a microbial metabolite originally isolated from Streptomyces sp. 9-Methylstreptimidone  Chemical Structure
  30. GC42649 9-Nitrooleate Nitrated unsaturated fatty acids, such as 10- and 12-nitrolinoleate, cholesteryl nitrolinoleate, and nitrohydroxylinoleate, represent a new class of endogenous lipid-derived signalling molecules. 9-Nitrooleate  Chemical Structure
  31. GC42653 9-OxoOTrE 9-OxoOTrE is produced by the oxidation of 9-HpOTrE. 9-OxoOTrE  Chemical Structure
  32. GC40325 9-PAHSA Branched fatty acid esters of hydroxy fatty acids (FAHFAs) are newly identified endogenous lipids regulated by fasting and high-fat feeding and associated with insulin sensitivity. 9-PAHSA  Chemical Structure
  33. GC49237 93-O17O A cationic lipidoid 93-O17O  Chemical Structure
  34. GC49238 93-O17S A cationic lipidoid 93-O17S  Chemical Structure
  35. GC45960 9c(i472) 9c(i472)는 IC50 값이 0.19 μ인 15-LOX-1(15-리폭시게나제-1)의 강력한 억제제입니다. 9c(i472)  Chemical Structure
  36. GC45930 A 26771B A macrolide antibiotic A 26771B  Chemical Structure
  37. GC42660 A-39183A A-39183A is an active component of the A-39183 antibiotic complex produced by aerobic fermentation of Streptomyces NRRL 12049. A-39183A  Chemical Structure
  38. GC42661 A-54556B A-54556B is a natural acyldepsipeptide (ADEP) antibiotic isolated from the fermentation broth of S. A-54556B  Chemical Structure
  39. GC18936 A-83016F A-83016F is an aurodox antibiotic isolated from the actinomycete species A83016. A-83016F  Chemical Structure
  40. GC49309 A-943931 (hydrochloride hydrate) A histamine H4 receptor antagonist A-943931 (hydrochloride hydrate)  Chemical Structure
  41. GC35214 A-9758 A-9758은 RORγ 리간드이자 강력한 선택적 RORγt 역작용제(IC50=5nM)이며 IL-17A 방출에 대한 강력한 효능을 나타냅니다. A-9758  Chemical Structure
  42. GP10060 a-MSH, amide

    a-MSH (α-멜라노사이트 자극 호르몬), 아미드는 멜라노코르틴-1 수용체에 결합하여 G 단백질 운반체를 통해 순환 AMP (cAMP) 신호를 활성화시키고 멜라닌을 합성할 수 있습니다.

    a-MSH, amide  Chemical Structure
  43. GC19496 AAPH

    AAPH is a water-soluble azo compound

    AAPH  Chemical Structure
  44. GC42666 AAT-008 AAT-008은 재조합 인간 EP4 및 재조합 쥐 EP4에 대해 각각 0.97 및 6.1nM의 Kis를 갖는 강력하고 선택적이며 경구 활성인 프로스타글란딘 EP4 수용체 길항제입니다. AAT-008  Chemical Structure
  45. GC65293 AB-680 AB-680은 CD73(외부 뉴클레오티다제)의 매우 강력하고 가역적이며 선택적인 억제제이며, hCD73에 대한 Ki가 4.9pM이고 관련 외부 뉴클레오티다제 CD39에 비해 10,000배 이상의 선택성을 나타냅니다. 항종양 활성. AB-680  Chemical Structure
  46. GC42667 Abacavir Carboxylate Abacavir carboxylate is an inactive metabolite of the HIV-1 reverse transcriptase inhibitor abacavir. Abacavir Carboxylate  Chemical Structure
  47. GC46767 Abacavir-d4 An internal standard for the quantification of abacavir Abacavir-d4  Chemical Structure
  48. GC49766 Abafungin 항진균제인 아바펀진은 스테롤-C-24-메틸트랜스퍼라제 효소에 의해 촉매되는 스테롤 측쇄의 C-24 위치에서 트랜스메틸화를 억제합니다. Abafungin  Chemical Structure
  49. GC42668 ABC34 ABC34 is an inactive control probe for JJH260, the inhibitor of androgen-induced gene 1 (AIG1), an enzyme that hydrolyzes fatty acid esters of hydroxy fatty acids (FAHFAs). ABC34  Chemical Structure
  50. GC49745 ABT-263-d8 ABT-263-d8은 Navitoclax라고 표시된 중수소입니다. Navitoclax(ABT-263)는 Bcl-xL, Bcl-2 및 Bcl-w와 같은 여러 항-세포자멸사 Bcl-2 계열 단백질에 결합하는 강력하고 경구 활성인 Bcl-2 계열 단백질 억제제입니다. 1nM 이상. ABT-263-d8  Chemical Structure
  51. GC42683 Abz-Ala-Pro-Glu-Glu-Ile-Met-Arg-Arg-Gln-EDDnp Abz-Ala-Pro-Glu-Glu-Ile-Met-Arg-Arg-Gln-EDDnp is a fluorescence-quenched peptide substrate for human neutrophil elastase (kcat/Km = 531 mM-1s-1). Abz-Ala-Pro-Glu-Glu-Ile-Met-Arg-Arg-Gln-EDDnp  Chemical Structure
  52. GC52499 Abz-Ala-Pro-Glu-Glu-Ile-Met-Arg-Arg-Gln-EDDnp (trifluoroacetate salt) A sensitive substrate for neutrophil elastase Abz-Ala-Pro-Glu-Glu-Ile-Met-Arg-Arg-Gln-EDDnp (trifluoroacetate salt)  Chemical Structure
  53. GC42684 Abz-Val-Ala-Asp-Nva-Arg-Asp-Arg-Gln-EDDnp (trifluoroacetate salt) Abz-Val-Ala-Asp-Nva-Arg-Asp-Arg-Gln-EDDnp is a fluorescence-quenched peptide substrate for human proteinase 3 (kcat/Km = 1,570 mM-1s-1). Abz-Val-Ala-Asp-Nva-Arg-Asp-Arg-Gln-EDDnp (trifluoroacetate salt)  Chemical Structure
  54. GC42685 Ac-ANW-AMC Ac-ANW-AMC는 면역프로테아좀에 대한 형광 기질입니다. Ac-ANW-AMC  Chemical Structure
  55. GC49704 Ac-FLTD-CMK (trifluoroacetate salt) An inhibitor of caspase-1, -4, -5, and -11 Ac-FLTD-CMK (trifluoroacetate salt)  Chemical Structure
  56. GA20621 Ac-muramic acid

    세균 세포벽의 구성 요소입니다. MurNAc의 보호 된 유도체는 Q-1005를 참조하십시오.

    Ac-muramic acid  Chemical Structure
  57. GC52372 Ac-VDVAD-AFC (trifluoroacetate salt) A fluorogenic substrate for caspase-2 Ac-VDVAD-AFC (trifluoroacetate salt)  Chemical Structure
  58. GC15598 Ac2-26 annexin A1(AnxA1)의 활성 N-말단 펩타이드인 Ac2-26은 허혈 재관류 유발 급성 폐 손상을 약화시킵니다. Ac2-26  Chemical Structure
  59. GC49263 Ac2-26 (human) (ammonium salt) An annexin A1-mimetic peptide Ac2-26 (human) (ammonium salt)  Chemical Structure
  60. GC35224 Ac2-26 TFA 아넥신 A1(AnxA1)의 활성 N-말단 펩타이드인 Ac2-26 TFA는 허혈 재관류 유발 급성 폐 손상을 약화시킵니다. Ac2-26 TFA  Chemical Structure
  61. GC42691 Aceclofenac ethyl ester A potential impurity found in commercial preparations of aceclofenac Aceclofenac ethyl ester  Chemical Structure
  62. GC42692 Aceclofenac methyl ester A potential impurity in commercial preparations of aceclofenac Aceclofenac methyl ester  Chemical Structure
  63. GC49911 Acetyl Hexapeptide-38 (trifluoroacetate salt) A hexapeptide Acetyl Hexapeptide-38 (trifluoroacetate salt)  Chemical Structure
  64. GC42700 Acetyl Pentapeptide-1 Acetyl pentapeptide-1 is a pentapeptide that decreases IL-8 secretion in human keratinocytes when used in combination with acetyl hexapeptide-36 and acetyl hexapeptide-38. Acetyl Pentapeptide-1  Chemical Structure
  65. GC18443 Acetyl-6-formylpterin Acetyl-6-formylpterin is an inhibitor of mucosal-associated invariant T (MAIT) cell activation. Acetyl-6-formylpterin  Chemical Structure
  66. GC11786 Acetylcysteine

    아세틸시스테인은 시스테인의 N-아세틸 유도체입니다.

    Acetylcysteine  Chemical Structure
  67. GC17416 ACHP IκB kinase inhibitor ACHP  Chemical Structure
  68. GN10536 Aconine Aconine  Chemical Structure
  69. GC49804 Acridine An azaarene Acridine  Chemical Structure
  70. GC40645 Actarit 경구 활성 항류마티스 화합물인 Actarit는 II형 콜라겐 유발 관절염을 치료할 가능성이 있습니다. Actarit  Chemical Structure
  71. GC41316 Actinopyrone A Actinopyrone A is a pyrone isolated from S. Actinopyrone A  Chemical Structure
  72. GC48842 Actiphenol A bacterial metabolite with antiviral activity Actiphenol  Chemical Structure
  73. GC46797 Acyclovir-d4 An internal standard for the quantification of acyclovir Acyclovir-d4  Chemical Structure
  74. GC46798 Adapalene-d3 An internal standard for the quantification of adapalene Adapalene-d3  Chemical Structure
  75. GC46805 Adefovir-d4 An internal standard for the quantification of adefovir Adefovir-d4  Chemical Structure
  76. GC31693 Adelmidrol Adelmidrol은 부분적으로 PPARγ에 의존하는 중요한 항염증 효과를 발휘합니다. Adelmidrol  Chemical Structure
  77. GC49285 Adenosine 5’-methylenediphosphate (hydrate) An inhibitor of ecto-5’-nucleotidase Adenosine 5’-methylenediphosphate (hydrate)  Chemical Structure
  78. GC60040 ADH-503 ADH-503((Z)-Leukadherin-1 콜린)은 경구 활성 및 알로스테릭 CD11b 작용제입니다. ADH-503은 종양 관련 대식세포의 재분극을 유도하고, 종양 침윤성 면역억제 골수 세포의 수를 감소시키며, 수지상 세포 반응을 향상시킵니다. ADH-503  Chemical Structure
  79. GC42742 ADT-OH ADT-OH는 황화수소 방출 공여체입니다. ADT-OH는 FADD를 상향 조절하여 세포 사멸을 유도하고 생체 내에서 흑색종의 발달을 억제합니다. ADT-OH는 암 질환 연구의 잠재력을 가지고 있습니다. ADT-OH  Chemical Structure
  80. GC31649 ADU-S100 (ML RR-S2 CDA) ADU-S100(ML RR-S2 CDA)(MIW815), 인터페론 유전자 자극제(STING)의 활성제는 강력하고 전신적인 종양 퇴행 및 면역을 유도합니다. ADU-S100 (ML RR-S2 CDA)  Chemical Structure
  81. GC39161 ADU-S100 disodium salt ADU-S100 이나트륨 염(MIW815 이나트륨 염)은 인터페론 유전자(STING) 자극제의 활성제입니다. ADU-S100 disodium salt  Chemical Structure
  82. GC42743 AEM1 AEM1은 Nrf2 억제제입니다. AEM1은 A549 세포에서 Nrf2 의존성 유전자의 발현을 감소시키고 시험관 내 및 생체 내에서 A549 세포의 성장을 억제합니다. AEM1  Chemical Structure
  83. GC63485 Afimetoran Afimetoran은 염증 및 자가면역 질환 연구에 사용할 수 있는 톨 유사 수용체 길항제입니다. Afimetoran  Chemical Structure
  84. GC66396 Agatolimod 클래스 B ODN(oligodeoxynucleotide)인 Agatolimod(ODN 2006)는 TLR9 작용제입니다. 821d96072c2d58d8970e76f526b0f6b8아가톨리모드는 또한 인간을 위한 최적의 CpG 서열이다. 821d96072c2d58d8970e76f526b0f6b8아가톨리모드는 HD11 세포에서 매우 강력한 NO2 및 IL-6 생성을 자극합니다. 821d96072c2d58d8970e76f526b0f6b8아가톨리모드는 유방암 연구에 사용될 수 있습니다. 821d96072c2d58d8970e76f526b0f6b8시퀀스: 5'-tcgtcgttttgtcgttttgtcgtt-3'.821d96072c2d58d8970e76f526b0f6b8 Agatolimod  Chemical Structure
  85. GC16831 Agmatine sulfate Agmatine sulfate는 신경 전달 물질 시스템, 이온 채널 및 산화 질소 합성과 같은 여러 분자 표적에서 조절 작용을 발휘합니다. Agmatine sulfate  Chemical Structure
  86. GC35271 AHR antagonist 1 AHR 길항제 1(AHR 길항제 1)은 아릴 탄화수소 수용체(AHR) 길항제입니다. AHR antagonist 1  Chemical Structure
  87. GC39669 AHR antagonist 2 AHR 길항제 2는 인간 및 마우스 AhR에 대해 IC50이 0.885 및 2.03nM인 특허 WO2019101641A1, 화합물 실시예 1에서 추출된 강력한 아릴 탄화수소 수용체(AHR) 길항제입니다. AHR antagonist 2  Chemical Structure
  88. GC64275 AHR antagonist 5 특허 WO2018195397, 실시예 39에서 추출된 강력한 경구 활성 아릴 탄화수소 수용체(AHR) 길항제인 AHR 길항제 5는 IC50이 0.5μM 미만입니다. AHR 길항제 5는 체크포인트 억제제 항PD-1과 조합하여 종양 성장을 유의하게 억제합니다. AHR antagonist 5  Chemical Structure
  89. GC64208 AHR antagonist 5 free base AHR 길항제 5 유리 염기는 선택적 경구 활성 아릴 탄화수소 수용체(AHR) 억제제입니다. AHR 길항제 5 유리 염기는 AHR이 세포질에서 핵으로 이동하는 것을 효과적으로 차단합니다. AHR 길항제 5 유리 염기는 다른 수용체, 수송체 및 키나제보다 AHR에 대해 매우 선택적입니다. AHR antagonist 5 free base  Chemical Structure
  90. GC16120 AI-3 Nrf2/Keap1 and Keap1/Cul3 interaction inhibitor AI-3  Chemical Structure
  91. GC46821 Ajoene 마늘에서 추출한 화합물인 아조엔은 항혈전 및 항진균제입니다. Ajoene  Chemical Structure
  92. GC45681 AKP-11 An S1P1 receptor agonist AKP-11  Chemical Structure
  93. GC42763 Alamethicin F50 Alamethicin F50 is a peptaibol isolated from Trichoderma. Alamethicin F50  Chemical Structure
  94. GC49773 Albendazole sulfone-d3 An internal standard for the quantification of albendazole sulfone Albendazole sulfone-d3  Chemical Structure
  95. GC48848 Albendazole-d7 Albendazole-d7(SKF-62979-d7)은 Albendazole로 표시된 중수소입니다. Albendazole-d7  Chemical Structure
  96. GC41080 Albofungin Albofungin is a xanthone isolated from A. Albofungin  Chemical Structure
  97. GC42764 Albuterol methyl ether Salbutamol (albuterol) is a selective β2-adrenergic partial agonist that is used as a bronchodilator. Albuterol methyl ether  Chemical Structure
  98. GC46826 Alclofenac An NSAID Alclofenac  Chemical Structure
  99. GC40638 Alclometasone Dipropionate 알클로메타손 디프로피오네이트(Sch 22219)는 스테로이드 화합물입니다. Alclometasone Dipropionate  Chemical Structure
  100. GN10298 Alibiflorin Alibiflorin  Chemical Structure
  101. GC42769 all-trans Retinoyl β-D-Glucuronide all-trans Retinoyl β-D-glucuronide is a metabolite of all-trans retinoic acid formed by the UDP-glucuronosyltransferase (UGT) system. all-trans Retinoyl β-D-Glucuronide  Chemical Structure

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