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抑制剂 & 化合物

1

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Cat. No.	Product Name	Target	Signaling Pathways
TQ0174	Mavorixafor AMD-070	CXCR	Autophagy; GPCR/G Protein; Immunology/Inflammation
	Mavorixafor (AMD-070) 是一种有效的特异性 CXCR4 拮抗剂，对 CXCR4 125I-SDF 结合的 IC50 值为 13 nM。 Mavorixafor 在 MT-4 细胞 (IC50 = 1 nM) 和 PBMC (IC50 = 9 nM) 中抑制 T-tropic HIV-1 (NL4.3 株) 的复制。
T7208	AMD 3465 hexahydrobromide GENZ-644494 (hexahydrobromide)	HIV Protease; CXCR	Autophagy; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome
	AMD 3465 hexahydrobromide (GENZ-644494 (hexahydrobromide)) 是一种 CXCR4受体拮抗剂，具有潜在的抗癌和抗 HIV 活性。
T22565	AMD-070 hydrochloride N-(1H-苯并咪唑-2-基甲基)-N-[(8S)-5,6,7,8-四氢-8-喹啉基]-1,4-丁二胺单盐酸盐	CXCR	Autophagy; GPCR/G Protein; Immunology/Inflammation
	AMD-070 hydrochloride 是一种 CXCR4 拮抗剂，可用于抗 HIV。
T29957	AMD-7049 AMD 7049
	AMD-7049 is a biochemical.
T1776	Plerixafor 普乐沙福,JM3100,AMD 3100,AMD-3329	Virus Protease; HIV Protease; CXCR	Autophagy; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome
	Plerixafor (AMD-3329) 是一种趋化因子受体拮抗剂，可阻断基质细胞衍生因子与细胞受体 CXCR4 的结合。它也是 CXCR7 的变构激动剂，是免疫刺激剂和造血干细胞动员剂，还抑制HIV-1和HIV-2的复制，EC50为 1-10 nM。
T29958	AMD-9370
	AMD-9370 is a biochemical.
T14208	AMD 3465 GENZ-644494	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	AMD 3465 also potently inhibits the replication of X4 HIV strains (IC50: 1-10 nM). However, it has no effect on CCR5-using (R5) viruses. AMD 3465 (GENZ-644494) is a potent antagonist of CXCR4, inhibits binding of 12G5 mAb and CXCL12AF647 to CXCR4, with IC
T1776L	Plerixafor octahydrochloride 盐酸普乐沙福,JM3100 octahydrochloride,Plerixafor 8HCl (AMD3100 8HCl),Plerixafor 8HCl,SID791 octahydrochloride,AMD 3100 octahydrochloride,JM 3100 8HCl	Virus Protease; HIV Protease; CXCR	Autophagy; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome
	Plerixafor octahydrochloride (JM3100 octahydrochloride) 是一种选择性的CXCR4拮抗剂，IC50为 44 nM。Plerixafor 是一种具有造血干细胞动员活性的双环霉素。
T21323	Picoplatin NX 473,AMD-473,AMD473,NX-473,NX473,AMD 473
	Picoplatin has a broad spectrum of antineoplastic activity and is designed to overcome platinum drug resistance. Picoplatin alkylates DNA, forming both intra- and inter-strand cross-linkages, resulting in the inhibition of DNA replication and transcriptio
T10296	Mavorixafor trihydrochloride AMD-070 trihydrochloride	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	Mavorixafor trihydrochloride is a selective and orally available CXCR4 antagonist (IC50: 13 nM against CXCR4 125I-SDF binding) and also inhibits the replication of T-tropic HIV-1 (NL4.3 strain) in MT-4 cells and PBMCs (IC50s: 1 and 9 nM).
T69583	AMD-3451 trihydrochloride
	AMD-3451 trihydrochloride is a CCR5/CXCR4 dual antagonist that may be useful in the treatment of HIV.
T70260	AMD-3329 hydrobromide
	AMD-3329 hydrobromide is a biochemical in the class of potent and selective anti-HIV-1 and HIV-2 agents that inhibit virus replication by binding to the chemokine receptor CXCR4, the co-receptor for entry of X4 viruses.
T70259	AMD-3329 free base
	AMD-3329 free base is a biochemical in the class of potent and selective anti-HIV-1 and HIV-2 agents that inhibit virus replication by binding to the chemokine receptor CXCR4, the co-receptor for entry of X4 viruses.
T69582	AMD-3451 free base
	AMD-3451 free base is a dual CCR5/CXCR4 antagonist which may be useful in the treatment of a wide variety of R5, R5/X4, and X4 strains of human immunodeficiency virus type 1 (HIV-1) and HIV-2. AMD3451 is the first low-molecular-weight anti-HIV agent with selective HIV coreceptor, CCR5 and CXCR4, interaction.
T8574	SPHINX	Others	Others
	SPHINX 是新一代的 SPRK1抑制剂。
T9928	Ranibizumab	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	Ranibizumab 是一种人源化单克隆抗体片段，旨在靶向和抑制血管内皮生长因子 (VEGF)，包括 VEGF110、VEGF121 和 VEGF165。 Ranibizumab 选择性靶向和中和 VEGF-A 同工型的能力使其成为湿性年龄相关性黄斑变性 (AMD) 研究和治疗策略的重要组成部分。
T23716	AMDE-1 AMDE 1	Autophagy	Autophagy
	AMDE-1 是一种自噬调节剂，以 Atg5 依赖性方式触发自噬。 AMDE-1 将 Atg16 募集到自噬体前位点并导致 LC3 脂化。
T69725	Amdakefalin
	Amdakefalin is a μ and δ opioid receptors agonist that acts as an analgesic.
T39327	Amdizalisib Amdizalisib,HMPL-689
	Amdizalisib is a PI3K inhibitor and used for the research of inflammatory disease, autoimmune disease or cancer.
T26615	Amdoxovir AMDX,DAPD
	Amdoxovir is a reverse transcriptase inhibitor.
T29959	Amdinocillin methylacetate Mecillinam acetylmethyl ester
	Amdinocillin methylacetate is a Synthetic penicillin.
T13157	TG 100801 TG100801,TG 100572	VEGFR; Src	Angiogenesis; Tyrosine Kinase/Adaptors
	TG 100801 是 VEGFr2 和 Src 家族（Src 和 YES）激酶的双重抑制剂，是治疗年龄相关性黄斑变性（AMD）的候选化合物。
T3306	PF-04418948 PF 04418948,PF04418948	Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation
	PF-04418948 是一种可口服的，选择性的前列腺素EP2受体拮抗剂，IC50为16 nM。
T7493	AG-13958 AG-013958,N-[2-氟-5-[[3-[(1E)-2-(2-吡啶基)乙烯基]-1H-吲唑-6-基]氨基]苯基]-1,3-二甲基-1H-吡唑-5-甲酰胺	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	AG-13958 (AG-013958) 是 VEGFR 酪氨酸激酶抑制剂，可用于年龄相关性黄斑变性 (AMD) 的脉络膜新生血管形成的研究。
T69452	AG-13958 monohydrochloride
	AG-13958 monohydrochloride is the HCl salt of AG-13958 --- a VEGFA inhibitor potentially for the treatment of age-related macular degeneration. Neovascular AMD, a subtype characterized by the growth of new, pathologic blood vessels, results in most of the cases of severe and rapid vision loss associated with AMD. A critical activator of angiogenesis in neovascular AMD is VEGF.
T28008	MDVN1003 MDVN 1003,MDVN-1003
	MDVN1003 is a potent inhibitor of BTK amd PI3Kδ, two proteins regulated by the B cell receptor (BCR) that drive the growth of many NHLs. MDVN1003 induces cell death in a B cell lymphoma cell line but not in an irrelevant erythroblast cell line.
T74551	Avacincaptad pegol sodium
	Avacincaptad pegol (ARC1905) 是一种靶向补体因子5 (C5)的核酸适配体，抑制C5剪切为C5a 和C5b。Avacincaptad pegol 被用于研究与年龄相关的黄斑变性(AMD)。
T39706	Pegaptanib sodium
	Pegaptanib sodium, an RNA aptamer specifically targeting vascular endothelial growth factor (VEGF)-165, holds great promise for investigating neovascular age-related macular degeneration (AMD).
TP1390	CEP dipeptide 1
	CEP dipeptide 1, a potent angiogenic compound, exhibits robust activity in promoting angiogenesis. This compound is specifically implicated in the pathogenesis of age-related macular degeneration (AMD).
T77016	Galegenimab
	Galegenimab (FHTR 2163; RG 6147; RO 7171009)，一种抗 HTRA1抗体片段。Galegenimab 可用于年龄相关性黄斑变性 (AMD) 研究。
TP1464	Risuteganib hydrochloride
	Risuteganib hydrochloride is an anti-integrin that downregulates oxidative stress and restores homeostasis, and targets three integrin receptors that are implicated in dry age-related macular degeneration (AMD) in order to restore homeostasis in the retin
T76987	Tarcocimab
	Tarcocimab (OG1953) 是一种人源化抗VEGFA 单克隆抗体 (IgG1 型)。Tarcocimab 可用于视网膜静脉阻塞 (RVO) 和湿性老年性黄斑变性 (AMD) 的研究。
T74552	Non-PEGylated/naked ARC1905
	Non-PEGylated/naked ARC1905 是一种没有偶联PEG 的靶向补体因子5 (C5)的核酸适配体，抑制C5剪切为C5a 和C5b。Non-PEGylated/naked ARC1905 被用于研究与年龄相关的黄斑变性(AMD)。
T75156L	Bevasiranib sodium
	Bevasiranib sodium 是一种siRNA，可沉默产生血管内皮生长因子(VEGF)的基因。VEGF 在脉络膜新生血管形成(choroidal neo-vascularization, CNV)的发病机制中起着关键作用，而CNV 是湿性年龄相关性黄斑变性(wet age-related macular degeneration, wet AMD)的前兆。
T79010	Lp-PLA2-IN-12	Phospholipase	Metabolism
	Lp-PLA2-IN-12（compound 19）为一种Lp-PLA2抑制剂，主要应用于神经退行性疾病（如AD、青光眼、AMD）及心血管疾病（诸如动脉粥样硬化）的研究。
T75156	Bevasiranib
	Bevasiranib 是一种siRNA，可沉默产生血管内皮生长因子(VEGF)的基因。VEGF 在脉络膜新生血管形成(choroidal neo-vascularization, CNV)的发病机制中起着关键作用，而CNV 是湿性年龄相关性黄斑变性(wet age-related macular degeneration, wet AMD)的前兆。
T76814	Lampalizumab
	Lampalizumab (RG 7417) 为靶向补体通路中补体因子 D (Factor D) 的人源单克隆抗体。通过结合外位点，该药物立体阻断因子 B 进入活性位点，用于老年性黄斑变性 (AMD) 研究。
T74867	UBX1325
	UBX1325 是一种Bcl-xL 抑制剂，可促进衰老细胞的凋亡 (apoptosis)。UBX1325 是一种有效的抗衰老剂，可用于与年龄相关的眼部疾病的研究，如糖尿病性黄斑水肿 (DME)、年龄相关性黄斑变性 (AMD) 和糖尿病性视网膜病变 (DR)。
T79074	Lp-PLA2-IN-14	Phospholipase	Metabolism
	Lp-PLA2-IN-14（Compound 19）是一种选择性的Lp-PLA2抑制剂，其对rhLp-PLA2表现出较高亲和力，pIC50值达到8.4。该化合物主要适用于对抗与神经退行性疾病相关的研究，包括阿尔茨海默病（AD）、青光眼、年龄相关性黄斑变性（AMD），以及心血管疾病如动脉粥样硬化等。
T63192	Lp-PLA2-IN-10
	Lp-PLA2-IN-10 是一种有效的脂蛋白相关磷脂酶 A2 (Lp-PLA2) 抑制剂。Lp-PLA2-IN-10 能够用于神经退行性相关疾病的研究，如阿尔茨海默病(AD)、青光眼、年龄相关的黄斑变性 (AMD)，或者包括动脉粥样硬化等心血管疾病。Lp-PLA2 曾经被称作血小板活化因子乙酰水解酶 (PAF-AH)，是一种参与脂蛋白脂质或磷脂水解的磷脂酶 A2。
T33267	Me6TREN 4HCl Me6TREN Tetrahydrochloride,Me6-TREN Tetrahydrochloride,Me6 4HCl,Me 6 4HCl,Me-6 4HCl
	Me6TREN 4HCl is a potent and efficacious mobilizing agent of hematopoietic stem and progenitor cells (HSPCs) that can act by activating MMP-9 expression and disrupting the SDF-1α/CXCR4 axis, exhibiting more significant mobilizing effects than G-CSF or AMD

化合物

Cat.No: TQ0174

Synonym: AMD-070

Target: CXCR

AMD 3465 hexahydrobromide

Cat.No: T7208

Synonym: GENZ-644494 (hexahydrobromide)

Target: HIV Protease, CXCR

AMD-070 hydrochloride

Cat.No: T22565

Synonym: N-(1H-苯并咪唑-2-基甲基)-N-[(8S)-5,6,7,8-四氢-8-喹啉基]-1,4-丁二胺单盐酸盐

Target: CXCR

Cat.No: T29957

Synonym: AMD 7049

Cat.No: T1776

Synonym: 普乐沙福,JM3100,AMD 3100,AMD-3329

Target: Virus Protease, HIV Protease, CXCR

Cat.No: T29958

Cat.No: T14208

Synonym: GENZ-644494

Target: HIV Protease

Plerixafor octahydrochloride

Cat.No: T1776L

Synonym: 盐酸普乐沙福,JM3100 octahydrochloride,Plerixafor 8HCl (AMD3100 8HCl),Plerixafor 8HCl,SID791 octahydrochloride,AMD 3100 octahydrochloride,JM 3100 8HCl

Target: Virus Protease, HIV Protease, CXCR

Cat.No: T21323

Synonym: NX 473,AMD-473,AMD473,NX-473,NX473,AMD 473

Mavorixafor trihydrochloride

Cat.No: T10296

Synonym: AMD-070 trihydrochloride

Target: HIV Protease

AMD-3451 trihydrochloride

Cat.No: T69583

AMD-3329 hydrobromide

Cat.No: T70260

AMD-3329 free base

Cat.No: T70259

AMD-3451 free base

Cat.No: T69582

Cat.No: T8574

Target: Others

Cat.No: T9928

Target: VEGFR

Cat.No: T23716

Synonym: AMDE 1

Target: Autophagy

Cat.No: T69725

Cat.No: T39327

Synonym: Amdizalisib,HMPL-689

Cat.No: T26615

Synonym: AMDX,DAPD

Amdinocillin methylacetate

Cat.No: T29959

Synonym: Mecillinam acetylmethyl ester

Cat.No: T13157

Synonym: TG100801,TG 100572

Target: VEGFR, Src

Cat.No: T3306

Synonym: PF 04418948,PF04418948

Target: Prostaglandin Receptor

Cat.No: T7493

Synonym: AG-013958,N-[2-氟-5-[[3-[(1E)-2-(2-吡啶基)乙烯基]-1H-吲唑-6-基]氨基]苯基]-1,3-二甲基-1H-吡唑-5-甲酰胺

Target: VEGFR

AG-13958 monohydrochloride

Cat.No: T69452

Cat.No: T28008

Synonym: MDVN 1003,MDVN-1003

Avacincaptad pegol sodium

Cat.No: T74551

Pegaptanib sodium

Cat.No: T39706

CEP dipeptide 1

Cat.No: TP1390

Cat.No: T77016

Risuteganib hydrochloride

Cat.No: TP1464

Cat.No: T76987

Non-PEGylated/naked ARC1905

Cat.No: T74552

Bevasiranib sodium

Cat.No: T75156L

Cat.No: T79010

Target: Phospholipase

Cat.No: T75156

Cat.No: T76814

Cat.No: T74867

Cat.No: T79074

Target: Phospholipase

Cat.No: T63192

Cat.No: T33267

Synonym: Me6TREN Tetrahydrochloride,Me6-TREN Tetrahydrochloride,Me6 4HCl,Me 6 4HCl,Me-6 4HCl

Cat. No.	Product Name	Target	Signaling Pathways
T83915	Norbixin hydrate
	Norbixin是一种在B. orellana中发现的类胡萝卜素，具有多样的生物活性。在无细胞测试中，它与过氧化物酶体增殖物激活受体γ (PPARγ)结合（Ki = 1.15 µM）。在心脑血管代谢综合征大鼠模型中，Norbixin (47.7 mg/kg) 能够减轻高血糖、高胰岛素血症和胰岛素抗性，降低血清脂质水平及心脏中硫代巴比妥酸反应性物质（TBARS）和谷胱甘肽（GSH）的水平。在胆固醇诱导的动脉粥样硬化兔模型中，它降低氧化型LDL和主动脉蛋白氧化水平，并减少动脉粥样硬化面积。Norbixin（每天0.1和1 mg/kg）减少汞诱导的大鼠肝细胞和白细胞DNA损伤。此外，它还能预防与年龄相关的黄斑变性（AMD）Abca4-/- Rdh8-/-小鼠模型中的光感受器退化。

天然产物

Norbixin hydrate

Cat.No: T83915

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