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48

抑制剂 & 化合物

4

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T9023	Atuliflapon AZD5718	FLAP	Immunology/Inflammation
	Atuliflapon (AZD5718) 是可口服的FLAP(5 -脂氧合酶激活蛋白)的抑制剂，IC50值为 2 nM，可用于冠状动脉疾病的研究。
T6033	Zotarolimus ABT-578,佐他莫司,咗他莫司,A 179578	mTOR	PI3K/Akt/mTOR signaling
	Zotarolimus (ABT-578) 是一种免疫抑制剂，是雷帕霉素的衍生物，具有抗增殖活性。它被专门开发作为局部输送支架用于预防冠状动脉再狭窄。
T0005	Aspirin 阿司匹林,Acetylsalicylate,Acetylsalicylic Acid,邻乙酰水杨酸,ASA	Mitophagy; Virus Protease; COX; Autophagy	Autophagy; Immunology/Inflammation; Microbiology/Virology; Neuroscience
	Aspirin (Acetylsalicylic Acid) 是一种选择性 COX 抑制剂，具有多种药理活性。它是组蛋白去乙酰化酶抑制剂，可上调细胞周期阻滞蛋白 p21，抑制携带 COX-1 的卵巢 Y 细胞。它还抑制 HUVEC 和新生大鼠心室心肌细胞中 COX-2 的表达，分别减少 PG 的产生和 ERK 和 NF-KB 的下调。
T0154	Nebivolol hydrochloride R 065824 hydrochloride,盐酸奈必洛尔,Nebivolol HCl,R-65824	Apoptosis; Adrenergic Receptor	Apoptosis; GPCR/G Protein; Neuroscience
	Nebivolol hydrochloride (R 065824 hydrochloride) 是一种β1-肾上腺素受体选择性抑制剂，IC50为0.8 nM。
T19345	GP2-114	Others	Others
	GP2-114 是一种儿茶酚胺运动模拟剂，可用于研究冠状动脉疾病（CAD）。
T8687	diaminohydroxypropanetetraacetic acid	Others	Others
	diaminohydroxypropanetetraacetic acid 已被研究用于治疗血管疾病、冠状动脉疾病、心肌缺血、冠状动脉再狭窄和冠状动脉疾病等。
T24873	TGX-115 TGX 115	PI3K	PI3K/Akt/mTOR signaling
	TGX-115是一种细胞渗透性和有效的PI 3-K 异构体p110β/p110δ抑制剂(对p110β IC50值为 0.13 μM, 对p110δ值为0.63 μM），是一种调节血小板粘附过程的酶，可抑制磷酸肌苷（PI）3-激酶，可用来治疗冠状动脉闭塞、中风、急性冠状动脉综合征、急性心肌梗塞、血管再狭窄、动脉硬化和不稳定心绞痛等心血管疾病。
T1986	Atopaxar E5555,ER-172594-00	Protease-activated Receptor	GPCR/G Protein
	Atopaxar (E5555) 是一种高效、可口服的，选择性的，可逆的凝血酶受体蛋白酶激活受体-1 (PAR-1) 拮抗剂。它是一种抗血小板剂，能干扰血小板信号，可用于动脉粥样硬化血栓性疾病的研究。
T22787	FPL 55712	LTR	Immunology/Inflammation
	FPL 55712 是白三烯受体和 SRS-A 拮抗剂，抑制支气管收缩，可用于研究哮喘和冠状动脉血栓。
T32155	Indecainide Ricainide,Ricainid,Decabid,Indecainidum,Indecainida	Others	Others
	Indecainide (Ricainid) 是一种新型抗心律失常化合物，具有致癌性，可用于研究继发于冠状动脉疾病或心肌病的慢性稳定型室性心律失常。
T4179	Probucol disuccinate	LDL	Metabolism
	Probucol disucinate 是一种 Probucol 的衍生物。其中 Probucol 是脂质调节的化合物，它能降低 LDL-cholesterol 水平。
T2480	Apabetalone RVX-208,RVX000222,阿帕他隆	Epigenetic Reader Domain; HIV Protease	Chromatin/Epigenetic; Microbiology/Virology; Proteases/Proteasome
	Apabetalone (RVX000222) 是一种 BET 溴结构域抑制剂，用于研究治疗糖尿病、动脉粥样硬化和冠状动脉疾病。
T61028	Mitiperstat AZD4831	Glutathione Peroxidase	Metabolism
	Mitiperstat 是一种强效的骨髓过氧化物酶（MPO）抑制剂。Mitiperstat 对预防如心力衰竭和冠状动脉疾病类的心血管疾病有很好的效果。
T10595	BQ-788 BQ788	Endothelin Receptor	GPCR/G Protein
	BQ-788 是一种具有选择性和有效性的 ETB 受体拮抗剂，具有潜在的高血压活性，抑制 ET-1 与 ETB 受体结合，抑制外源性 ET-1 诱导的冠状动脉灌注压升高。
T4287	Succinobucol Probucol monosuccinate,AGI-1067	Antioxidant; Reactive Oxygen Species	Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction
	Succinobucol (Probucol monosuccinate) 是酚类抗氧化剂，具有抗炎、抗血小板聚集活性。
T10364	Arbutamine GP 21213	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Arbutamine (GP 21213) 是一种新型非选择性β-肾上腺素受体激动剂，具有α-1-拟交感神经活性。Arbutamine 促进心脏应激，增加心率、心脏收缩力。Arbutamine 可用于研究心脏应激和冠状动脉疾病。
T0182L2	(±) Clopidogrel hydrogen sulfate 硫酸氢氯吡格雷,Plavix,Clopidogrel hydrogen sulfate,Iscover	P2Y Receptor	GPCR/G Protein; Neuroscience
	(±) Clopidogrel hydrogen sulfate (Iscover) 是一种在药理学和结构上类似于ticlopidine 的抗血小板药物，用于抑制脑血管疾病、外周血管疾病和冠状动脉疾病等各种疾病中的血栓。
T31992	Granotapide	CETP	Metabolism
	Granotapide 是一种微粒体甘油三酯转移蛋白（MTP）抑制剂，治疗和而预防动脉硬化，冠状动脉疾病，代谢综合征，肥胖，糖尿病，糖尿病前期和高血压。
T5856	Barnidipine hydrochloride 盐酸巴尼地平,YM-09730-5 hydrochloride,Mepirodipine (hydrochloride)	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Barnidipine hydrochloride (YM-09730-5 hydrochloride) 是一种二氢吡啶类钙通道阻滞剂，对 CaA 受体具有选择性作用。它是一种抗高血压药物，通过减少其血管扩张作用继发的外周血管阻力起作用。
T4567	Sulfaphenazole Plisulfan,Raziosulfa,Depocid,磺胺苯吡唑,Depotsulfonamide	P450; Antibacterial	Metabolism; Microbiology/Virology
	Sulfaphenazole (Plisulfan) 是一种 CYP2C9的特异性抑制剂，抑制 CYP2C9介导的亚油酸动脉粥样硬化和促炎症效应，增加 AP-1的氧化应激和激活。
T73695	Canakinumab ACZ 885,Ilaris	IL Receptor	Immunology/Inflammation
	Canakinumab (ACZ885) 是一种重组人靶向 IL-1β 单克隆抗体。Canakinumab 显示出对人类和绒猴 IL-1β 具有抑制作用， IC50 值为分别为 43.6 和 40.8 pM。Canakinumab 具有抗炎活性，通过中和 IL-1β 信号来抑制与自身免疫性疾病相关的炎症。Canakinumab 可用于治疗痛风和冠状动脉疾病。
T14390L	(2R,3S)-Azelaprag	Apelin receptor	GPCR/G Protein
	(2R,3S)-N-(4-(2,6-dimethoxyphenyl)-5-(5-methylpyridin-3-yl)-4H-1,2,4-triazol-3-yl)-3-(5-methylpyrimidin-2-yl)butane-2-sulfonamide 是一种Apelin 受体激动剂，对Apelin 受体的EC50为0.012 µM。(2R,3S)-N-(4-(2,6-dimethoxyphenyl)-5-(5-methylpyridin-3-yl)-4H-1,2,4-triazol-3-yl)-3-(5-methylpyrimidin-2-yl)butane-2-sulfonamide 可用于治疗心力衰竭、动脉粥样硬化、肥胖、糖尿病、肌萎缩侧索硬化、冠心病、高血压、中风和心肌梗塞等疾病。
T30255	AZD2716 AZD 2716,AZD-2716
	AZD2716 is an effective selective phospholipase A2 inhibitor for the treatment of coronary artery and cardiovascular disease.
T27351	Fostedil KB-944,KB944,A 53986,KB 944,A-53986,BRN 3626546
	Fostedil is a calcium channel antagonist. KB-944 increased regional segment function in normal and ischemic regions and maintained distal coronary artery perfusion pressure, coronary flow and transmural regional myocardial blood flow during partial corona
T26739	Batifiban
	Batifiban, a glycoprotein IIb/IIIa antagonist, is used potentially for the treatment of coronary artery disease.
T69970	AZD5718
	AZD5718 is a potent and selective FLAP inhibitor (IC50 = 2.0 nM) for Treatment of Coronary Artery Disease. AZD5718 demonstrated a dose dependent and greater than 90% suppression of leukotriene production over 24 h. Preclinical toxicology studies in rat and dog did not show any serious adverse events of clinical significance. Currently, AZD5718 is evaluated in a phase 2a study for treatment of coronary artery disease.
T41029	Streptokinase
	Streptokinase is a bacterial protein that acts as a plasminogen activator, commonly employed in the investigation of blood-clotting disorders. Its application extends to enhancing reperfusion blood flow after coronary artery occlusion.
T1986L	Atopaxar Hydrobromide	Protease-activated Receptor	GPCR/G Protein
	Atopaxar hydrobromide 是可口服的，高效选择性的可逆凝血酶受体蛋白酶激活受体-1 拮抗剂。它是一种抗血小板剂，能干扰血小板信号，用于动脉粥样硬化血栓性疾病的研究。
T68639	Ciprostene (free base)
	Ciprostene (free base) is a synthetic, chemically stable analog of prostacyclin (PGI2). In animal models, administration of ciprostene resulted in dose-dependent hypotension, tachycardia, and inhibition of ex vivo ADP-induced platelet aggregation. Ciprostene was evaluated in clinical trials in patients with peripheral vascular disease. It was found to reduce restenosis in patients with coronary artery disease undergoing therapeutic percutaneous transluminal coronary angioplasty.
T71402	Nicorandil-d4
	Nicorandil-d4 is intended for use as an internal standard for the quantification of nicorandil by GC- or LC-MS. Nicorandil is an activator of sulfonylurea receptor 2B (SUR2B) linked to ATP-sensitive potassium channel Kir6.2 (EC50 = ~10 µM) and a nitric oxide (NO) donor. It is selective for SUR2B/Kir6.2 over the SUR2A/Kir6.2 channel (EC50 = >500 µM). Nicorandil activates soluble guanylate cyclase in a cell-free assay and relaxes partially depolarized isolated bovine coronary artery strips (EC50 =...
TP2119	Sarafotoxin S6a
	Endothelin receptor agonist (EC50 values are 7.5 and > 150 nM for contraction of pig coronary artery and guinea pig aorta respectively). Nociceptive in vivo.
T79239	PCSK9-IN-19
	PCSK9-IN-19 (Compound 1)作为一种PCSK9抑制剂，用于研究高LDL胆固醇水平及预防冠状动脉疾病。
T76302	[Lys4] Sarafotoxin S6c
	[Lys4] Sarafotoxin S6c 是一种 sarafotoxin 类似物，是一种有效的内皮素受体 (endothelin receptor) 的部分激动剂。[Lys4] Sarafotoxin S6c 可诱导猪冠状动脉收缩，其 EC50为 1.5 nM。
T75807	Sarafotoxin S6a TFA
	Sarafotoxin S6a TFA 是一种 Sarafotoxin 类似物，是一种内皮素受体 (endothelin receptor) 激动剂，具有与 Endothelin-3 相似的 ETA/ETB 选择性。Sarafotoxin S6a TFA 诱导猪冠状动脉的 EC50值为 7.5 nM。
T24690	Pyrromecaine HCl Bumecaine hydrochloride,Pyrromecaine
	Pyrromecaine is a local anesthetic used for surface anesthesia. Pyromecaine has a wide spectrum of antiarrhythmic action, exerts a favorable effect on the contractility of the left ventricle, and on the myocardial blood flow following the ligation of the
T35463	(±)14(15)-EET (±)14,15-EET,(±)14,15-EpETrE,(±)14(15)-EET
	(±)14(15)-EET is a metabolite of arachidonic acid that is formed via epoxidation of arachidonic acid by cytochrome P450.[1],[2] It prevents increases in leukotriene B4, ICAM-1, and chemokine (C-C motif) ligand 1 (CCL2) induced by oxidized LDL in primary rat pulmonary artery endothelial cells (RPAECs) when used at a concentration of 1 μM.[3] (±)14(15)-EET induces dilation of preconstricted isolated canine coronary arterioles (EC50 = 0.2 pM).[4] It reduces myocardial infarct size as a percentage o...
T60901	S(-)-Bisoprolol
	S(-)-Bisoprolol 是 Bisoprolol 的 S(-)-对映异构体。Bisoprolol 在高血压，冠状动脉疾病和稳定的心室功能不全的研究方面具有潜力。Bisoprolol 是一种有效的选择性的，口服活性的 β1 肾上腺素受体阻滞剂，对 β2 受体几乎没有活性。
T36547	Quazinone
	Quazinone is a selective inhibitor of phosphodiesterase 3 (PDE3) with positive inotropic and vasodilating properties.1,2 It induces relaxation of precontracted isolated human cavernous smooth muscle (IC50 = 4.2 μM).1 Quazinone (10-300 μg/kg) increases myocardial contractile force in anesthetized open-chest dogs in a dose-dependent manner, as well as decreases systolic and diastolic blood pressure.2 It also inhibits DNA synthesis induced by the PDGF isoform PDGF-BB in bovine coronary artery smoot...
T68297	Dilmapimod tosylate
	Dilmapimod tosylate is a potent p38 mitogen-activated protein kinase (MAPK) inhibitor. It was investigated for its anti-inflammatory effect in non-head injury trauma patients at risk for developing acute respiratory distress syndrome. IL-1β was identified as a gene regulated by dilmapimod that could influence c-reactive protein levels. Dilmapimod had been in phase III clinical trials by GlaxoSmithKline for the treatment of rheumatoid arthritis, neuropathic pain, coronary artery disease (CAD) and...
T74156	S(-)-Bisoprolol fumarate
	S(-)-Bisoprolol fumarate 是 Bisoprolol fumarate 的 S(-)-对映异构体，这种化合物是一种有效的、选择性的，并具有口服活性的 β1 肾上腺素受体 (β1-adrenergic receptor) 阻滞剂，对 β2 受体的活性较低。它主要用于研究高血压、冠状动脉疾病和稳定的心室功能障碍。
T73083	Nipradolol KT 210 ; K 351 ; Hypadil,Hypadil,KT 210,K 351
	Nipradolol (KT-210; K-351) 是一种有效的 α-1-肾上腺素能受体的阻滞剂。Nipradolol 还抑制白化兔模型中 Phenylephrine 诱导的眼压升高 (IOP)。Nipradolol 抑制去甲肾上腺素 (NA) 引起的肌肉收缩，对犬冠状动脉也有血管扩张剂活性。
T63035	Izilendustat hydrochloride
	Izilendustat (hydrochloride) 是一种脯氨酰羟化酶 (prolyl hydroxylase) 的有效抑制剂，能够稳定缺氧诱导因子-1 α (HIF-1α) 和缺氧诱导因子-2 (HIF-2)。Izilendustat (hydrochloride) 具有潜力进行 HIF-1α 相关疾病的研究（包括外周血管疾病（PVD）、心力衰竭、冠状动脉疾病（CAD）、缺血、贫血、结肠炎和其他炎症性肠病）。
T21485	Perindopril
	Perindopril (S-9490) 是一种长效血管紧张素转换酶（ACE）抑制剂，用于治疗高血压、心力衰竭或稳定性冠状动脉疾病。
T17231	Vicagrel	Others	Others
	Vicagrel 是一种有效的、具有口服活性抗血小板化合物，通过不可逆地抑制 P2Y12 受体，降低代谢失活，增强了阿司匹林对啮齿类动物血小板聚集和血栓形成起抑制作用。Viagrel 可用于治疗冠状动脉疾病、外周血管疾病和脑血管疾病中血栓。
T81451	PKCd (8-17)
	PKCd (8-17) 是源自蛋白激酶 C (PKC)d V1 结构域的生物活性肽。它能抑制由佛波醇 12-肉豆蔻酸酯 13-乙酸酯 (PMA) 诱导的 PKCd 易位和激活。此外，PKCd (8-17) 在降低心脏和脑细胞缺血损伤、促进成纤维细胞增殖、以及抑制小鼠移植冠状动脉疾病方面具有潜在应用。
T36221	2-chloro Palmitic Acid
	2-chloro Palmitic acid is a monochlorinated form of palmitic acid . It is produced in a myeloperoxidase (MPO) and time-dependent manner in neutrophils stimulated by phorbol 12-myristate 13-acetate . 2-chloro Palmitic acid (10 μM) induces neutrophil extracellular trap (NET) formation (NETosis) in human neutrophils, increasing DNA release from neutrophils, colocalization of MPO with extracellular DNA (ecDNA), and trapping of E. coli. It increases COX-2 protein levels in human coronary artery endot...
T35598	Neuromedin U-25 (human) (trifluoroacetate salt)
	Neuromedin U (NMU) is a neuropeptide first demonstrated to drive smooth muscle contraction.1Translated as a 174 amino acid propeptide, NMU is cleaved to different lengths in different animals. It has diverse receptor-mediated rolesin vivo, as it regulates feeding, vasoconstriction, nociception, and bone remodeling and contributes to obesity, cancer and septic shock.2,2NMU-25 is the active form of NMU in humans. It binds with high affinity to receptors on human left ventricle and coronary artery ...
T83769	TC 14012 hydrochloride H-Arg-Arg-Nal-Cys-Tyr-Cit-Lys-D-Cit-Pro-Tyr-Arg-Cit-Cys-Arg-NH2
	TC 14012是一种化学肽模拟的拮抗剂，针对趋化因子(C-X-C motif)受体4（CXCR4；IC50 = 2.9 nM）和CXCR7激动剂。它能在表达CXCR7的HEK293T细胞中诱导β-arrestin招募（EC50 = 350 nM）。TC 14012可减少HIV在MT-4细胞中的细胞病理效应（EC50 = 0.4 nM），并以CXCR4依赖的方式抑制HIV在体外进入（IC50 = 19.3 nM）。它还能抑制由趋化因子(C-X-C motif)配体12（CXCL12）在MDA-MB-231乳腺癌细胞和人脐静脉内皮细胞（HUVECs）中诱导的迁移，当使用浓度范围从10到1,000 nM时。在通过左前降（LAD）冠状动脉结扎诱导的急性心肌梗死小鼠模型中，TC 14012（10 mg/kg）能减少梗死面积。

化合物

Cat.No: T9023

Synonym: AZD5718

Target: FLAP

Cat.No: T6033

Synonym: ABT-578,佐他莫司,咗他莫司,A 179578

Target: mTOR

Cat.No: T0005

Synonym: 阿司匹林,Acetylsalicylate,Acetylsalicylic Acid,邻乙酰水杨酸,ASA

Target: Mitophagy, Virus Protease, COX, Autophagy

Nebivolol hydrochloride

Cat.No: T0154

Synonym: R 065824 hydrochloride,盐酸奈必洛尔,Nebivolol HCl,R-65824

Target: Apoptosis, Adrenergic Receptor

Cat.No: T19345

Target: Others

diaminohydroxypropanetetraacetic acid

Cat.No: T8687

Target: Others

Cat.No: T24873

Synonym: TGX 115

Target: PI3K

Cat.No: T1986

Synonym: E5555,ER-172594-00

Target: Protease-activated Receptor

Cat.No: T22787

Target: LTR

Cat.No: T32155

Synonym: Ricainide,Ricainid,Decabid,Indecainidum,Indecainida

Target: Others

Probucol disuccinate

Cat.No: T4179

Target: LDL

Cat.No: T2480

Synonym: RVX-208,RVX000222,阿帕他隆

Target: Epigenetic Reader Domain, HIV Protease

Cat.No: T61028

Synonym: AZD4831

Target: Glutathione Peroxidase

Cat.No: T10595

Synonym: BQ788

Target: Endothelin Receptor

Cat.No: T4287

Synonym: Probucol monosuccinate,AGI-1067

Target: Antioxidant, Reactive Oxygen Species

Cat.No: T10364

Synonym: GP 21213

Target: Adrenergic Receptor

(±) Clopidogrel hydrogen sulfate

Cat.No: T0182L2

Synonym: 硫酸氢氯吡格雷,Plavix,Clopidogrel hydrogen sulfate,Iscover

Target: P2Y Receptor

Cat.No: T31992

Target: CETP

Barnidipine hydrochloride

Cat.No: T5856

Synonym: 盐酸巴尼地平,YM-09730-5 hydrochloride,Mepirodipine (hydrochloride)

Target: Calcium Channel

Cat.No: T4567

Synonym: Plisulfan,Raziosulfa,Depocid,磺胺苯吡唑,Depotsulfonamide

Target: P450, Antibacterial

Cat.No: T73695

Synonym: ACZ 885,Ilaris

Target: IL Receptor

(2R,3S)-Azelaprag

Cat.No: T14390L

Target: Apelin receptor

Cat.No: T30255

Synonym: AZD 2716,AZD-2716

Cat.No: T27351

Synonym: KB-944,KB944,A 53986,KB 944,A-53986,BRN 3626546

Cat.No: T26739

Cat.No: T69970

Cat.No: T41029

Atopaxar Hydrobromide

Cat.No: T1986L

Target: Protease-activated Receptor

Ciprostene (free base)

Cat.No: T68639

Cat.No: T71402

Sarafotoxin S6a

Cat.No: TP2119

Cat.No: T79239

[Lys4] Sarafotoxin S6c

Cat.No: T76302

Sarafotoxin S6a TFA

Cat.No: T75807

Pyrromecaine HCl

Cat.No: T24690

Synonym: Bumecaine hydrochloride,Pyrromecaine

Cat.No: T35463

Synonym: (±)14,15-EET,(±)14,15-EpETrE,(±)14(15)-EET

S(-)-Bisoprolol

Cat.No: T60901

Cat.No: T36547

Dilmapimod tosylate

Cat.No: T68297

S(-)-Bisoprolol fumarate

Cat.No: T74156

Cat.No: T73083

Synonym: KT 210 ; K 351 ; Hypadil,Hypadil,KT 210,K 351

Izilendustat hydrochloride

Cat.No: T63035

Cat.No: T21485

Cat.No: T17231

Target: Others

Cat.No: T81451

2-chloro Palmitic Acid

Cat.No: T36221

Neuromedin U-25 (human) (trifluoroacetate salt)

Cat.No: T35598

TC 14012 hydrochloride

Cat.No: T83769

Synonym: H-Arg-Arg-Nal-Cys-Tyr-Cit-Lys-D-Cit-Pro-Tyr-Arg-Cit-Cys-Arg-NH2

Cat. No.	Product Name	Target	Signaling Pathways
TN6715	7-Ketocholesterol	Others	Others
	7-Ketocholesterol 是胆固醇的代谢物。
S00015	Tea polyphenol	Apoptosis; Others; Autophagy	Apoptosis; Autophagy; Others
	Tea polyphenol 也称为绿茶提取物，是茶中天然存在的酚类化合物，具有抗癌、抗氧化、抑制细胞增殖、诱导细胞凋亡、延缓细胞周期和调节致癌物代谢等生物活性。
T4S1422	Praeruptorin E 白花前胡素 E,白花前胡素E	Others; Calcium Channel	Membrane transporter/Ion channel; Metabolism; Others
	Praeruptorin E 是白花前胡中的一种主要成分，是钙拮抗剂，pD2′值为 5.2。
TN2533	1-Hydroxy-2,3,4,7-tetramethoxyxanthone	5-HT Receptor	GPCR/G Protein; Neuroscience
	1-Hydroxy-2,3,4,7-tetramethoxy-xanthone has vasodilatory action, it can cause vasodilation in the coronary artery pre-contracted with 1uM 5-hydroxytryptamine (5-HT), with the EC 50 value of 6.6±1.4 uM. 1-Hydroxy-2,3,4,7-tetramethoxyxanthone can effectivel

天然产物

7-Ketocholesterol

Cat.No: TN6715

Target: Others

Cat.No: S00015

Target: Apoptosis, Others, Autophagy

Cat.No: T4S1422

Synonym: 白花前胡素 E,白花前胡素E

Target: Others, Calcium Channel

1-Hydroxy-2,3,4,7-tetramethoxyxanthone

Cat.No: TN2533

Target: 5-HT Receptor

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