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87

抑制剂 & 化合物

13

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T13173	TMPA	Others; AMPK	Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling
	TMPA 是一种核受体 Nur77 和 LKB1 相互作用的拮抗剂。
T8944	TTA-A2	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	TTA-A2 是一种选择性 T 型钙通道拮抗剂，是一种有效的抗惊厥药，可减少孕烷 X 受体的激活。它对 Cav3.1 (a1G) 和 Cav3.2 (a1H) 通道在 -80 mV 和- 100 mV 保持电位上具有同样的作用，IC50 值分别为 89 和 92 nM。它可用于多种人类神经系统疾病的研究，包括睡眠障碍和癫痫。
T0283	Trimethadione 三甲双酮,3,5,5,-Trimethyloxazolidine-2,4-dione	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Trimethadione (3,5,5,-Trimethyloxazolidine-2,4-dione) 是恶唑烷二酮类抗惊厥剂，也是一种 T 型钙通道阻滞剂，具有抗痛觉过敏作用，可用于研究失神发作。
T64203	T-Type calcium channel inhibitor 2
	T-Type calcium channel inhibitor 2 (compound 6g) 是一种 T 型钙通道的有效抑制剂，能够作用于 Cav3.1 (α1G) (IC50: 31.0 μM)、Cav3.2 (α1H) (IC50: 83.1 μM)、Cav3.3 (α1I) (α1H) (IC50: 69.3 μM)。T-Type calcium channel inhibitor 2 对 A549、HCT-116 细胞表现出细胞毒性，IC50s 分别为5.0、6.4 μM。
T12032	Mibefradil dihydrochloride 盐酸米贝地尔,Ro 40-5967 (dihydrochloride),米贝拉地尔	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Mibefradil dihydrochloride (Ro 40-5967 (dihydrochloride)) 是一种钙离子通道抑制剂，选择性作用于 T 型 Ca2+通道，对 T 型和 L 型通道的IC50分别为 2.7 和 18.6 μM。
T71990	TTA-A8	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	TTA-A8 是 T 型钙通道的拮抗剂。
T3703	ABT-639 ABT 639	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	ABT-639 是一种有效的选择性 T 型钙通道阻滞剂。
T26174	SAK3 SAK 3,SAK-3	Calcium Channel; AChR	Membrane transporter/Ion channel; Metabolism; Neuroscience
	SAK3 是一种新型的 nAChR 活性调节剂，可增强 T 型电压门控 Ca2+ 通道 (T-VGCC) 的活性，对 Cav3.1 和 Cav3.3 T 型 Ca2+ 通道电流均有增强作用。SAK3 对人神经母细胞瘤 SH-SY5Y 细胞中东莨菪碱诱导的胆碱能功能障碍有神经保护作用。SAK3 可用于研究记忆缺陷和阿尔茨海默病。
T2323	Efonidipine (±)-Efonidipine,NZ-105,依福地平	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Efonidipine (NZ-105) 是一种二氢吡啶类钙通道阻滞剂，可阻断 T 型和 L 型钙通道。
T5632	Suvecaltamide MK-8998	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Suvecaltamide (MK-8998) 是一种选择性的 T 型钙通道抑制剂。
T6571	Lomerizine dihydrochloride Terranas,盐酸洛美利嗪,Lomerizine 2HCl,Lomerizine hydrochloride,KB-2796	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Lomerizine dihydrochloride (KB-2796) 是双重 L 和 T 型电压门控钙通道拮抗剂。
T12238	NNC 55-0396 NNC 55-0396 dihydrochloride	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	NNC 55-0396 是一种高特异性的 T 型钙通道阻滞剂，IC50 为 6.8 μM。 NNC 55-0396 可用于预防人类卵巢癌细胞增殖的研究。
T8448	ZSET1446 ZSET-1446,ST-101	Calcium Channel; AChR	Membrane transporter/Ion channel; Metabolism; Neuroscience
	ZSET1446 (ST-101) 是一种 T 型钙通道激活剂，用于治疗各类阿尔茨海默病 (AD) 模型中的学习缺陷。
T29201	Z944 Z 944,Z-944	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Z944 是有效的 T 型钙通道拮抗剂，对跨模态和视觉识别记忆障碍有缓解作用。
T23411L	T-0156 T 0156	PDE; Parasite	Metabolism; Microbiology/Virology
	T-0156 是一种新型高效且具有选择性的 5 型磷酸二酯酶抑制剂，抑制环磷酸鸟苷 (cGMP) 的水解，对 PDE6、PDE1、PDE2、PDE3 和 PDE4 较低的亲和力。
T64387	2-Nitrobenzoic acid o-Nitrobenzoic acid	Others	Others
	2-Nitrobenzoic acid (o-Nitrobenzoic acid) 是一种抗增殖化合物，对表达 T 型钙通道α1H 或其剪接变体δ25的 jurkat 细胞系显示出8.3μM 的 IC50。
T37427	(2R/S)-6-PNG 6-Prenylnaringenin,(±)-6-Prenylnaringenin	Calcium Channel; HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism
	(2R/S)-6-PNG (6-Prenylnaringenin) 是新型天然组蛋白脱乙酰酶抑制剂，具有抗癌抗肿瘤活性，可阻断T型钙通道可减轻小鼠的神经性和内脏疼痛。
T68123	Oxodipine	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Oxodipine 是一种二氢吡啶型钙拮抗剂，抑制了KCl 诱导的兔主动脉收缩，降低了效力较低的大鼠心室试纸收缩的心脏力量。在大鼠培养的新生儿心室肌细胞中，Oxodipine 降低了L 型Ca 电流（I），IC 为0.24μM，对T 型Ca 电流（I）的IC 为0.41μM。Oxodipine 会使小鼠便秘和狗牙龈增生。
T13219	TTA-Q6	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	TTA-Q6 是一种选择性 T 型 Ca2+ 通道拮抗剂，具有潜在的抗肿瘤和免疫调节活性，可抑制肿瘤细胞摄取细胞外钙离子，诱导细胞内钙缺乏和内质网（ER）应激，用于治疗神经系统疾病。
T10570	Fostemsavir Tris BMS-663068 Tris	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	Fostemsavir Tris (BMS-663068 Tris) 是一种 HIV-1附着抑制剂。
T9906	Ipilimumab	Others	Others
	Ipilimumab 是全人类单克隆抗体 IgG1κ，能够抗 CTLA-4。其中CTLA-4是一种由活化的 T 细胞产生的免疫抑制分子。
T0267	Zonisamide AD 810,唑尼沙胺,CI 912	Calcium Channel; Sodium Channel; Carbonic Anhydrase	Membrane transporter/Ion channel; Metabolism
	Zonisamide (AD 810) 是锌酶碳酸酐酶 (carbonic anhydrase) 的有效抑制剂，对人类线粒体同工酶 hCA II 和 hCA V 作用的 Ki 值分别为 35.2 nM 和 20.6 nM。Zonisamide 具有抗癫痫活性，在癫痫、癫痫发作和帕金森病的研究中具有价值。
TQ0153	Mibefradil 米贝地尔,Ro 40-5967	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Mibefradil is a calcium channel blocker with moderate selectivity for T-type Ca2+ channels (IC50s: 2.7 μM and 18.6 μM for T-type and L-type currents).
T71202	A-1048400
	A-1048400 is a potent and selective N-type and T-type calcium channel blocker.
T33891	PBI-1393 PBI1393,BCH1393,BCH 1393,BCH-1393,PBI 1393
	PBI-1393 can be used as an enhancer for Th1 type cytokine production and primary T cell activation.
T62402	TTA-P2
	TTA-P2 (T-Type calcium channel inhibitor) 是一种 T 型钙通道的有效抑制剂。TTA-P2 能够有效的穿透 CNS 并阻断小脑深部核神经元中的天然 T 型电流，完全消除野生型和突变型 Cav3.1 通道的窗口电流。TTA-P2 具有潜力进行神经疾病的研究。
T80496	Kurtoxin	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Kurtoxin是一种选择性Cav3 (T-type) 电压门控Ca2+通道抑制剂，对Cav3.1 (α1G T-type) Ca2+通道的Kd值为15 nM。该化合物与中枢和外周神经元的L型、N型和P型Ca2+通道有高度亲和性，并对电压门控Na+通道也有交叉反应性。
T13220	TTA-Q6(isomer)	Others	Others
	TTA-Q6(isomer) is an isomer of TTA-Q6. TTA-Q6 is a selective antagonist of the T-type Ca2+ channel.
T25874	NMP-7 NMP7,NMP 7
	NMP-7 is a non-selective CB1 and CB2 cannabinoid receptor agonist that works by blocking T-type calcium channels.
T24738	RQ-00311651
	RQ-00311651 is a novel T-type Ca2+ channel blocker. RQ-00311651 also inhibited high K-induced Ca signaling in those cells.
T12076	ML218 hydrochloride	Others	Others
	ML218 hydrochloride is a selective and orally active T-type Ca2+ channels (Cav3.1, Cav3.2, Cav3.3) inhibitor (Cav3.2 and Cav3.3 with IC50s of 310 nM and 270 nM , respectively).
T69809	NNL-2
	NNL-2 is a synthetic cannabinoid and T-type calcium channel inhibitor. This product is for research use only.
T63312	ABT-639 hydrochloride
	ABT-639 hydrochloride 是选择性的、新型的 T 型 Ca2+通道阻滞剂。
T61393	IAA65
	IAA65 是一种有效的 T 型钙通道抑制剂 (T-type calcium channel)，IC50值为 18.9 μM。IAA65 可用于癫痫研究。
T14120	ACT-709478	Others	Others
	ACT-709478 is a potent, selective T-type calcium channel blocker that is orally active and capable of penetrating the brain. It is currently utilized in research focusing on generalized epilepsies[1].
T60648	IAB15
	IAB15 是可用于癫痫研究的，T 型钙通道的有效抑制剂。
T63350	Cav 3.2 inhibitor 3
	Cav 3.2 inhibitor 3 是 Cav3.2 T-type Ca2+channel 的有效抑制剂 (IC50: 0.1534 μM)，且对 D2受体的结合亲和力很低。
T75792	Huwentoxin XVI TFA
	Huwentoxin XVI TFA，一种来自鸟蛛 Ornithoctonus huwena 的止痛剂，一种高度可逆和选择性的哺乳动物 N 型钙通道 (N-type calcium channel) (IC50约为 60 nM) 拮抗剂。Huwentoxin XVI TFA 对电压门控的 T 型钙通道，钾通道或钠通道没有影响。
T40590	NY-ESO-1 (87-111)
	NY-ESO-1 (87-111) is a pan-MHC class II-restricted peptide that interacts with various HLA-DR and HLA-DP4 molecules, inducing activation of CD4+ T cells with Th1-type and Th-2/Th0-type responses, when presented in conjunction with HLA-DR and HLA-DP4 molecules.
T37966	T-91825
	T-91825 (PPI-0903M) is a potent N-phosphono-type cephalosporin compound, which serves as the active variant of TAK-599. It exhibits broad-spectrum activity against both gram-positive and gram-negative bacteria [1][2].
T62876	MONIRO-1
	MONIRO-1 是一种 T 型和 N 型钙通道阻断剂，作用于 hCav2.2 (IC50: 34 μM)、hCav3.1 (IC50: 3.3 μM)、hCav3.2 (IC50: 1.7 μM) 和 hCav3.3 (IC50: 7.2 μM)。
T26968	CCT036477 CCT 036477,CCT-036477
	CCT036477 is a selective inhibitor of wingless-type MMTV integration site family dependent transcription. CCT036477reduces the transcriptional activity of the T-cell factor and lymphoid enhancer factor transcription factor family at the ß-catenin level.
TQ0007L	Cintirorgon sodium LYC-55716 sodium salt,LYC 55716,LYC55716
	Cintirorgon (LYC-55716) is an orally active RORgamma agonist with potential immunomodulatory and antineoplastic activities. LYC-55716 selectively binds to the RORg, and binds to ROR response elements, enhancing the function, proliferation, and survival of
T11730	JTT 551	Others	Others
	JTT 551 can be used in the research of type 2 diabetes mellitus. JTT 551 is selective a protein tyrosine phosphatase 1B (PTP1B) inhibitor, with Kis of 0.22 μM and 9.3 μM for PTP1B and TCPTP (T-cell protein tyrosine phosphatase), respectively.
T81697	NBI-6024
	NBI-6024 是一种变构肽配体(APL)，可被1型糖尿病患者中产生炎症性干扰素-γ的T辅助淋巴细胞识别的表位。
T63606	Cav 3.2 inhibitor 2
	Cav 3.2 inhibitor 2 是一种 Cav3.2 T-type Ca2+channels 的抑制剂，-80mV 恒定电位下，其IC50=0.09339 μM。Cav 3.2 inhibitor 2 对小鼠 T 通道依赖性的躯体和内脏疼痛表现出有效的抑制作用。Cav 3.2 inhibitor 2 能够用于研究顽固性疼痛。
T29033	U-7524 2-Aminooxyacetic acid,U 7524,Aminooxyacetic acid,U7524,AOAA
	U-7524, also known as AOAA and Aminooxyacetic acid, is an inhibitor of 4-aminobutyrate aminotransferase (GABA-T). AOAA is also a general inhibitor of pyridoxal phosphate (PLP)-dependent enzymes (this includes GABA-T). It functions as an inhibitor by attac
T61747	TTA-P1
	TTA-P1 is a highly potent compound that effectively inhibits human T-type calcium channels, which are involved in various physiological processes such as neuronal burst firing, hormone secretion, and cell growth. With its unique state-independent properties, TTA-P1 holds promising potential for advancing research on absence epilepsy [1].
T78291	Tregalizumab BT-061
	Tregalizumab为人源化抗CD4单克隆抗体（IgG1型），体外能选择性激活调节性T细胞（Tregs）功能。适用于研究自身免疫性疾病（因Treg功能不足）及过敏反应。
T36858	C12 Galactosylceramide (d18:1/12:0)
	C12 Galactosylceramide is a bioactive sphingolipid. It inhibits IL-4 production by 53.84% in EL4 T cells when used at a concentration of 10 μM. C12 Galactosylceramide reduces the growth of human papillomavirus type 16-associated tumors in mice and reduces tumor recurrence following surgical removal or chemotherapy. It also reduces natural killer T cell activity, delays the onset of proteinuria, and improves survival in a mouse model of systemic lupus.

化合物

Cat.No: T13173

Target: Others, AMPK

Cat.No: T8944

Target: Calcium Channel

Cat.No: T0283

Synonym: 三甲双酮,3,5,5,-Trimethyloxazolidine-2,4-dione

Target: Calcium Channel

T-Type calcium channel inhibitor 2

Cat.No: T64203

Mibefradil dihydrochloride

Cat.No: T12032

Synonym: 盐酸米贝地尔,Ro 40-5967 (dihydrochloride),米贝拉地尔

Target: Calcium Channel

Cat.No: T71990

Target: Calcium Channel

Cat.No: T3703

Synonym: ABT 639

Target: Calcium Channel

Cat.No: T26174

Synonym: SAK 3,SAK-3

Target: Calcium Channel, AChR

Cat.No: T2323

Synonym: (±)-Efonidipine,NZ-105,依福地平

Target: Calcium Channel

Cat.No: T5632

Synonym: MK-8998

Target: Calcium Channel

Lomerizine dihydrochloride

Cat.No: T6571

Synonym: Terranas,盐酸洛美利嗪,Lomerizine 2HCl,Lomerizine hydrochloride,KB-2796

Target: Calcium Channel

Cat.No: T12238

Synonym: NNC 55-0396 dihydrochloride

Target: Calcium Channel

Cat.No: T8448

Synonym: ZSET-1446,ST-101

Target: Calcium Channel, AChR

Cat.No: T29201

Synonym: Z 944,Z-944

Target: Calcium Channel

Cat.No: T23411L

Synonym: T 0156

Target: PDE, Parasite

2-Nitrobenzoic acid

Cat.No: T64387

Synonym: o-Nitrobenzoic acid

Target: Others

Cat.No: T37427

Synonym: 6-Prenylnaringenin,(±)-6-Prenylnaringenin

Target: Calcium Channel, HDAC

Cat.No: T68123

Target: Calcium Channel

Cat.No: T13219

Target: Calcium Channel

Fostemsavir Tris

Cat.No: T10570

Synonym: BMS-663068 Tris

Target: HIV Protease

Cat.No: T9906

Target: Others

Cat.No: T0267

Synonym: AD 810,唑尼沙胺,CI 912

Target: Calcium Channel, Sodium Channel, Carbonic Anhydrase

Cat.No: TQ0153

Synonym: 米贝地尔,Ro 40-5967

Target: Calcium Channel

Cat.No: T71202

Cat.No: T33891

Synonym: PBI1393,BCH1393,BCH 1393,BCH-1393,PBI 1393

Cat.No: T62402

Cat.No: T80496

Target: Calcium Channel

Cat.No: T13220

Target: Others

Cat.No: T25874

Synonym: NMP7,NMP 7

Cat.No: T24738

ML218 hydrochloride

Cat.No: T12076

Target: Others

Cat.No: T69809

ABT-639 hydrochloride

Cat.No: T63312

Cat.No: T61393

Cat.No: T14120

Target: Others

Cat.No: T60648

Cav 3.2 inhibitor 3

Cat.No: T63350

Huwentoxin XVI TFA

Cat.No: T75792

NY-ESO-1 (87-111)

Cat.No: T40590

Cat.No: T37966

Cat.No: T62876

Cat.No: T26968

Synonym: CCT 036477,CCT-036477

Cintirorgon sodium

Cat.No: TQ0007L

Synonym: LYC-55716 sodium salt,LYC 55716,LYC55716

Cat.No: T11730

Target: Others

Cat.No: T81697

Cav 3.2 inhibitor 2

Cat.No: T63606

Cat.No: T29033

Synonym: 2-Aminooxyacetic acid,U 7524,Aminooxyacetic acid,U7524,AOAA

Cat.No: T61747

Cat.No: T78291

Synonym: BT-061

C12 Galactosylceramide (d18:1/12:0)

Cat.No: T36858

Cat. No.	Product Name	Target	Signaling Pathways
T10024	1-Octanol Octanol,正辛醇	Calcium Channel; Endogenous Metabolite	Membrane transporter/Ion channel; Metabolism
	1-Octanol (Octanol) 是一种饱和脂肪醇，是一种 T 型钙通道抑制剂，对天然 T 电流的IC50为 4 μM。它是一种具有类似柴油特性的极具吸引力的生物燃料。
T8716	physalin F 酸浆苦味素F,酸浆苦素 F	Apoptosis	Apoptosis
	Physalin F 是一种分泌型甾体，诱导人外周血单个核细胞凋亡，降低人 T 淋巴细胞 1 型病毒感染后的自发增殖和细胞因子的产生，具有强烈抗炎和免疫调节作用。
T0728	Ethosuximide Zarontin,乙琥胺	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Ethosuximide (Zarontin) 是一种抗癫痫药物，可改善多种神经退行性疾病模型的表型，且阻断低电压激活的 T 型钙通道。
T6S1885	Benzoylmesaconine Mesaconine 14-benzoate,苯甲酰新乌头原碱	Others	Others
	Benzoylmesaconine (Mesaconine 14-benzoate) 是乌头汤最丰富的组分。其中乌头汤可用于研究类风湿性关节炎。
T2S1792	Lycobetaine 石蒜内胺,Ungeremine,石蒜醋胺,石蒜碱内铵盐	Antibacterial	Microbiology/Virology
	Lycobetaine (Ungeremine) 是一种潜在的抗罗克福尔青霉和黑曲霉的生物杀菌剂。它对柱状黄杆菌有很强的抗菌活性。它有效地靶向哺乳动物以及细菌I 型和II 型拓扑异构酶。它显示出强烈的乙酰胆碱酯酶抑制活性（IC(50) 值为 0.35 microM）。它具有抗原生动物活性，在体外试验中对Trypanosoma brucei rhodesiense、T. cruzi 表现出良好的活性。
TN4587	Mulberrofuran C	HSV	Microbiology/Virology
	Mulberrofuran C shows protective effects on t-BHP-induced oxidative stress with the EC50 value of 0.41 ± 0.48 uM ; it also shows protective effects on glutamate-induced cell death with the EC50 value of 16.50 ± 7.82 uM. Mulberrofuran C has antiviral effects against herpes simplex virus type 1 and 2 (HSV-1 and HSV-2).
T73073	PTP1B-IN-21
	PTP1B-IN-21 是蛋白酪氨酸磷酸酶 1B (PTP1B) 的选择性抑制剂 (IC50=1.56 μM)，抑制力超出高度同源 T 细胞蛋白酪氨酸磷酸酶 (TCPTP；IC50>100 μM)，PTP1B 是抑制 2 型糖尿病的重要靶点。
T73072	PTP1B-IN-20
	PTP1B-IN-20 是蛋白酪氨酸磷酸酶 1B (PTP1B) 的选择性抑制剂 (IC50=1.05 μM)，抑制力超出高度同源 T 细胞蛋白酪氨酸磷酸酶 (TCPTP；IC50=78.0 μM)，PTP1B 是抑制 2 型糖尿病的重要靶点。
T36845	Isogarcinol
	Isogarcinol is a natural polyisoprenylated benzophenone first isolated from plant species in the genus Garcinia. It has immunosuppressant actions, inhibiting the protein phosphatase calcineurin (IC50 = 36 μM) and suppressing the proliferation of T cells. Oral administration of isogarcinol in mice decreases delayed type hypersensitivity, prolongs graft survival in allogeneic skin transplants, suppresses inflammation in collagen-induced arthritis, and reduces clinical symptoms in experimental auto...
T83864	Plipastatin A1 SNA-60-367-3,Fengycin IX
	Plipastatin A1是一种在B. cereus中发现的脂肽类化合物，具有酶抑制活性和免疫抑制活性。它能抑制磷脂酶A2（PLA2）、PLC和PLD（IC50分别为2.9、1.3和1.4 µM）。Plipastatin A1（100 µg/ml）能抑制LPS诱导的B细胞爆发生成和Concanavalin A诱导的T细胞爆发生成。在体内，Plipastatin A1（0.1 mg/动物）能抑制小鼠的迟发型超敏反应。
T35577	Phosphatidylserines (bovine)
	Phosphatidylserine is a naturally occurring phospholipid that comprises 2-10% of total phospholipids in mammals and is enriched in the central nervous system, particularly the retina. It is anionic and found mainly on the inner leaflet of the cell membrane. It is biosynthesized from phosphatidylcholine or phosphatidylethanolamine by phosphatidyl synthase 1 (PSS1) or PSS2, respectively, in the endoplasmic reticulum and can be reversibly converted back by the same enzymes. It can also be irreversi...
T37452	Stephacidin B
	Stephacidin B is a fungal metabolite that has been found inA. ochraceus.1Dimeric stephacidin B is rapidly converted to a monomer, avrainvillamide ,in vitro.2Stephacidin B is cytotoxic to a variety of cancer cells, including testosterone-independent PC3 and -sensitive LNCaP prostate cancer cells (IC50s = 0.37 and 0.06 μM, respectively) and estradiol-independent SK-BR-3 and -sensitive MCF-7 breast cancer cells (IC50s = 0.32 and 0.27 μM, respectively).1It induces apoptosis in HepG2 and Huh7 hepatoc...
T35779	Oosporein
	Oosporein is a mycotoxin that has been found inBeauveriaand has diverse biological activities.1,2It is cytotoxic to Sf9 and Sf21 insect cells with 50% cytotoxic concentration (CC50) values of 4.23 and 10.43 μM, respectively.3Oosporin induces lethality in day-old cockerels (LD50= 6.12 mg/kg).4It inhibits Na+/K+-, Ca2+-, and Mg2+-ATPase activities by 27, 52, and 100%, respectively, in equine erythrocyte ghosts when used at a concentration of 200 μg/ml.2Oosporein inhibits herpes simplex 1 (HSV-1), ...

天然产物

Cat.No: T10024

Synonym: Octanol,正辛醇

Target: Calcium Channel, Endogenous Metabolite

Cat.No: T8716

Synonym: 酸浆苦味素F,酸浆苦素 F

Target: Apoptosis

Cat.No: T0728

Synonym: Zarontin,乙琥胺

Target: Calcium Channel

Benzoylmesaconine

Cat.No: T6S1885

Synonym: Mesaconine 14-benzoate,苯甲酰新乌头原碱

Target: Others

Cat.No: T2S1792

Synonym: 石蒜内胺,Ungeremine,石蒜醋胺,石蒜碱内铵盐

Target: Antibacterial

Mulberrofuran C

Cat.No: TN4587

Target: HSV

Cat.No: T73073

Cat.No: T73072

Cat.No: T36845

Cat.No: T83864

Synonym: SNA-60-367-3,Fengycin IX

Phosphatidylserines (bovine)

Cat.No: T35577

Cat.No: T37452

Cat.No: T35779

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