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Search Results for " f1 "

117

抑制剂 & 化合物

14

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T19840	GSK-F1 PI4KA inhibitor-F1	PI4K	PI3K/Akt/mTOR signaling
	GSK-F1 (PI4KA inhibitor-F1) 是一种新型强效 PI4KA 抑制剂。
T67837	(3S)-GSK-F1 PI4KA inhibitor-F1	PI4K	PI3K/Akt/mTOR signaling
	(3S)-GSK-F1是一种选择性PI4KIIIα抑制剂，pIC50=8.3。
T83670	F1 TFA Tat-IKIP (46-60),Tat-Inhibitor of NF-κB Kinase-interacting Peptide
	F1是一种抗炎肽，由HIV-1 Tat蛋白质转导域与对应于抑制因子NF-κB激酶-相互作用肽（IKIP）46-60残基的15氨基酸肽链接而成。在5 µM浓度下，F1抑制了小鼠腹腔巨噬细胞中LPS诱导的IκB激酶α（IKKα）和IKKβ的磷酸化以及NF-κB（p65）的核内转移。在体内，F1（5 mg/kg）降低了LPS诱导的脓毒症小鼠模型中IL-6、TNF-α和IL-1β的血清水平，并增加了生存率。
T126048	Coreanoside F1
	Coreanoside F1 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T126048，CAS号为 132282-69-0。
T125155	Schidigerasaponin F1
	Schidigerasaponin F1 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T125155，CAS号为 266998-42-9。
TP2476	Tnrnflrfamide Thr-asn-arg-asn-phe-leu-arg-phe-NH2,Peptide F(1), lobster,F1 Peptide, lobster,Lobster peptide F1
	Tnrnflrfamide is a SCP (small cardioactive peptide)-like peptide found in lobster neurons; exhibits FMRFamide-like immunoreactivity.
T11254	F-1	ROS; ALK; ROS Kinase	Angiogenesis; Immunology/Inflammation; Tyrosine Kinase/Adaptors
	F-1 是 ALK 和 ROS1 的双重抑制剂，抑制 ALK 的磷酸化及下游通路，可作用于对 ALKWT (IC50:2.1 nM)，ROS1WT (IC50:2.3 nM)，ALKL1196M (IC50:1.3 nM) 和 ALKG1202R (IC50:3.9 nM)。
T37919	Prostaglandin F1α PGF1α,Prostaglandin F1α
	Prostaglandin F1α (PGF1α) is the putative metabolite of dihomo-γ-linolenic acid (DGLA) via the cyclooxygenase (COX) pathway. Both PGF1α and PGF2α have been shown to act as priming pheromones for male Atlantic salmon with a threshold concentration of 10-11 M. [1] PGF1α binds to the ovine corpus luteum FP receptor at only 8% of the relative potency of PGF2α. [2] It is only half as active as PGF2α in inducing human respiratory smooth muscle contractions in vitro. [3]
T36162	8-iso Prostaglandin F1α 8-iso Prostaglandin F1α
	8-iso PGF1α is an isoprostane that was first identified in human semen. It is a member of the isoprostane family, which are eicosanoids of non-cyclooxygenase origin. 8-iso PGF1α is present along with its 19-hydroxy congener at 5-10 μg/ml of seminal plasma.
T36163	8-iso Prostaglandin F1β 8-iso Prostaglandin F1β
	8-iso PGF1β is a potential autoxidation product of DGLA. There are no published reports on its isolation from any biological source or on its biological activity.
T36772	11-deoxy Prostaglandin F1β 11-deoxy Prostaglandin F1β
	11-deoxy PGF1β is a synthetic analog of PGF1β. In contrast to PGF2α and PGF1α, 11-deoxy PGF1β exhibits vasodepressor and bronchodilator activities in guinea pigs at a dose of 500 μg/kg.
T37990	15-keto Prostaglandin F1α 15-keto Prostaglandin F1α
	15-keto PGF1α is the initial metabolite of PGF1α via 15-hydroxy PGDH. In mammals, oxidation of C-15 markedly attenuates receptor binding and activity. In fish, the 15-keto compounds serve as post-ovulatory pheromones and are more active than the parent prostaglandins.
T36771	11-deoxy Prostaglandin F1α 11-deoxy Prostaglandin F1α
	11-deoxy PGF1α is a synthetic analog of PGF1α. In whole animal studies, a dose of 32 mg/kg inhibited gastric acid secretion by 35%. 11-deoxy PGF1α is also known to cause rat uterine contractions at a dose 0.3 times that of PGF1α. It also exhibits vasopressor and bronchoconstrictor activities at about half the potency of PGF2α in guinea pigs.
T36148	13,14-dihydro-15-keto Prostaglandin F1α 13,14-dihydro-15-keto Prostaglandin F1α
	13,14-dihydro-15-keto Prostaglandin F1α (13,14-dihydro-15-keto PGF1α) is a metabolite of PGF1α that has been reported in the rat stomach. The measurement of 13,14-dihydro-15-keto PGF1α can be used as a marker of the in vivo production of PGF1α.
T36724	6,15-diketo-13,14-dihydro Prostaglandin F1α 6,15-diketo-13,14-dihydro Prostaglandin F1α
	6,15-diketo-13,14-dihydro PGF1α is a metabolite of PGI2. It was shown to enhance intracellular cAMP and cholesterol catabolism in bovine arterial smooth muscle cells.
T83662	2,3-dinor-8-iso Prostaglandin F1α 2,3-dinor-8-iso PGF1α,2,3-dinor-iPF1α-III,2,3-dinor-5,6-dihydro-15-F2t-Isoprostane,2,3-dinor-5,6-dihydro-15-F2t-IsoP
	2,3-dinor-8-iso Prostaglandin F1α（2,3-dinor-8-iso PGF1α）是一种异前列腺素和花生四烯酸的活性代谢物，也是血小板聚集抑制剂8-iso PGF2α的产物。它通过花生四烯酸的非酶促自由基过氧化作用形成。2,3-dinor-8-iso PGF1α在孤立的猪视网膜和大脑微血管中引起血管收缩（EC50s分别为12.8和18.5 nM），但在31 µM的浓度下使用时不会引起孤立的大鼠主动脉环的收缩。在1 µM的浓度下使用时，它能增加孤立的猪大脑切片中的血栓素B2（TXB2）水平，这一效应可以通过血栓素A合成酶抑制剂CGS 12970、电压门控钙通道抑制剂SKF 96365或烟碱型乙酰胆碱受体（nAChR）拮抗剂α-conotoxin来逆转。
T13194	CSF1R-IN-2	c-Fms; c-Met/HGFR; Src	Angiogenesis; Tyrosine Kinase/Adaptors
	CSF1R-IN-2 是一种口服具有活力的、有效的 SRC，MET 和 c-FMS 抑制剂，它们的 IC50 值分别为 0.12 nM，0.14 nM 和 0.76 nM。
T77745	N6F11	GPX	oxidation-reduction
	N6F11是一种新型且具有选择性和有效性的铁死亡诱导剂，具有抗癌抗肿瘤活性，通过与癌细胞中的TRIM25结合从而促进GPX4降解。N6F11 可用于研究胰腺癌。
T10894	CSF1R-IN-1	c-Fms	Tyrosine Kinase/Adaptors
	CSF1R-IN-1 是一种 CSF1R 抑制剂 (IC50:0.5 nM)。
T64066	CSF1R-IN-3	c-Fms; CSF-1R	Tyrosine Kinase/Adaptors
	CSF1R-IN-3是一种口服有效的 CSF-1R 抑制剂，IC50值为2.1nM。CSF1R-IN-3对结直肠癌细胞具有抗增殖活性。CSF1R-IN-3 通过抑制巨噬细胞的迁移，诱导 M2 型巨噬细胞重新编程为 M1 型巨噬细胞，从而表现出抗肿瘤作用和提高免疫力的作用，展现对结直肠癌细胞的活性。
T13324	VUF11207 fumarate	CXCR; Arrestin	Autophagy; GPCR/G Protein; Immunology/Inflammation
	VUF11207 fumarate 是一种 CXCR7激动剂和高效CXCR7配体，pKi 为 8.1。它可诱导CXCR7的β-arrestin2募集和随后的内在化，pEC50分别为 8.8 和 7.9。
T77767L1	GLF16 HCl	Others	Others
	GLF16 HCl 是一种荧光团偶联的苏丹黑 B 类似物，可通过通过荧光显微镜和流式细胞术快速检测、分离和实时跟踪衰老细胞。
T61112	SLF1081851	LPL Receptor	GPCR/G Protein
	SLF1081851 是一种 Spns2 抑制剂，抑制 S1P 释放 (IC50=1.93 μM)。SLF1081851 在发育和免疫系统中起关键作用。
T6667	SF1670 PTP CD45 Inhibitor,PTPase CD45 Inhibitor	Phosphatase; PTEN; Autophagy	Autophagy; Metabolism; PI3K/Akt/mTOR signaling
	SF1670 (PTPase CD45 Inhibitor) 是一种特异性 PTEN 抑制剂，IC50 为 2 μM。
T15266	F16 (E)-4-(3-indolylvinyl)-N-methylpyridinium iodide	Others	Others
	F16 ((E)-4-(3-indolylvinyl)-N-methylpyridinium iodide)抑制neu-overeigning 细胞的生长和乳腺上皮的增殖。
T60026	KIF18A-IN-2	Microtubule Associated	Cytoskeletal Signaling
	KIF18A-IN-2 是有丝分裂驱动蛋白 Kif18A 的抑制剂，IC50 为 28 nM，可用于染色体不稳定性相关漏洞的研究。
T4308	F1063-0967	Phosphatase	Metabolism
	F1063-0967 是双特异性磷酸酶 26 抑制剂，其IC50=11.62 μM。
T16904	Smurf1-IN-A01 A01	Others	Others
	Smurf1-IN-A01 (A01) 是泛素连接酶 Smad 泛素化调节因子-1(Smurf1)抑制剂，其kd=3.664 nM。它能够抑制 Smurf1 介导的 Smad1/5 降解，并提高 BMP-2 的反应性。
T22774L	eukaryotic translation elongation factor 1 alpha 1 (EEF1A1) (387-394) [Multiple species]（TFA)	Others	Others
	eukaryotic translation elongation factor 1 alpha 1 (EEF1A1) (387-394) [Multiple species](TFA) 是延伸因子 1 亚基。真核翻译延伸因子 1 alpha 1 (EEF1A1) 编码延伸因子 alpha 亚基的同种型- 1 复合物，负责将氨酰 tRNA 酶促递送至核糖体。这种亚型（α 1）在脑、胎盘、肺、肝、肾和胰腺中表达，另一种亚型（α 2）在脑、心脏和骨骼肌中表达。这种亚型在 66% 的 Felty 综合征患者中被鉴定为自身抗原。已发现该基因在许多染色体上具有多个拷贝，其中一些（如果不是全部）代表不同的假基因。
T12125	MuRF1-IN-1	Others	Others
	MuRF1-IN-1 是MuRF1抑制剂，能减少心脏恶病质中的骨骼肌萎缩和功能障碍。
T15409	GNF179	Parasite	Microbiology/Virology
	GNF179 是8,8-二甲基 IP 类似物。它表现出对多药耐药菌株 W2 的效力，具有良好的体外代谢稳定性和体内口服生物相容性。
T9890	HIF1-IN-3 Benzenepropanamide, N-[(8-hydroxy-7-quinolinyl)(4-methoxyphenyl)methyl]-	HIF	Angiogenesis; Chromatin/Epigenetic
	HIF1-IN-3 (Benzenepropanamide, N-[(8-hydroxy-7-quinolinyl)(4-methoxyphenyl)methyl]-) 是HIF-1的有效抑制剂（EC50 = 0.9 μM）,可用于抗癌的研究。
T4125	HSF1A	HSP	Cytoskeletal Signaling; Metabolism
	HSF1A 是一种可渗透细胞的 HSF1 激活剂，可保护哺乳动物细胞免受应激诱导的细胞凋亡。它还是 TRiC/CCT 的特异性抑制剂。
T3963	VUF10460	Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	VUF10460 是一种非咪唑组胺 H4 受体激动剂，与大鼠H4受体结合的pKi 值为7.46。
T24949	VUF10132 VUF-10132,VUF 10132
	VUF10132 is a full inverse CXCR3 N3.35A agonist.
T40232	KIF18A-IN-1 KIF18A-IN-1
	KIF18A-IN-1 is a potent inhibitor of the mitotic kinesin KIF18A. This compound demonstrates significant anti-tumor properties.
T26785	BFF122 BFF 122,BF5,BFF-122
	BFF122 is an inhibitor of kynurenine aminotransferase II (KAT II).
T70872	Smurf1 inhibitor 1
	Smurf1 inhibitor 1 is a inhibitor that promotes bone formation.
T62318	CSF1R-IN-9
	CSF1R-IN-9 (Compound 46) 是一种 CSF-1R 抑制剂 (IC50: 0.028 μM)。
T74271	TRIM24/BRPF1-IN-2
	TRIM24/BRPF1-IN-2 (compound 20l) 是一种有效的 TRIM24/BRPF1双重抑制剂，IC50值分别为 0.98 和 1.16 μM。 TRIM24/BRPF1-IN-2 显示出 TRIM24/BRPF1 溴结构域结合亲和力。 TRIM24/BRPF1-IN-2 可用于前列腺癌研究。
TP1268	CEF19, Epstein-Barr Virus latent NA-3A (458-466) CEF19,Epstein-Barr Virus latent NA-3A 458-466
	CEF19, Epstein-Barr Virus latent NA-3A (458-466) is a single peptide epitope, YPLHEQHGM, representing residues 458-466 of the type 1 Epstein-Barr Virus (EBV) nuclear antigen 3A protein (B95.8 strain).
T15661	Kif15-IN-1	Others	Others
	Kif15-IN-1, a mitotic Kinesin family member 15 (Kif15) inhibitor, is utilized in the study of cellular proliferative diseases.
TP2402	Peptide VF13N Epitope VF13N
	Peptide VF13N is a synthetic rabies virus glycoprotein T helper cell epitope.
T77932	PF15 TFA	PROTACs	PROTAC
	PF15 TFA是一种连接FLT3 kinase配体和CRBN配体的PROTAC，作为FLT3-ITD的高选择性降解剂，DC50值为76.7 nM。该化合物可显著抑制FLT3-ITD阳性细胞增殖，并降低FLT3和STAT5磷酸化水平。PF15 TFA亦能抑制小鼠模型的肿瘤生长，并可用于白血病研究。
T70403	VUF14480
	VUF14480 is a covalent partial agonist that interacts with cysteine 98(3.36) of the human histamine H₄ receptor. VUF14480 was shown to be a partial agonist of hH4 receptor-mediated G protein signalling and β-arrestin2 recruitment. VUF14480 bound covalently to the hH₄ receptor with submicromolar affinity. Serine substitution of C98(3.36) prevented this covalent interaction.
T62364	CSF1R-IN-5
	CSF1R-IN-5 是一种 CSF1R 的有效抑制剂。其中 CSF-1R 表达于巨噬细胞中，巨噬细胞的存活和分化依赖于 CSF-1/CSF-1R 信号通路。CSF1R-IN-5 可以影响 TAM 和胶质瘤细胞之间炎症因子的交换。CSF1R-IN-5 具有潜力进行癌症疾病的研究。
T74336	YF135
	YF135为一种效能高的KRASG12CPROTAC，能可逆地促使共价结合。该化合物采用KRAS G12C inhibitor 48（compound 6d）作为配体，并以MRTX849搭配VHL配体作为框架进行设计与合成。通过E3连接酶VHL介导的蛋白酶体途径，YF135显著诱导KRASG12C的降解并可逆地降低ERK磷酸化水平。
T28790	SKF1
	SKF1 is a suppressor of the ability of FK506. SKF1 inhibits cell growth in the presence of high levels of NaCl, induces cell death in low salt conditions, interacts directly with yeast mitochodria.
T76245L	CKLF1-C27 TFA
	CKLF1-C27 是 CKLF1 的 C 末端肽，与 CCR4受体结合并激活 ERK1/2通路。CKLF1-C27 可以通过竞争 CCR4受体来消除 CKLF1 对细胞的影响。CKLF1-C27对促进 HUVECs 增殖有很大的作用。CKLF1-C27 具有用于银屑病研究的潜力。
T61554	CSF1R-IN-13
	CSF1R-IN-13 is a powerful CSF1R inhibitor with potential applications in researching cancer diseases [1]. CSF1R, also known as colony stimulating factor 1 receptor, is a critical growth factor that regulates various cell types, including bone marrow progenitor cells, monocytes, macrophages, and giants [1]. CSF1R-IN-13 shows promise in furthering our understanding of cancer-related disorders (WO2019134661A1, compound 32) [1].

化合物

Cat.No: T19840

Synonym: PI4KA inhibitor-F1

Target: PI4K

Cat.No: T67837

Synonym: PI4KA inhibitor-F1

Target: PI4K

Cat.No: T83670

Synonym: Tat-IKIP (46-60),Tat-Inhibitor of NF-κB Kinase-interacting Peptide

Cat.No: T126048

Schidigerasaponin F1

Cat.No: T125155

Cat.No: TP2476

Synonym: Thr-asn-arg-asn-phe-leu-arg-phe-NH2,Peptide F(1), lobster,F1 Peptide, lobster,Lobster peptide F1

Cat.No: T11254

Target: ROS, ALK, ROS Kinase

Prostaglandin F1α

Cat.No: T37919

Synonym: PGF1α,Prostaglandin F1α

8-iso Prostaglandin F1α

Cat.No: T36162

Synonym: 8-iso Prostaglandin F1α

8-iso Prostaglandin F1β

Cat.No: T36163

Synonym: 8-iso Prostaglandin F1β

11-deoxy Prostaglandin F1β

Cat.No: T36772

Synonym: 11-deoxy Prostaglandin F1β

15-keto Prostaglandin F1α

Cat.No: T37990

Synonym: 15-keto Prostaglandin F1α

11-deoxy Prostaglandin F1α

Cat.No: T36771

Synonym: 11-deoxy Prostaglandin F1α

13,14-dihydro-15-keto Prostaglandin F1α

Cat.No: T36148

Synonym: 13,14-dihydro-15-keto Prostaglandin F1α

6,15-diketo-13,14-dihydro Prostaglandin F1α

Cat.No: T36724

Synonym: 6,15-diketo-13,14-dihydro Prostaglandin F1α

2,3-dinor-8-iso Prostaglandin F1α

Cat.No: T83662

Synonym: 2,3-dinor-8-iso PGF1α,2,3-dinor-iPF1α-III,2,3-dinor-5,6-dihydro-15-F2t-Isoprostane,2,3-dinor-5,6-dihydro-15-F2t-IsoP

Cat.No: T13194

Target: c-Fms, c-Met/HGFR, Src

Cat.No: T77745

Target: GPX

Cat.No: T10894

Target: c-Fms

Cat.No: T64066

Target: c-Fms, CSF-1R

VUF11207 fumarate

Cat.No: T13324

Target: CXCR, Arrestin

Cat.No: T77767L1

Target: Others

Cat.No: T61112

Target: LPL Receptor

Cat.No: T6667

Synonym: PTP CD45 Inhibitor,PTPase CD45 Inhibitor

Target: Phosphatase, PTEN, Autophagy

Cat.No: T15266

Synonym: (E)-4-(3-indolylvinyl)-N-methylpyridinium iodide

Target: Others

Cat.No: T60026

Target: Microtubule Associated

Cat.No: T4308

Target: Phosphatase

Cat.No: T16904

Synonym: A01

Target: Others

eukaryotic translation elongation factor 1 alpha 1 (EEF1A1) (387-394) [Multiple species]（TFA)

Cat.No: T22774L

Target: Others

Cat.No: T12125

Target: Others

Cat.No: T15409

Target: Parasite

Cat.No: T9890

Synonym: Benzenepropanamide, N-[(8-hydroxy-7-quinolinyl)(4-methoxyphenyl)methyl]-

Target: HIF

Cat.No: T4125

Target: HSP

Cat.No: T3963

Target: Histamine Receptor

Cat.No: T24949

Synonym: VUF-10132,VUF 10132

Cat.No: T40232

Synonym: KIF18A-IN-1

Cat.No: T26785

Synonym: BFF 122,BF5,BFF-122

Smurf1 inhibitor 1

Cat.No: T70872

Cat.No: T62318

TRIM24/BRPF1-IN-2

Cat.No: T74271

CEF19, Epstein-Barr Virus latent NA-3A (458-466)

Cat.No: TP1268

Synonym: CEF19,Epstein-Barr Virus latent NA-3A 458-466

Cat.No: T15661

Target: Others

Cat.No: TP2402

Synonym: Epitope VF13N

Cat.No: T77932

Target: PROTACs

Cat.No: T70403

Cat.No: T62364

Cat.No: T74336

Cat.No: T28790

Cat.No: T76245L

Cat.No: T61554

Cat. No.	Product Name	Target	Signaling Pathways
T3401	Ginsenoside F1 人参皂苷 F1,20(S)-Ginsenoside F1	P450; Endogenous Metabolite	Metabolism
	Ginsenoside F1 (20(S)-Ginsenoside F1) 是一种 Ginsenoside Rg1 的酶促修饰衍生物，它竞争性抑制CYP3A4，对 CYP2D6 具有较弱的抑制作用。
TN1942	Momordicoside F1 苦瓜皂苷 F1	Others	Others
	Momordicoside F1 may have antiproliferative activities against MCF-7, WiDr, HEp-2, and Doay human tumor cell lines.
TN1989	Niga-ichigoside F1 苦莓苷F1	Others; Nrf2	Immunology/Inflammation; Others
	Niga-ichigoside F1(NI) has anti-inflammatory, gastroprotective ,antinociceptive, and cytotoxic effects.
TN4161	Goshonoside F1
	Goshonoside F1是半糯米品种水稻的脂质代谢产物，可被当作培育优良水稻的一个指标。
TN1080	Kaji-ichigoside F1 蔷薇苷
	Kaji-ichigoside F1 shows antiinflammatory/antinociceptive action in acetic acid-induced writhing and hot plate testing and in a carrageenan-induced paw edema model in mice and rats. Kaji-ichigoside F1 exhibits in vivo hepatoprotective effects, it inhibite
TN6448	3-Acetyl-ginsenoside F1
	3-Acetyl-ginsenoside F1 可用于生命科学领域的相关研究，其产品编号为 TN6448。
T81853	Marstenacisside F1
	Marstenacisside F1（化合物1）为从通关藤(Marsdenia tenacissima)分离的抗炎聚氧孕烷苷，能抑制脂多糖激活的RAW 264.7细胞产生一氧化氮(NO)，属Tenacigenin B衍生物。
TN2242	Suavissimoside R1 甜叶苷R1,Suavissimoside F1	Others	Others
	Suavissimoside F1 is a natural product
T3920	Pseudoginsenoside F11 Ginsenoside A1,拟人参皂苷 F11,拟人参皂苷F11	Others; Endogenous Metabolite	Metabolism; Others
	Pseudoginsenoside F11 (Ginsenoside A1) 从人参根和叶中分离得到。PF11在一系列心血管和中枢神经系统疾病中具有广泛的保护作用。
TN4049	F1839-I	Others	Others
	F1839-I is a natural product from Stachybotrys sp.
T19328	Fructo-oligosaccharide DP11/GF10	Others	Others
	Fructo-oligosaccharide DP11/GF10 is a fructooligosaccharide (FOS) compound with a degree of polymerization (DP) equal to 11. FOS consists of 10 fructose units connected by (2→1)-β-glycosidic bonds, with a single D-glucosyl unit present at the non-reducing end.
T19329	Fructo-oligosaccharide DP12/GF11 蔗果十二糖	Others	Others
	Fructo-oligosaccharide DP12/GF11 is a member of fructooligosaccharides (FOS) characterized by a degree of polymerization (DP) of 12. FOS compounds consist of 11 fructose units connected by (2→1)-β-glycosidic bonds, with a lone D-glucosyl unit located at the non-reducing end.
T3S0153	Xanthatin 苍耳亭,叶黄制菌素	Apoptosis; VEGFR; Lipoxygenase; Wnt/beta-catenin; Antibacterial	Angiogenesis; Apoptosis; Cytoskeletal Signaling; Metabolism; Microbiology/Virology; Stem Cells; Tyrosine Kinase/Adaptors
	Xanthatin 是一种从Xanthium strumarium 叶子中提取的天然产物，可诱导细胞凋亡。它抑制布鲁氏菌的IC50值为 2.63 μg/ mL，对寄生虫特异性锥虫硫磷还原酶具有不可逆的弱抑制作用。它通过抑制PGE2的合成和 5-脂氧合酶的活性而显示出抗炎活性。
T13123	Tentoxin	Endogenous Metabolite	Metabolism
	Tentoxin 是一种由植物致病真菌产生的环状肽，在敏感植物中，当其浓度在纳摩尔到微摩尔之间时，会使 F1马达失活，而更高的浓度会超过该酶的天然活性

天然产物

Cat.No: T3401

Synonym: 人参皂苷 F1,20(S)-Ginsenoside F1

Target: P450, Endogenous Metabolite

Momordicoside F1

Cat.No: TN1942

Synonym: 苦瓜皂苷 F1

Target: Others

Niga-ichigoside F1

Cat.No: TN1989

Synonym: 苦莓苷F1

Target: Others, Nrf2

Cat.No: TN4161

Kaji-ichigoside F1

Cat.No: TN1080

Synonym: 蔷薇苷

3-Acetyl-ginsenoside F1

Cat.No: TN6448

Marstenacisside F1

Cat.No: T81853

Suavissimoside R1

Cat.No: TN2242

Synonym: 甜叶苷R1,Suavissimoside F1

Target: Others

Pseudoginsenoside F11

Cat.No: T3920

Synonym: Ginsenoside A1,拟人参皂苷 F11,拟人参皂苷F11

Target: Others, Endogenous Metabolite

Cat.No: TN4049

Target: Others

Fructo-oligosaccharide DP11/GF10

Cat.No: T19328

Target: Others

Fructo-oligosaccharide DP12/GF11

Cat.No: T19329

Synonym: 蔗果十二糖

Target: Others

Cat.No: T3S0153

Synonym: 苍耳亭,叶黄制菌素

Target: Apoptosis, VEGFR, Lipoxygenase, Wnt/beta-catenin, Antibacterial

Cat.No: T13123

Target: Endogenous Metabolite

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