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23

抑制剂 & 化合物

2

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T38286	C26 Sphingomyelin (d18:1/26:0) C26 Sphingomyelin (d18:1/26:0)
	C26 Sphingomyelin is a sphingolipid that has been found in serum and cell or brain extracts.1,2,3C26 sphingomyelin levels are increased in the serum of patients with hemophagocytic lymphohistiocytosis, an inflammatory condition characterized by excessive immune activation.3C26 sphingomyelin has been used a component of monolayers to study the influence of sphingomyelin acyl chain length on sphingomyelin-sterol interactions.4[Matreya, LLC.] 1.Wang, J.-R., Zhang, H., Yau, L.D., et al.Improved sphi...
T1520	Aliskiren hemifumarate 阿利克仑半富马酸盐,CGP 60536,SPP 100,CGP60536B	RAAS; Autophagy	Autophagy; Endocrinology/Hormones
	Aliskiren hemifumarate (CGP60536B) 一种可口服非肽肾素抑制剂，IC50为1.5 nM，具有抗高血压活性。
T69333	LX-5
	LX-5 is a selective activator of the p38 mitogen-activated protein kinase (MAPK) pathway. LX-5 de-represses a subset of endogenous genes repressed by DNA methylation.
T29541	AC265347 AC-265347	CaSR	GPCR/G Protein
	AC265347 是一种有效的钙敏感受体 (CaSR) 激动剂和 ago-PAM 正变构调节剂，具有抗肿瘤活性，通过诱导分化抑制神经母细胞瘤肿瘤生长。AC265347 可用于研究神经母细胞瘤。
T7127	DC260126	Apoptosis; GPR	Apoptosis; Endocrinology/Hormones; GPCR/G Protein
	DC260126 是一种 GPR40 (FFAR1)拮抗剂，对棕榈酸酯诱导的内质网应激和凋亡有保护作用。它剂量依赖性地抑制亚油酸、油酸、棕榈油酸和月桂酸刺激的 GPR40 介导的 Ca2+升高，IC50分别 6.28、5.96、7.07和4.58 μM。
T72054	SLC26A3-IN-1	transporter	Metabolism
	SLC26A3-IN-1 是一种阴离子交换蛋白 SLC26A3 的抑制剂，IC50值为340 nM。SLC26A3 属于溶质载体 (SLC) 蛋白，是 SLC26 家族成员之一。SLC26 家族对氯化物、碳酸氢盐、硫酸盐和草酸盐具有广泛的阴离子特异性。SLC26A3 在腺瘤 (DRA) 中下调，参与氯化物和草酸盐的肠道吸收且与氯离子丢失性腹泻有关。
T2440	IC261 SU-5607	Apoptosis; Casein Kinase; CDK	Apoptosis; Cell Cycle/Checkpoint; Metabolism; Stem Cells
	IC261 (SU-5607) 是一种选择性的，ATP 竞争性的CK1抑制剂，可触发有丝分裂检查点控制。对Ckiδ、Ckiε、 Ckiα1 和Cdk5的IC50值分别为 1 μM、1 μM 、16 μM 和4.5mM。
T11141	E64FC26	Others	Others
	E64FC26 是一种有效的蛋白质二硫键异构酶 (PDI) 家族泛抑制剂，具有抗肿瘤活性，抑制 PDIA1、PDIA3、PDIA4、TXNDC5 和 PDIA6，可用于研究多发性骨髓瘤和胰腺癌。
T74815	SLC26A3-IN-2
	SLC26A3-IN-2 是一种口服有效的阴离子交换蛋白 SLC26A3的抑制剂 (IC50=360 nM)。SLC26A3 属于溶质载体 (SLC) 蛋白，属于 SLC26 家族。SLC26 家族对氯化物、碳酸氢盐、硫酸盐和草酸盐具有广泛的阴离子特异性。SLC26A3 在腺瘤 (DRA) 中下调，参与氯化物和草酸盐的肠道吸收。SLC26A3 功能突变的丧失与氯离子丢失性腹泻有关。
T39812	(E/Z)-E64FC26 (E/Z)-E64FC26
	(E/Z)-E64FC26 is a mixture complex comprising E-E64FC26 and Z-E64FC26. E-E64FC26 is a highly potent pan-inhibitor of the protein disulfide isomerase (PDI) family, with IC50 values of 1.9, 20.9, 25.9, 16.3, and 25.4 μM against PDIA1, PDIA3, PDIA4, TXNDC5, and PDIA6, respectively. Furthermore, E64FC26 demonstrates anti-myeloma activity.
T39757	EC2629 EC2629
	EC2629 is a highly potent folate- receptor-targeted DNA crosslinking agent.
T78604	SLC26A3-IN-3
	SLC26A3-IN-3（化合物4az）是一种针对SLC26A3的抑制剂，IC50值为40 nM。该化合物主要应用于便秘和囊性纤维化的研究领域。
T33753	NSC265473 NSC-265473,NSC-305458,NSC305458,NSC 265473,NSC 305458
	NSC265473 is an ABCG2 substrate.
T60942	MC2652
	MC2652 (compound 1a) 是 LSD1的有效抑制剂，在白血病细胞 MV4-11 和 NB4 中表现出高抑制作用。MC2652 对前列腺癌的 LNCaP 细胞表现出抗增殖活性。
T14092	AC260584	Others	Others
	AC260584 is an M1 muscarinic receptor allosteric agonist (pEC50: 7.6).
T71190	FLC26
	FLC26 is a CK2 inhibitor with IC50 = 9 nM
T78579	NSC260594
	NSC260594是一种化合物，具有诱导细胞凋亡（Apoptosis）的作用。它通过与Mcl-1蛋白的浅沟结合并下调Wnt信号蛋白，抑制Mcl-1的表达。此外，NSC260594能够识别HIV的G9-G10-A11-G12 RNA四环，防止5'-UTR中的Gag蛋白结合。它被认为对抑制肿瘤生长具有潜在作用，特别是在三阴性乳腺癌（TNBC）研究中。
T35874	CC260
	CC260 is a selective PI5P4Kα and PI5P4Kβ inhibitor with Kis of 40 nM and 30 nM, respectively. CC260 does not inhibit or weakly inhibits other protein kinases, such as Plk1 and RSK2. CC260 can be used for cell energy metabolism, diabetes and cancer research[1]. In cultured C2C12 myotubes, CC260 (20 μM) enhances Insulin-induced Akt phosphorylation at both Thr-308 and Ser-473 but suppresses S6K phosphorylation (Thr-389) by mTORC1[1]. CC260 (2.5 μM, 5 μM, 10 μM, 20 μM) significantly increases phosph...
T60627	ELOVL1-IN-2	Others	Others
	ELOVL1-IN-2 是一种被称为极长链脂肪酸 1 (ELOVL1) 酶延长抑制剂的化合物，对 ELOVL1 表现出微弱的抑制作用（IC50 为 21 μM），并在原代细胞中表现出中等效力。对 HEK293 C26 细胞进行测定（IC50 为 6.7 μM）[1]。
T20050	Cinnamamide NSC 32953
	Cinnamamide is an amide of trans-cinnamic acid and a metabolite of Streptomyces. It also reduced tumor weight in a mouse model of C26 murine colon carcinoma, in vivo.
T61229	VEGFR-2/DHFR-IN-2
	VEGFR-2/DHFR-IN-2 (compound 5b) is a dual inhibitor targeting VEGFR-2 and DHFR, with respective IC50 values of 0.623 μM and 9.085 μM. It demonstrates potent cytotoxicity against C26, HepG2, and MCF7 cancer cell lines, with IC50 values ranging from 3.59 μM to 8.38 μM. VEGFR-2/DHFR-IN-2 holds promise for cancer research [1].
T38278	9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic Acid
	9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic acid is an ω-3 very long-chain polyunsaturated fatty acid. It has been used to study the desaturation and elongation of ω-3 polyunsaturated fatty acids. It is elongated to form C26:5 or acted on by δ6 desaturase to form C24:6. 9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic acid is found at low levels in mouse brain and spleen and levels decrease in the brain and spleen of old and exceptionally old mice.
T61489	VEGFR-2/DHFR-IN-1
	VEGFR-2/DHFR-IN-1 (compound 8b) 是 VEGFR-2和DHFR 的抑制剂，其IC50值分别为 0.384 和 7.881 μM。VEGFR-2/DHFR-IN-1 对大肠埃希菌，粪链球菌，肠沙门氏菌，金黄色酿脓葡萄球菌，MSSA 和MRSA 显示了良好的抗菌活性，MIC 值分别为 16，16，16，8 和 16 μg/mL。VEGFR-2/DHFR-IN-1 对 C26，HepG2 和 CF7 癌细胞系具有良好的细胞毒性，IC50值为 2.97-7.12 μM。VEGFR-2/DHFR-IN-1 可用于癌症的研究。

化合物

C26 Sphingomyelin (d18:1/26:0)

Cat.No: T38286

Synonym: C26 Sphingomyelin (d18:1/26:0)

Aliskiren hemifumarate

Cat.No: T1520

Synonym: 阿利克仑半富马酸盐,CGP 60536,SPP 100,CGP60536B

Target: RAAS, Autophagy

Cat.No: T69333

Cat.No: T29541

Synonym: AC-265347

Target: CaSR

Cat.No: T7127

Target: Apoptosis, GPR

Cat.No: T72054

Target: transporter

Cat.No: T2440

Synonym: SU-5607

Target: Apoptosis, Casein Kinase, CDK

Cat.No: T11141

Target: Others

Cat.No: T74815

Cat.No: T39812

Synonym: (E/Z)-E64FC26

Cat.No: T39757

Synonym: EC2629

Cat.No: T78604

Cat.No: T33753

Synonym: NSC-265473,NSC-305458,NSC305458,NSC 265473,NSC 305458

Cat.No: T60942

Cat.No: T14092

Target: Others

Cat.No: T71190

Cat.No: T78579

Cat.No: T35874

Cat.No: T60627

Target: Others

Cat.No: T20050

Synonym: NSC 32953

VEGFR-2/DHFR-IN-2

Cat.No: T61229

9(Z),12(Z),15(Z),18(Z),21(Z)-Tetracosapentaenoic Acid

Cat.No: T38278

VEGFR-2/DHFR-IN-1

Cat.No: T61489

Cat. No.	Product Name	Target	Signaling Pathways
T3844	Deltonin 三角叶薯蓣皂苷	ERK; Others; Akt; Endogenous Metabolite	Cytoskeletal Signaling; MAPK; Metabolism; Others; PI3K/Akt/mTOR signaling
	Deltonin 是从盾叶薯蓣中得到的一种甾体皂苷，抑制ERK1/2和AKT 的活化，具有抗肿瘤活性。
T13501	3-Oxo-21α-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone 3-oxo-21-alpha-methoxy-24-25-26-27-tetranortirucall-7-ene-23-21-lactone	Others	Others
	The compound 3-Oxo-21α-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone is a cytotoxic tirucallane C26 triterpenoid that has been extracted from the stem barks of Aphanamixis grandifolia.

天然产物

Cat.No: T3844

Synonym: 三角叶薯蓣皂苷

Target: ERK, Others, Akt, Endogenous Metabolite

3-Oxo-21α-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone

Cat.No: T13501

Synonym: 3-oxo-21-alpha-methoxy-24-25-26-27-tetranortirucall-7-ene-23-21-lactone

Target: Others

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