首页工具

登录

搜索结果

Search Results for " smc "

25

抑制剂 & 化合物

1

天然产物

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T7133	Anagliptin SK-0403,阿拉格列汀	Proteasome; DPP-4	Proteases/Proteasome; Ubiquitination
	Anagliptin (SK-0403) 是一种选择性的二肽酰肽酶 4 抑制剂，IC50=3.8 nM，对 DPP-8/9 的选择性相对较弱，IC50分别为 68 和 60 nM。
T11917	Lys-SMCC-DM1 Lys-Nε-MCC-DM1	Microtubule Associated	Cytoskeletal Signaling
	DM1 是一种微管蛋白抑制剂。 Lys-SMCC-DM1 (Lys-Nε-MCC-DM1) 是 DM1 的活性代谢物。
T16899	SMCC-DM1 DM1-SMCC	Others	Others
	SMCC-DM1 (DM1-SMCC) 是一种药物-接头偶联物，由有效的微管破坏剂 DM1 和接头 SMCC 组成，用于制备抗体药物偶联物。
T18728	Sulfo-SMCC sodium	Others	Others
	Sulfo-SMCC sodium 是一种异双功能、不可裂解的 ADC 交联剂，带有 N-羟基琥珀酰亚胺酯和马来酰亚胺基团，分别与伯胺和巯基反应。
T9116	SMCC N-Succinimidyl 4-(N-maleimidomethyl)cycl,4-(N-马来酰亚胺基甲基)环己烷-1-羧酸琥珀酰亚胺酯	Others	Others
	SMCC (N-Succinimidyl 4-(N-maleimidomethyl)cycl) 是一种异双功能蛋白质交联剂。它接合抗原耦合脾脏细胞来诱导抗原特异性免疫反应。
T28289	Paclitaxel-SMCC SMCC taxol, Taxol-SMCC, Taxol SMCC,Paclitaxel with SMCC linker,SMCC-Taxol,Paclitaxel ADC conjugate.
	Paclitaxel-SMCC is a paclitaxel derivative with a SMCC linker. (Succinimidyl-4-( N -maleimidomethyl)cyclohexane-1-carboxylate). Paclitaxel-SMCC can be used to synthesize Paclitaxel bioconjugates with enzymes, antobodies, antigens and other biopolymers. Pa
TP1639	Smcy HY Peptide (738-746) Smcy HY Peptide 738-746
	Smcy HY Peptide (738-746) is an H2-Db-restricted peptide, derived from the amino acid sequence 738 to 746 of the Smcy protein.
T18856	trans-Sulfo-SMCC	Others	Others
	trans-Sulfo-SMCC is a non-cleavable and membrane permeable ADC crosslinker.
T15161	Doxorubicin-SMCC	Others	Others
	Doxorubicin-SMCC is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
T63090	SMCypI C31
	SMCypIC31 是一种非肽类 cyclophilin 抑制剂，能够有效抑制肽基-脯氨酰顺/反异构酶 (PPIase) (IC50: 0.1 μM)。SMCypI C31 可以破坏亲环蛋白 A-NS5A 相互作用。SMCypI C31 具有泛基因型抗 HCV 效果，对基因型 1a，1b，2a，3a 和 5a HCV-SGRs 和嵌合基因型 2a/4a HCV-SGRs 的 EC50 范围为 1.20-7.76 μM。
T18361	MMAE-SMCC	Others	Others
	MMAE-SMCC is a drug-linker conjugate designed for antibody-drug conjugates (ADC). It consists of MMAE, a potent inhibitor of mitosis and tubulin, and SMCC, a linker that facilitates the development of ADCs.
T33865	Palbociclib-SMCC PD0332991-SMCC,Palbociclib-SMCC linker,PD 0332991-SMCC,PD-0332991-SMCC
	Palbociclib-SMCC is a Palbociclib derivative with a SMCC linker.
T17833	DM4-SMCC	Others	Others
	DM4-SMCC, a non-cleavable drug-linker conjugate for antibody-drug conjugates (ADC), leverages the antitumor efficacy of DM4 (an antitubulin agent) through attachment with the SMCC linker, exhibiting antitumor activity[1].
T81280	Rha-PEG3-SMCC
	Rha-PEG3-SMCC（compound 13）作为一种构成部分，集成了蛋白质交联剂SMCC与不可降解的ADC linker Rha-PEG3，用于抗体-活性分子偶联物的构建。
T72050	4-N-Dodecyloxyphenol 4-dodecoxyphenol,p-Dodecyloxyphenol
	4-N-Dodecyloxyphenol (p-Dodecyloxyphenol) 是一种可作为铁电液晶或铁电液晶的添加剂或显示SmC 相且无手性基团的化合物。
T6265	Bosentan (hydrate) 波生坦水合物,Bosentan Hydrate,Benzenesulfonamide,Actelion,Ro 47-0203	Endothelin Receptor	GPCR/G Protein
	Bosentan hydrate (Ro 47-0203) 是endothelin-1 (ET)竞争性拮抗剂，在人SMC 细胞中，它能够作用于 ETA 受体(Ki:4.7 nM)和 ETB 受体(Ki:95 nM)。
T3116	Atorvastatin hemicalcium salt Lipitor,Atorvastatin hemicalcium,Atorvastatin Calcium,CI-981,阿托伐他汀钙,Sortis	Ferroptosis; HMG-CoA Reductase; Autophagy	Apoptosis; Autophagy; Metabolism
	Atorvastatin hemicalcium salt (Atorvastatin Calcium) 是一种口服有效的 HMG-CoA 还原酶抑制剂，可用作降低胆固醇的药物。它抑制人 SV-SMC 增殖和侵袭，IC50分别为 0.39 μM 和 2.39 μM。
TP1016L	Aviptadil Acetate 醋酸阿肽地尔,阿肽地尔,Vasoactive Intestinal Peptide acetate salt	RAAS; SARS-CoV	Endocrinology/Hormones; Microbiology/Virology
	Aviptadil Acetate (Vasoactive Intestinal Peptide acetate salt) 是模拟血管活性肠多肽类似物，具有血管舒张效应。它可诱导肺血管舒张并抑制血管 SMC 的增殖和血小板聚集。它可用于研究 SARS-CoV-2 引起的肺纤维化、肺动脉高压和呼吸衰竭。
T6264	Bosentan Actelion,波生坦,Ro 47-0203,Benzenesulfonamide	Endothelin Receptor	GPCR/G Protein
	Bosentan (Benzenesulfonamide) 是 endothelin-1 (ET)拮抗剂，在人的 SMC 细胞中，它能够作用于 ETA 受体(Ki:4.7 nM)和 ETB 受体(Ki:95 nM)。
T72101	Atorvastatin hemicalcium trihydrate 阿托伐他汀半钙三水合物,阿托他伐汀半钙三水合物
	Atorvastatin hemicalcium trihydrate 是一种具有口服活性的 HMG-CoA 还原酶抑制剂，具有有效降低血脂的能力。Atorvastatin hemicalcium trihydrate 以 IC50值分别为 0.39 μM 和 2.39 μM 来抑制人 SV-SMC 细胞的增殖和侵袭。
T73820	Bosentan-d4
	Bosentan-d4 是 Bosentan 的氘代物。Bosentan 是一种有效的endothelin-1 (ET)拮抗剂，在人的 SMC 细胞中，作用于ETA 和ETB 受体，Ki 值分别为 4.7 nM 和 95 nM。
T15127	Difluoro atorvastatin Fluoroatorvastatin	Others	Others
	Difluoro atorvastatin is an Atorvastatin impurity. Atorvastatin is an orally active HMG-CoA reductase inhibitor and it has the ability to effectively decrease blood lipids. Atorvastatin inhibits human SV-SMC proliferation and invasion (IC50s: 0.39 μM and
T60412	BPN-15477
	BPN-15477 是一种剪接调节剂化合物 (SMC)，可恢复 ELP1 外显子 20 的正确剪接。它可用作于额颞叶痴呆研究。 BPN-15477 纠正了 ELP1 转录本的剪接，显着提高了体内所有组织（包括大脑）中功能蛋白的水平。
T20765	Atorvastatin 阿托伐他汀,阿伐他汀	HMG-CoA Reductase; Autophagy	Autophagy; Metabolism
	Atorvastatin 是一种具有口服活性的 HMG-CoA 还原酶抑制剂，通过激活肝细胞色素p450加快代谢，具有有效降低血脂的能力。Atorvastatin 以 IC50 值分别为 0.39 μM 和 2.39 μM 来抑制人 SV-SMC 细胞的增殖和侵袭。Atorvastatin 与氯吡格雷同时服用两种可能会导致患者血栓事件增加。
T67442	CGP-53716
	The growth factors, platelet-derived growth factor (PDGF) and basic fibroblast growth factor (bFGF) play major roles in enhanced smooth muscle cells growth in rodent blood vessels after vascular injury. Tyrosine kinase inhibition has been shown to be effective in blocking tyrosine phosphorylation at the PDGF and bFGF receptors in cultured fibroblast and vascular smooth muscle cells which in turn inhibits their proliferation[1]. CGP 53716 is a specific PDGFR tyrosine kinase inhibitor on SMC (smoo...

化合物

Cat.No: T7133

Synonym: SK-0403,阿拉格列汀

Target: Proteasome, DPP-4

Cat.No: T11917

Synonym: Lys-Nε-MCC-DM1

Target: Microtubule Associated

Cat.No: T16899

Synonym: DM1-SMCC

Target: Others

Sulfo-SMCC sodium

Cat.No: T18728

Target: Others

Cat.No: T9116

Synonym: N-Succinimidyl 4-(N-maleimidomethyl)cycl,4-(N-马来酰亚胺基甲基)环己烷-1-羧酸琥珀酰亚胺酯

Target: Others

Paclitaxel-SMCC

Cat.No: T28289

Synonym: SMCC taxol, Taxol-SMCC, Taxol SMCC,Paclitaxel with SMCC linker,SMCC-Taxol,Paclitaxel ADC conjugate.

Smcy HY Peptide (738-746)

Cat.No: TP1639

Synonym: Smcy HY Peptide 738-746

trans-Sulfo-SMCC

Cat.No: T18856

Target: Others

Doxorubicin-SMCC

Cat.No: T15161

Target: Others

Cat.No: T63090

Cat.No: T18361

Target: Others

Palbociclib-SMCC

Cat.No: T33865

Synonym: PD0332991-SMCC,Palbociclib-SMCC linker,PD 0332991-SMCC,PD-0332991-SMCC

Cat.No: T17833

Target: Others

Rha-PEG3-SMCC

Cat.No: T81280

4-N-Dodecyloxyphenol

Cat.No: T72050

Synonym: 4-dodecoxyphenol,p-Dodecyloxyphenol

Bosentan (hydrate)

Cat.No: T6265

Synonym: 波生坦水合物,Bosentan Hydrate,Benzenesulfonamide,Actelion,Ro 47-0203

Target: Endothelin Receptor

Atorvastatin hemicalcium salt

Cat.No: T3116

Synonym: Lipitor,Atorvastatin hemicalcium,Atorvastatin Calcium,CI-981,阿托伐他汀钙,Sortis

Target: Ferroptosis, HMG-CoA Reductase, Autophagy

Aviptadil Acetate

Cat.No: TP1016L

Synonym: 醋酸阿肽地尔,阿肽地尔,Vasoactive Intestinal Peptide acetate salt

Target: RAAS, SARS-CoV

Cat.No: T6264

Synonym: Actelion,波生坦,Ro 47-0203,Benzenesulfonamide

Target: Endothelin Receptor

Atorvastatin hemicalcium trihydrate

Cat.No: T72101

Synonym: 阿托伐他汀半钙三水合物,阿托他伐汀半钙三水合物

Cat.No: T73820

Difluoro atorvastatin

Cat.No: T15127

Synonym: Fluoroatorvastatin

Target: Others

Cat.No: T60412

Cat.No: T20765

Synonym: 阿托伐他汀,阿伐他汀

Target: HMG-CoA Reductase, Autophagy

Cat.No: T67442

Cat. No.	Product Name	Target	Signaling Pathways
T3805	Prim-O-glucosylcimifugin 升麻苷,Cimifugin beta-D-glucopyranoside,Cimifugin 7-glucoside	TNF; COX; JAK; NO Synthase	Angiogenesis; Apoptosis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; Stem Cells
	Prim-O-glucosylcimifugin (Cimifugin 7-glucoside) 具有强效的抗炎作用。通过调节 JAK2/STAT3 信号传导可抑制iNOS 和COX-2表达。

天然产物

Prim-O-glucosylcimifugin

Cat.No: T3805

Synonym: 升麻苷,Cimifugin beta-D-glucopyranoside,Cimifugin 7-glucoside

Target: TNF, COX, JAK, NO Synthase

我们的所有产品和服务仅用于科学研究，不能被用于人体，我们也不向个人提供产品和服务。

Copyright © 2015-2024 TargetMol Chemicals Inc. All rights reserved. 沪ICP备20019793号-4

沪公网安备 31010602006700号

沪公网安备 31010602006700号

TargetMol Loading

联系我们

电话：

400-820-0310

邮箱：

service@tsbiochem.com

QQ：

2881945090（终端用户）

2885109491（经销商）

经销：

终端：

地址：

上海市静安区江场三路238号8楼