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Search Results for " neuroblastoma "

Targets Recommended: Apoptosis Phosphatase

69

抑制剂 & 化合物

13

天然产物

1

化合物库

11

重组蛋白

1

同位素标记化合物

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Cat. No.	Product Name
L8710	铜死亡化合物库		400 compounds
	TargetMol 铜死亡化合物库集合了 400 种与铜死亡相关的化合物，可以用于铜死亡机制及相关疾病研究

化合物库

铜死亡化合物库

Cat.No: L8710

Compounds: 400

Cat. No.	Product Name	Target	Signaling Pathways
T16350	NSC-87877	Apoptosis; Phosphatase	Apoptosis; Metabolism
	NSC-87877 是一种Shp2和Shp1蛋白质酪氨酸磷酸酶抑制剂，IC50值分别为0.318 μM 和0.355 μM。它还抑制双特异性磷酸酶26。
T6911	NSC-87877 disodium NSC87877	Apoptosis; Phosphatase	Apoptosis; Metabolism
	NSC-87877 disodium (NSC87877) 是一种有效的Shp2和Shp1蛋白质酪氨酸磷酸酶抑制剂，IC50值分别为0.318 μM 和0.355 μM。NSC-87877还抑制双特异性磷酸酶26。
T1841	UNC0379	Histone Methyltransferase	Chromatin/Epigenetic
	UNC0379 是一种选择性的、底物竞争性的赖氨酸甲基转移酶 SETD8 抑制剂，IC50值为 7.3 μM，也选择性抑制其他 15 种甲基转移酶。
T0412	Idebenone 艾地苯醌,CV-2619	Apoptosis; Antioxidant; Mitochondrial Metabolism	Apoptosis; Metabolism; oxidation-reduction
	Idebenone (CV-2619) 是一种线粒体保护剂，具有神经保护功效，可用于研究阿尔茨海默病、亨廷顿舞蹈病，可透过血脑屏障，诱导细胞凋亡。
T8596	Ceefourin 1	MRP	Immunology/Inflammation
	Ceefourin 1 是一种具有高度选择性的多药抗性蛋白 4 (MRP4) 抑制剂。它能够抑制多种 MRP4 底物的转运，但对其他 ABC 转运蛋白无影响。它是苯并噻唑，常作为高危神经母细胞瘤的化学增敏剂。
T9240	sulfopin Acetamide, 2-chloro-N-(2,2-dimethylpropyl)-N-(tetrahydro-1,1-dioxido-3-thienyl)-	Others	Others
	Sulfopin 是高选择性共价Pin1抑制剂(Ki:17 nM)，在体内能够阻断 Myc 驱动的肿瘤。其中肽基脯氨酰异构酶 Pin1 在癌症中被用来激活癌基因和灭活肿瘤抑制因子。
T6609	NMS-E973	HSP	Cytoskeletal Signaling; Metabolism
	NMS-E973 是一种有效且选择性的 Hsp90 抑制剂，与 Hsp90 结合的 DC50小于 10 nM。它能够穿越血脑屏障，具有抗肿瘤效果。
T11908	LY2365109 hydrochloride LY2365109盐酸盐	GlyT	Neuroscience
	LY2365109 hydrochloride 是高选择性GlyT1抑制剂，抑制过表达 hGlyT1 细胞摄取谷氨酸的IC50值为 15.8 nM.
T12165	nAChR agonist 1 DUN71755	AChR	Neuroscience
	nAChR agonist 1 (DUN71755) 是一种脑渗透性和口服有效的正变构 α7 烟碱乙酰胆碱受体 (α7 nAChR) 调节剂。它在 Ca2+中，对内源性表达 α7 nAChR 的人 IMR-32 神经母细胞瘤细胞的EC50为 0.32 μM。它可用于阿尔茨海默病的研究。
T6708	Tolcapone Tasmar,Ro 40-7592,托卡朋	Apoptosis; Beta Amyloid; Transferase	Apoptosis; Metabolism; Neuroscience
	Tolcapone (Ro 40-7592) 是一种选择性，具有口服活性的外周和中枢COMT 抑制剂，在肝脏中对 COMT 的IC50为 773 nM。它还是一种 α-syn 和 Aβ42 寡聚和原纤维形成的有效抑制剂，可诱导氧化应激导致神经母细胞瘤细胞凋亡和抑制肿瘤生长。
T12134	MYCMI-6 NSC354961	Apoptosis; c-Myc	Apoptosis; Cell Cycle/Checkpoint
	MYCMI-6 (NSC-354961) 是一种内源性MYC:MAX 蛋白相互作用抑制剂，选择性结合 MYC bHLHZip 域，Kd 值为 1.6 μM。它阻断 MYC 驱动的转录，以 MYC 依赖性的方式抑制肿瘤细胞的生长，诱导细胞凋亡。
T1967	AZD-3463 ALK/IGF1R inhibitor	Apoptosis; IGF-1R; ALK; Autophagy	Angiogenesis; Apoptosis; Autophagy; Tyrosine Kinase/Adaptors
	AZD-3463 (ALK/IGF1R inhibitor) 是一种具有口服活性的ALK/IGF1R 抑制剂，对 ALK 作用的Ki 值为 0.75 nM。它可诱导神经母细胞瘤细胞凋亡和自噬。
T6611	NSC697923 2-[(4-methylphenyl)sulfonyl]-5-nitrofuran	E1/E2/E3 Enzyme	Ubiquitination
	NSC-697923 (2-[(4-methylphenyl)sulfonyl]-5-nitrofuran), a potent inhibitor of UBE2N (ubiquitin-conjugating enzyme E2 N, Ubc13), exhibits its role in inducing cell death in neuroblastoma (NB) cells through two distinct mechanisms. In p53 wild-type NB cells, NSC-697923 promotes the nuclear importation of p53, thereby triggering cell death. Meanwhile, in p53 mutant NB cells, NSC-697923 activates the JNK-mediated apoptotic pathway, leading to cell death. Additionally, NSC-697923 inhibits DNA damage ...
T3061	Lorlatinib 劳拉替尼,PF-6463922,PF-06463922,Loratinib	Apoptosis; Tyrosine Kinases; ROS; ALK; ROS Kinase	Angiogenesis; Apoptosis; Immunology/Inflammation; Tyrosine Kinase/Adaptors
	Lorlatinib (PF-6463922) 是一种具有口服活性，选择性，脑渗透性和 ATP 竞争性的ROS1/ALK 抑制剂，具有抗癌活性。它对 ROS1、野生型 ALK 和 ALKL1196M 的Ki 值分别为 <0.025 nM、<0.07 nM 和 0.7 nM。
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。
T39733	Hu7691 free base	Akt	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	Hu7691 free base 是一种具有口服活性、高效性和选择性的 Akt 抑制剂，对多种神经母细胞瘤细胞系的抗增殖和神经发生作用。Hu7691 free base 抑制 Akt1、Akt2 和 Akt3 ，诱导神经母细胞瘤细胞分化。
T77495	WDR5-IN-6	JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	WDR5-IN-6 是一种 WDR5 抑制剂，靶向 WBM 位点。WDR5-IN-6 与靶向 WIN 位点的 WDR5 抑制剂 OICR-9429 具有高度协同作用。WDR5-IN-6 具有较强的抗肿瘤活性，可抑制神经母细胞瘤细胞系的细胞增殖。WDR5-IN-6 可用于神经母细胞瘤的研究。
T9068	Cucurbit[7]uril	Others	Others
	Cucurbit[7]uril 是一种新兴的药用辅料候选物。Cucurbit[7]uril 可增强神经母细胞瘤细胞中卟啉的光敏作用。
T4436	RO1138452 CAY10441	Others; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation; Others
	RO1138452 (CAY10441) 是一种选择性和可口服的前列环素受体拮抗剂，pKi 为8.3。它拮抗卡前列环素诱导的人神经母细胞瘤腺苷酸环化酶的激活，以剂量依赖性方式阻断环 AMP 积累，具有镇痛活性。
T77448	Naxitamab Naxitamab-gqgk,Humanized 3F8,Hu3F8	Others	Others
	Naxitamab (Hu3F8) 是一种针对二氮冈糖苷 GD2 (hu3F8)的人源化单克隆抗体。Naxitamab 具有抗肿瘤活性，可用于研究神经母细胞瘤、骨肉瘤和其他 GD2 阳性癌症。
T40363	Poly-D-lysine hydrobromide (MW 30000-70000) Poly-D-lysine HBr (MW 30000-70000)	CaSR	GPCR/G Protein
	Poly-D-lysine hydrobromide (MW 30000-70000)(Poly-D-lysine HBr) 是一种可口服的肽类 CaSR 激动剂，可从朊病毒感染的 SN56 神经母细胞瘤细胞中去除蛋白酶 K 抗性的 PrP。
T3203	Methyl 13-cis-4-Oxoretinoate 13-cis-4-Oxo-retinoic acid Methyl Ester,4-Keto 13-cis-Retinoic Acid Methyl Ester	Others	Others
	Methyl 13-cis-4-Oxoretinoate (13-cis-4-Oxo-retinoic acid Methyl Ester) 是神经母细胞瘤中的一种视黄酸代谢物。
T3690	A-740003 A 740003	P2X Receptor	Membrane transporter/Ion channel; Neuroscience
	A-740003 (A 740003) 是一种选择性和竞争性的P2X7 受体拮抗剂，抑制大鼠和人的 P2X7 受体，IC50值分别为 18 和 40 nM。
T77332	TV 3279	BCL; PKC	Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling
	TV 3279是一种新型ChE-MAI 抑制剂，神经保护特性取决于它们诱导抗凋亡蛋白PKC、Bcl-2、Bcl-x 和SOD 的能力，并阻止促凋亡酶甘油醛磷酸脱氢酶在PC-12和神经母细胞瘤细胞中的核易位。
T16703	Quarfloxin CX-3543	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Quarfloxin (CX-3543) 是一种氟喹诺酮衍生物，具有抗肿瘤活性，可靶向抑制RNA pol I 的活性，在神经母细胞瘤细胞中的 IC50 值在纳摩尔范围内。它破坏核糖体 DNA 模板中核仁蛋白和 G-四链体 DNA 结构之间的相互作用。
T10313	(Rac)-AMXT-1501 4HCl	Dopamine Receptor; Antibacterial	GPCR/G Protein; Microbiology/Virology; Neuroscience
	(Rac)-AMXT-1501 4HCl 是一种多胺转运抑制剂,抑制多胺转运与顺铂在 HNSCC 中协同作用。(Rac)-AMXT-1501 4HCl 具有潜在的抗菌活性，通过靶向鸟氨酸脱羧酶和多胺转运抑制神经母细胞瘤细胞增殖，抑制肺炎球菌的荚膜生物合成。
T16550	PKR-IN-C16	Others	Others
	PKR-IN-C16 是一种特异性蛋白激酶抑制剂。它能够抑制 PKR 的自磷酸化，解除 PKR 在原代神经元细胞培养中诱导的翻译阻断。
T77651	Tubulin polymerization-IN-47	Microtubule Associated	Cytoskeletal Signaling
	Tubulin polymerization-IN-47 是一种 tubulin 聚合抑制剂和有丝分裂抑制剂，具有抗肿瘤活性，对神经母细胞瘤癌细胞增殖具有抑制作用，对 Chp-134 和 Kelly 细胞系的IC50 分别为 7 和 12 nM。Tubulin polymerization-IN-47 是治疗肝癌、结肠癌、肺癌和乳腺癌的候选化合物。
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。
T1758	ABT-751 E7010	Microtubule Associated; Autophagy	Autophagy; Cytoskeletal Signaling
	ABT-751 (E7010) 是一种新型的生物相容性的微管蛋白结合剂，用于治疗肺癌、非小细胞肺癌和非小细胞肺癌。它是磺胺类抗有丝分裂抑制剂，对神经母细胞瘤细胞株和非神经母细胞瘤细胞株的IC50分别为1.5 和 3.4 μM。
T41180	JQAD1	Epigenetic Reader Domain; PROTACs	Chromatin/Epigenetic; PROTAC
	JQAD1是一种有效的、选择性的组蛋白乙酰转移酶 EP300降解剂（PROTAC；DC50≤31.6nM）；其包含 EP300抑制剂A485，通过连接体连接至脑啡肽E3连接酶配体。JQAD1以蛋白酶体依赖的方式导致神经母细胞瘤细胞系中EP300的降解。JQAD1抑制H3K27ac 和EP300的表达水平并诱导细胞凋亡。JQAD1抑制Kelly 细胞异种移植的NSG 小鼠的肿瘤生长。CRC 和MYCN 基因表达水平在JQAD1治疗的肿瘤中下调。JQAD1在诱导EP300降解的浓度下对共活化剂CBP 没有显著影响。
T61268	Vutiglabridin HSG4112	Phosphatase	Metabolism
	Vutiglabridin (HSG4112) 是一种新型且安全的PON2调节剂，是一个外消旋化合物。Vutiglabridin 是Glabridin 的优化结构类似物，比Glabridin 在减重效果和化学稳定性方面更加优越。Vutiglabridin 通过靶向线粒体对氧磷酶-2改善mptp 诱导的帕金森病小鼠的神经变性。Vutiglabridin 是一种治疗肥胖的临床2期药物，在PD 模型中对对线粒体PON2具有治疗作用。Vutiglabridin 渗透到大脑，结合PON2，恢复1-甲基-4-苯基吡啶(MPP*)诱导的SH-SY5Y 神经母细胞瘤细胞线粒体功能障碍。Vutiglabridin 在小鼠实验中显著减轻了1-甲基-4苯基-1,2,3,6-四氢吡啶(MPTP)诱导的PD 模型小鼠的运动障碍和多巴胺能神经元损伤。
T5343	UAMC-3203 UAMC 3203,UAMC3203	Ferroptosis	Apoptosis
	UAMC-3203 是一种有效的选择性铁死亡抑制剂，IC50为12 nM。
T26412	A 274 A-274,A274	Others	Others
	A 274 is a highly aromatic, monosubstituted phenol antioxidant generated during differentiation of neuroblastoma cells.
T39899	Hu7691	Akt	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	Hu7691 是一种具有口服活性、选择性和高效性的 Akt 抑制剂，抑制 Akt1、Akt2 和 Akt3，抑制神经母细胞瘤细胞增殖，诱导神经母细胞瘤细胞的分化。
T29030	U-101958 Maleate U101958,U-101958,U 101958	Others	Others
	U-101958 Maleate is a ligand of dopamine D4 receptor. U-101958 Maleate also binds to a large sigma1 receptor-like component in SK-N-MC neuroblastoma cells and human cerebellum with high affinity.
T69346	A-357300	Others	Others
	A-357300 is a potent, selective, reversible MetAP2 inhibitor with IC50 of 0.12 uM. Methionine aminopeptidase 2 inhibition is an effective treatment strategy for neuroblastoma in preclinical models.
T27655	JG-48	Others	Others
	JG-48 is an inhibitor of Hsp70. JG-48 suppresses phosphorylated and total Tau in cells, endogenous Tau in neuroblastoma cells.
T70427	CB-64D	Others	Others
	CB-64D is a sigma2R selective agonist which releases calcium in human neuroblastoma cells and produces cell death in tumor cell lines.
T15412	GPP78 CAY10618	Autophagy	Autophagy
	GPP78 is a potent inhibitor of Nampt (IC50: 3.0 nM for nicotinamide adenine dinucleotide (NAD) depletion). GPP78 is cytotoxic to neuroblastoma cell line SH-SY5Y cells (IC50: 3.8 nM by inducing autophagy). GPP78 has anti-cancer and anti-inflammatory effect
T70284	Epolactaene	Others	Others
	Epolactaene is a neuritogenic compound in human neuroblastoma cells which selectively inhibit the activities of mammalian DNA polymerases and human DNA topoisomerase II.
T10589	BPN-15606 besylate (1914989-49-3 free base) BPN-15606 besylate	Others	Others
	BPN-15606 besylate is a highly potent, orally active γ-secretase modulator, attenuates the production of Aβ40 and Aβ42 by SHSY5Y neuroblastoma cells (IC50s: 7 nM and 17nM).
T71026	MC2050 HCl	Others	Others
	MC2050 is a potent PARP-1 inhibitor. The IC50 for inhibition of PARP-1 activity is 119 nM, compared to 1.8 μM for PARP-2. MC2050 inhibits apoptosis and blocks poly ADP-ribosylation of histone H1 in hydrogen peroxide treated SH-SY5Y neuroblastoma cells.
T70224	Bupivacaine tartrate	Others	Others
	Bupivacaine is a BK/SK, Kv1, Kv3, TASK-2 K Channel and voltage-gated Na channel blocker used as an anesthetic. It maybe neurotoxic at high does, inducing apoptosis in neuroblastoma cells. It acts by binding to the intracellular portion of voltage-gated sodium channels and blocking sodium influx into nerve cells.
T38753	CR-1-31-B	Others	Others
	CR-1-31-B, a synthetic rocaglate, acts as a highly potent inhibitor of eIF4A. By disrupting the interaction between eIF4A and RNA, it effectively obstructs the initiation phase of protein synthesis. Specifically, CR-1-31-B interferes with the association between Plasmodium falciparum eIF4A (PfeIF4A) and RNA. Additionally, CR-1-31-B induces apoptosis in neuroblastoma and gallbladder cancer cells [4].
T70151	MeTC7	Others	Others
	MeTC7 is a VDR antagonist, which can be synthesized from 7-dehydrocholesterol (6) in two steps, inhibits VDR selectively, suppresses the viability of cancer cell-lines, and reduces the growth of the spontaneous transgenic TH-MYCN neuroblastoma and xenografts in vivo.
T69149	L2-b	Others	Others
	L2-b is a bifunctional Aβ-interacting, metal-chelating molecule that modulates ROS production in, and improves survival of neuroblastoma cells incubated in the presence of Aβ along with Copper or Zinc. In cell-free aggregation studies, L2-b inhibits metal-induced Aβ aggregation, and also promotes the dissociation of Ab aggregates in homogenates of human AD brain samples.
T10589L	BPN-15606	Others	Others
	BPN-15606 is a highly potent, orally active γ-secretase modulator (GSM), attenuates the production of Aβ42 and Aβ40 by SHSY5Y neuroblastoma cells with IC50 values of 7 nM and 17nM, respectively. BPN-15606 has acceptable PK/PD properties, including bioavai
T68403	AZD-6918	Others	Others
	AZD6918 is a novel potent and selective inhibitor of the Trk tyrosine kinases. AZD-6918 attenuates the BDNF/TrkB-induced protection of neuroblastoma cells from etoposide in vitro and in vivo. AZD6918 inhibited wild-type TrkB-induced cell migration and cell growth.
T77101	Nivatrotamab
	Nivatrotamab (Hu3F8-BsAb)是一种针对GD2和CD3的人源化双特异性抗体，作为基于CD3和GD2特异性bsAb的T细胞接合剂，主要用于神经母细胞瘤的研究。

化合物

Cat.No: T16350

Target: Apoptosis, Phosphatase

NSC-87877 disodium

Cat.No: T6911

Synonym: NSC87877

Target: Apoptosis, Phosphatase

Cat.No: T1841

Target: Histone Methyltransferase

Cat.No: T0412

Synonym: 艾地苯醌,CV-2619

Target: Apoptosis, Antioxidant, Mitochondrial Metabolism

Cat.No: T8596

Target: MRP

Cat.No: T9240

Synonym: Acetamide, 2-chloro-N-(2,2-dimethylpropyl)-N-(tetrahydro-1,1-dioxido-3-thienyl)-

Target: Others

Cat.No: T6609

Target: HSP

LY2365109 hydrochloride

Cat.No: T11908

Synonym: LY2365109盐酸盐

Target: GlyT

nAChR agonist 1

Cat.No: T12165

Synonym: DUN71755

Target: AChR

Cat.No: T6708

Synonym: Tasmar,Ro 40-7592,托卡朋

Target: Apoptosis, Beta Amyloid, Transferase

Cat.No: T12134

Synonym: NSC354961

Target: Apoptosis, c-Myc

Cat.No: T1967

Synonym: ALK/IGF1R inhibitor

Target: Apoptosis, IGF-1R, ALK, Autophagy

Cat.No: T6611

Synonym: 2-[(4-methylphenyl)sulfonyl]-5-nitrofuran

Target: E1/E2/E3 Enzyme

Cat.No: T3061

Synonym: 劳拉替尼,PF-6463922,PF-06463922,Loratinib

Target: Apoptosis, Tyrosine Kinases, ROS, ALK, ROS Kinase

Cat.No: T29541

Synonym: AC-265347

Target: CaSR

Hu7691 free base

Cat.No: T39733

Target: Akt

Cat.No: T77495

Target: JAK

Cucurbit[7]uril

Cat.No: T9068

Target: Others

Cat.No: T4436

Synonym: CAY10441

Target: Others, Prostaglandin Receptor

Cat.No: T77448

Synonym: Naxitamab-gqgk,Humanized 3F8,Hu3F8

Target: Others

Poly-D-lysine hydrobromide (MW 30000-70000)

Cat.No: T40363

Synonym: Poly-D-lysine HBr (MW 30000-70000)

Target: CaSR

Methyl 13-cis-4-Oxoretinoate

Cat.No: T3203

Synonym: 13-cis-4-Oxo-retinoic acid Methyl Ester,4-Keto 13-cis-Retinoic Acid Methyl Ester

Target: Others

Cat.No: T3690

Synonym: A 740003

Target: P2X Receptor

Cat.No: T77332

Target: BCL, PKC

Cat.No: T16703

Synonym: CX-3543

Target: DNA/RNA Synthesis

(Rac)-AMXT-1501 4HCl

Cat.No: T10313

Target: Dopamine Receptor, Antibacterial

Cat.No: T16550

Target: Others

Tubulin polymerization-IN-47

Cat.No: T77651

Target: Microtubule Associated

Cat.No: T26174

Synonym: SAK 3,SAK-3

Target: Calcium Channel, AChR

Cat.No: T1758

Synonym: E7010

Target: Microtubule Associated, Autophagy

Cat.No: T41180

Target: Epigenetic Reader Domain, PROTACs

Cat.No: T61268

Synonym: HSG4112

Target: Phosphatase

Cat.No: T5343

Synonym: UAMC 3203,UAMC3203

Target: Ferroptosis

Cat.No: T26412

Synonym: A-274,A274

Target: Others

Cat.No: T39899

Target: Akt

U-101958 Maleate

Cat.No: T29030

Synonym: U101958,U-101958,U 101958

Target: Others

Cat.No: T69346

Target: Others

Cat.No: T27655

Target: Others

Cat.No: T70427

Target: Others

Cat.No: T15412

Synonym: CAY10618

Target: Autophagy

Cat.No: T70284

Target: Others

BPN-15606 besylate (1914989-49-3 free base)

Cat.No: T10589

Synonym: BPN-15606 besylate

Target: Others

Cat.No: T71026

Target: Others

Bupivacaine tartrate

Cat.No: T70224

Target: Others

Cat.No: T38753

Target: Others

Cat.No: T70151

Target: Others

Cat.No: T69149

Target: Others

Cat.No: T10589L

Target: Others

Cat.No: T68403

Target: Others

Cat.No: T77101

Cat. No.	Product Name	Target	Signaling Pathways
T1166	Ellipticine 玫瑰树碱,NSC 71795,Elliptisine	Topoisomerase	DNA Damage/DNA Repair
	Ellipticine (Elliptisine) 是一种有效的抗肿瘤剂，抑制 DNA 拓扑异构酶 II 活性，对白血病、神经母细胞瘤和胶质母细胞瘤有部分活性。
T3787	Didymin Isosakuranetin-7-O-rutinoside,Neoponcirin,香风草甙	Apoptosis; Others	Apoptosis; Others
	Didymin (Neoponcirin) 从柑橘类水果中提取的一种膳食类黄酮苷，具有抗氧化特性。它通过抑制 N-Myc 和上调 RKIP 诱导凋亡。
TN1933	Mitraphylline 帽柱木菲碱,帽柱叶碱	IL Receptor; TNF; NF-κB	Apoptosis; Immunology/Inflammation; NF-κB
	Mitraphylline 是一种绒毛钩藤中主要的五环吲哚类生物碱，可阻碍脂多糖介导的原代人中性粒细胞活化。
T5229	DL -3,4-Dihydroxymandelic acid	Others	Others
	DL -3,4-Dihydroxymandelic acid 是去甲肾上腺素在人体中的次要代谢物。神经母细胞瘤患者的 3,4-二羟基扁桃酸水平升高。
T3S1589	Notoginsenoside Fa	Others	Others
	Notoginsenoside Fa 是一种原人参二醇型皂苷，从P. notoginseng 提取出来得到，有激活和恢复退化脑功能的潜能。
T13354	Xanthoangelol	Apoptosis; Monoamine Transporter; Antibacterial; AMPK	Apoptosis; Chromatin/Epigenetic; Membrane transporter/Ion channel; Microbiology/Virology; PI3K/Akt/mTOR signaling
	Xanthoangelol 可从 Angelica keiskei 中提取得到，对肥胖引起的炎症反应有抑制作用。Xanthoangelol 具有抗菌活性，对单胺氧化酶有抑制作用，还诱导神经母细胞瘤和白血病细胞凋亡。
T3803	Specnuezhenide 特女贞苷,Nuzhenide,Nuezhenide	Others; NF-κB; Wnt/beta-catenin	Cytoskeletal Signaling; NF-κB; Others; Stem Cells
	Specnuezhenide (Nuezhenide) 是分离自女贞子的果实中。它可抑制 NF-κB 和 wnt/β-catenin 信号传导，进而抑制 IL-1β 诱导的软骨细胞炎症。它可在骨关节炎 (OA) 大鼠模型中发挥抗炎作用。
T6718	Zingerone Gingerone,Vanillylacetone,姜酮,NSC 15335	NF-κB	NF-κB
	Zingerone (Vanillylacetone) 是一种从生姜中得到的无毒的甲氧基苯酚，具有抗炎、抗糖尿病、抗脂质过敏、抗腹泻、抗痉挛和抗肿瘤等活性。它作为抗有丝分裂剂，能够抑制神经母细胞瘤的生长。它能够缓解氧化应激和炎症，下调 NF-κB 介导的信号通路。
T73640	Pancratistatin	Others	Others
	Pancratistatin 是一种异喹啉生物碱，可以从蜘蛛兰 Hymenocallis littoralis 中分离。Pancratistatin 诱导人黑素瘤细胞凋亡。Pancratistatin 可用于神经母细胞瘤、白血病、和乳腺癌的研究。
TN6062	1,3,9-Trimethyluric acid
	1,3,9-Trimethyluric acid exhibits in vitro cytotoxic activity against breast cancer (MCF-7), human neuroblastoma (SHSY5Y), human non-small cell lung cancer (A549) and human liver cancer (HEPG2) with IC50 value in the range of 1-3 uM. 1,3,9-Trimethyluric a
T36954	Nemorosone	Others	Others
	Nemorosone is a polycyclic polyprenylated acylphloroglucinol (PPAP) originally isolated from C. rosea that has antiproliferative properties.1 Nemorosone inhibits growth of NB69, Kelly, SK-N-AS, and LAN-1 neuroblastoma cells (IC50s = 3.1-6.3 μM), including several drug-resistant clones, but not MRC-5 human embryonic fibroblasts (IC50 = >40 μM).2 It increases DNA fragmentation in LAN-1 cells in a dose-dependent manner, and decreases N-Myc protein levels and phosphorylation of ERK1/2 by MEK1/2. Nem...
TN6685	Homovanillic Acid Sulfate
	Homovanillic acid sulfate is used as a reagent to detect oxidative enzymes, and is associated with dopamine levels in the brain.In psychiatry and neuroscience, brain and cerebrospinal fluid levels of homovanillic acid are measured as a marker of metabolic
TN3614	Cearoin 檀木	ERK; BCL; PARP; IκB/IKK; TNF; NF-κB; ROS; Caspase	Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; MAPK; NF-κB; Proteases/Proteasome
	Cearoin has anti-inflammatory, and antiallergic activities, it can markedly inhibit inflammatory responses including LPS-induced NO production by suppressing the expression of iNOS mRNA and LPS-induced mRNA expression of TNFα and CCL2. Cearoin induces aut

天然产物

Cat.No: T1166

Synonym: 玫瑰树碱,NSC 71795,Elliptisine

Target: Topoisomerase

Cat.No: T3787

Synonym: Isosakuranetin-7-O-rutinoside,Neoponcirin,香风草甙

Target: Apoptosis, Others

Cat.No: TN1933

Synonym: 帽柱木菲碱,帽柱叶碱

Target: IL Receptor, TNF, NF-κB

DL -3,4-Dihydroxymandelic acid

Cat.No: T5229

Target: Others

Notoginsenoside Fa

Cat.No: T3S1589

Target: Others

Cat.No: T13354

Target: Apoptosis, Monoamine Transporter, Antibacterial, AMPK

Cat.No: T3803

Synonym: 特女贞苷,Nuzhenide,Nuezhenide

Target: Others, NF-κB, Wnt/beta-catenin

Cat.No: T6718

Synonym: Gingerone,Vanillylacetone,姜酮,NSC 15335

Target: NF-κB

Cat.No: T73640

Target: Others

1,3,9-Trimethyluric acid

Cat.No: TN6062

Cat.No: T36954

Target: Others

Homovanillic Acid Sulfate

Cat.No: TN6685

Cat.No: TN3614

Synonym: 檀木

Target: ERK, BCL, PARP, IκB/IKK, TNF, NF-κB, ROS, Caspase

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPY-02670	NBL1 Protein, Mouse, Recombinant (His) neuroblastoma 1, DAN family BMP antagonist,DAN,NO3,...	Mouse	HEK293 Cells
	NBL1 Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 18.8 kDa and the accession number is Q61477.
TMPY-00771	NBL1 Protein, Human, Recombinant (hFc) neuroblastoma 1, DAN family BMP antagonist,NO3,NB,D...	Human	HEK293 Cells
	NBL1 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 44.4 kDa and the accession number is P41271-1.
TMPY-01039	NBL1 Protein, Human, Recombinant (His) neuroblastoma 1, DAN family BMP antagonist,NO3,DAN,...	Human	HEK293 Cells
	NBL1 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 19.3 kDa and the accession number is P41271-1.
TMPY-03487	NRAS Protein, Human, Recombinant (His) NS6,NCMS,CMNS,neuroblastoma RAS viral (v-ras) oncog...	Human	E. coli
	NRAS was discovered by researchers at the Institute of Cancer Research, funded by the Cancer Research Campaign (now Cancer Research UK). NRAS gene is a member of the Ras gene family. It is mapped on chromosome 1, and it is activated in HL6, a promyelocytic leukemia line. The mammalian ras gene family consists of the Harvey and Kirsten ras genes (HRAS and KRAS), an inactive pseudogene of each (c-Hras2 and c-Kras1), and the N-ras gene. They differ significantly only in the C-terminal 4 amino acids...
TMPH-01775	N-myc Protein, Human, Recombinant (His) MYCN,Class E basic helix-loop-helix protein 37,N-myc proto-o...	Human	P. pastoris (Yeast)
	Positively regulates the transcription of MYCNOS in neuroblastoma cells. N-myc Protein, Human, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 51.6 kDa and the accession number is P04198.
TMPY-03410	TMEM25 Protein, Human, Recombinant (His) bA83N9.1,transmembrane protein 25	Human	HEK293 Cells
	TMEM25 is a novel member of the immunoglobulin superfamily. Immunoglobulin superfamily members are implicated in immune responses, growth factor signaling, and cell adhesion. TMEM25 contains 1 Ig-like (immunoglobulin-like) domain and is a target of pharmacogenomics in the field of oncology and regenerative medicine. TMEM25 isoform 1, consisting of exons 1-9, encoded a 366-aa transmembrane protein. TMEM25 isoform 2, consisting of exons 1-4 and 6-9, encoded a 322-aa secreted protein. TMEM25 mRNA w...
TMPY-02945	Prokineticin 1/EG-VEGF Protein, Human, Recombinant (His) PK1,EGVEGF,PRK1,prokineticin 1	Human	Baculovirus Insect Cells
	EG-VEGF, also known as prokineticin-1, is a member of the AVIT (prokineticin) family. Prokineticins are secreted proteins that can promote angiogenesis and induce strong gastrointestinal smooth muscle contraction. EG-VEGF can be detected in the steroidogenic glands, ovary, testis, adrenal and placenta. EG-VEGF has little or no effect on a variety of other endothelial and non-endothelial cell types. It induces proliferation, migration and fenestration (the formation of membrane discontinuities) i...
TMPH-02842	CD133/PROM1 Protein, Mouse, Recombinant (His & SUMO) CD133,Prom1,Prominin-like protein 1,Prom,Proml1,Antigen AC13...	Mouse	E. coli
	May play a role in cell differentiation, proliferation and apoptosis. Binds cholesterol in cholesterol-containing plasma membrane microdomains and may play a role in the organization of the apical plasma membrane in epithelial cells. During early retinal development acts as a key regulator of disk morphogenesis. Involved in regulation of MAPK and Akt signaling pathways. In neuroblastoma cells suppresses cell differentiation such as neurite outgrowth in a RET-dependent manner.
TMPH-01609	LGI1 Protein, Human, Recombinant (His & Myc) Leucine-rich glioma-inactivated protein 1,Epitempin-1,LGI1	Human	E. coli
	Regulates voltage-gated potassium channels assembled from KCNA1, KCNA4 and KCNAB1. It slows down channel inactivation by precluding channel closure mediated by the KCNAB1 subunit. Ligand for ADAM22 that positively regulates synaptic transmission mediated by AMPA-type glutamate receptors. Plays a role in suppressing the production of MMP1/3 through the phosphatidylinositol 3-kinase/ERK pathway. May play a role in the control of neuroblastoma cell survival.
TMPH-00001	CD133/PROM1 Protein-VLP, Human, Recombinant (His) Proml1,Prom1,CD133,Prominin-like protein 1,Antigen AC133 hom...	Human	HEK293 Cells
	May play a role in cell differentiation, proliferation and apoptosis. Binds cholesterol in cholesterol-containing plasma membrane microdomains and may play a role in the organization of the apical plasma membrane in epithelial cells. During early retinal development acts as a key regulator of disk morphogenesis. Involved in regulation of MAPK and Akt signaling pathways. In neuroblastoma cells suppresses cell differentiation such as neurite outgrowth in a RET-dependent manner. CD133/PROM1 Protein...
TMPY-01308	AGO1 Protein, Human, Recombinant (His) EIF2C,GERP95,argonaute RISC catalytic component 1,EIF2C1,Q99	Human	Baculovirus Insect Cells
	Protein argonaute-1, also known as eukaryotic translation initiation factor 2C 1, EIF2C1, and AGO1, is a member of the argonaute family and ago subfamily. Protein argonaute-1 in humans is encoded by the EIF2C1 gene. This gene is located on chromosome 1 in a cluster of closely related family members including argonaute 3, and argonaute 4. This genomic region is frequently lost in human cancers such as Wilms tumors, neuroblastoma, and carcinomas of the breast, liver, and colon. The human EIF...

重组蛋白

NBL1 Protein, Mouse, Recombinant (His)

Cat.No: TMPY-02670

Species: Mouse

Expression System: HEK293 Cells

NBL1 Protein, Human, Recombinant (hFc)

Cat.No: TMPY-00771

Species: Human

Expression System: HEK293 Cells

NBL1 Protein, Human, Recombinant (His)

Cat.No: TMPY-01039

Species: Human

Expression System: HEK293 Cells

NRAS Protein, Human, Recombinant (His)

Cat.No: TMPY-03487

Species: Human

Expression System: E. coli

N-myc Protein, Human, Recombinant (His)

Cat.No: TMPH-01775

Species: Human

Expression System: P. pastoris (Yeast)

TMEM25 Protein, Human, Recombinant (His)

Cat.No: TMPY-03410

Species: Human

Expression System: HEK293 Cells

Prokineticin 1/EG-VEGF Protein, Human, Recombinant (His)

Cat.No: TMPY-02945

Species: Human

Expression System: Baculovirus Insect Cells

CD133/PROM1 Protein, Mouse, Recombinant (His & SUMO)

Cat.No: TMPH-02842

Species: Mouse

Expression System: E. coli

LGI1 Protein, Human, Recombinant (His & Myc)

Cat.No: TMPH-01609

Species: Human

Expression System: E. coli

CD133/PROM1 Protein-VLP, Human, Recombinant (His)

Cat.No: TMPH-00001

Species: Human

Expression System: HEK293 Cells

AGO1 Protein, Human, Recombinant (His)

Cat.No: TMPY-01308

Species: Human

Expression System: Baculovirus Insect Cells

Cat. No.	Product Name	Target	Signaling Pathways
T70882	Orlistat-d3
	Orlistat-d3 is intended for use as an internal standard for the quantification of orlistat by GC- or LC-MS. Orlistat is a digestive lipase inhibitor. It inhibits diacylglycerol lipase α (DAGLα), DAGLβ, α/β-hydrolase domain-containing protein 12 (ABHD12), ABHD16A, and platelet-activating factor acetylhydrolase (PAF-AH; IC50s = 0.06, 0.1, 0.08, 0.03, and 0.05 µM, respectively), as well as pancreatic lipase and hormone-sensitive lipase (IC50s = 0.65 and 2.1 µg/ml, respectively) but does not inhibit...

同位素标记化合物

Cat.No: T70882

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