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Search Results for " acute lymphoblastic leukemia "

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Cat. No.	Product Name	Target	Signaling Pathways
T7955	EB-3D	Apoptosis; AMPK; AChR	Apoptosis; Chromatin/Epigenetic; Neuroscience; PI3K/Akt/mTOR signaling
	EB-3D 是一种选择性胆碱激酶 α 抑制剂，对 ChoKα1 的IC50值为 1 μM。它影响 ChoKα 表达、AMPK 激活、细胞凋亡、内质网应激和脂质代谢，具有抗癌活性。
T12943	SNDX-5613	Epigenetic Reader Domain; Histone Methyltransferase	Chromatin/Epigenetic
	SNDX-5613 是一种 Menin-MLL 特异性抑制剂，Ki 为 0.149 nM，IC50 为 10 在 20 nM 之间，可用于 MLL 基因重排的急性白血病研究。
T8308	NL-1	Mitochondrial Metabolism; Autophagy	Autophagy; Metabolism
	NL-1 是一种mitoNEET 抑制剂，具有抗白血病作用。它抑制 REH 和 REH/Ara-C 细胞生长，IC50分别为 47.35 µM 和 56.26 µM。
TP1115	L-Asparaginase L-ASNase	Others	Others
	L-Asparaginase (L-ASNase) 是催化 L-天冬酰胺转化的水解酶，从血浆中去除 L-天冬酰胺，导致 RNA 和 DNA 合成抑制，随后引起细胞凋亡。它用于急性淋巴细胞白血病的研究。
T16545	Pivanex Pivalyloxymethyl butyrate,AN-9	Apoptosis; HDAC; Bcr-Abl	Angiogenesis; Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Tyrosine Kinase/Adaptors
	Pivanex (Pivalyloxymethyl butyrate) 是丁酸的一种衍生物，是具有口服活性的 HDAC 抑制剂。Pivanex 通过下调 bcr-abl 蛋白增强凋亡。Pivanex 显示出抗转移和抗血管生成的活性。
T0370	Pheniramine maleate Daneral,Inhiston,Trimetose,马来酸非尼拉敏	5-HT Receptor; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Pheniramine maleate (Trimetose) 是一种具有抗组胺和血管扩张特性的烷基胺衍生物，可与组胺 H1 受体结合，从而抑制磷脂酶 A2 和内皮源性松弛因子一氧化氮的产生。
T1477	AICAR NSC105823,AICA Riboside,Acadesine,阿卡地新,AICAR (Acadesine)	Mitophagy; YAP; AMPK; Autophagy	Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling; Stem Cells
	AICAR (NSC105823) 是一种腺苷类似物，是一种 AMP 激活的蛋白激酶激活剂，可用于治疗急性淋巴细胞白血病和糖尿病。
T74710	YX-2-107	CDK; PROTACs	Cell Cycle/Checkpoint; PROTAC
	YX-2-107 是一种具有选择性和高效性的降解 CDK6 的 PROTAC ，IC50 值为 4.4 nM。YX-2-107 在体外对 RB 磷酸化和 FOXM1 表达有抑制作用，对大鼠体内 Ph+ ALL 的发展有抑制作用。YX-2-107 可用于预防和治疗 Ph 染色体阳性 (Ph+) 急性淋巴细胞白血病 (ALL)。
T72984	(Rac)-SHIN2	Others	Others
	(Rac)-SHIN2 是一种丝氨酸羟甲基转移酶 (SHMT) 抑制剂，可提高 NOTCH1 驱动的小鼠原代 T-ALL 在体内的存活率，可用于研究 T 细胞急性淋巴细胞白血病（T-ALL）。
T76790	Inotuzumab	Others	Others
	Inotuzumab (Humanized Anti-CD22 Recombinant Antibody) 是人源化靶向 CD22 的 IgG4 抗体。Inotuzumab 是 Inotuzumab ozogamicin 的裸抗，可用于合成抗体-活性分子偶联物 (Inotuzumab ozogamicin)。Inotuzumab 可于研究急性淋巴细胞白血病和非霍奇金淋巴瘤。
T21302L	UNC 569 hydrochloride UNC 569 hydrochloride (1350547-65-7 Free base)	TAM Receptor; TAM Receptor	Tyrosine Kinase/Adaptors
	UNC 569 hydrochloride 是一种可逆的 ATP 竞争性 Mer 抑制剂，IC50 为 2.9 nM，Ki 为 4.3 nM。 UNC 569 hydrochloride 抑制 Axl 和 Tyro3，IC50 分别为 37 nM 和 48 nM。 UNC 569 hydrochloride 可用于关于急性淋巴细胞白血病和非典型畸胎样/横纹肌样肿瘤的研究。
T36944	Ara-G	Nucleoside Antimetabolite/Analog	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Ara-G 是一种脱氧鸟苷 (GdR) 类似物和核苷类似物，可被 T 淋巴谱系细胞迅速转化为其相应的阿拉伯糖基鸟嘌呤核苷酸三磷酸 (araGTP)，从而抑制 DNA 合成和对 T 淋巴母细胞的选择性体外毒性细胞系以及来自 T 细胞急性淋巴细胞白血病 (ALL) 患者的新鲜分离的白血病细胞。
T30688	Calaspargase pegol
	Calaspargase pegol is used to treat acute lymphoblastic leukemia.
T20858	Metanilic acid m-Anilinesulfonic acid,m-Sulfanilic acid
	Metanilic acid, an anti-cancer drug, is used to treat several malignancies including choriocarcinoma and pediatric acute lymphoblastic leukemia.
T24189	J9 J-9,J 9
	J9 is an inhibitor of Glucocorticoid resistance. J9 reverses Dexamethasone Resistance in T-cell Acute Lymphoblastic Leukemia.
T21301	Lesinurad sodium Lesinurad,RDEA 594,RDEA-594,RDEA594
	UNC569, the first small-molecule MER inhibitor, inhibits Mer activation and downstream signaling through ERK1/2 and AKTwith. UNC569 shows efficacy against acute lymphoblastic leukemia in vitro and in vivo.
T36575	HDAC3 Inhibitor
	HDAC3 inhibitor is an allosteric inhibitor of histone deacetylase 3 (HDAC3; Ki = 0.16 nM). It is selective for HDAC3 over HDAC1 and HDAC2 (IC50s = 0.95, 11.81, and 95.45 nM, respectively, using recombinant HDACs). In addition, it is selective for acute myeloid, monocytic, and lymphoblastic leukemia cell lines (EC50s = 36.37, 76.64, and 151.7 nM, respectively) over chronic myeloid, acute promyelocytic, and acute lymphoblastic cells (EC50s = 2,160, >10,000, and >10,000 nM, respectively).
T31672	Erythrofuranosyladenine 9-β-D-Erythrofuranosyladenine,ETA
	Erythrofuranosyladenine(9-beta-D-Erythrofuranosyladenine, ETA) is a nontoxic MTAP substrate. Erythrofuranosyladenine is an effective salvage agent for methylthioadenosine phosphorylase–selective therapy of T-cell acute lymphoblastic leukemia with L-alanos
T79377	NWP-0476
	NWP-0476为针对BCL-2/BCL-xL的抑制剂，其结构已优化以提高对BCL-xL的选择性。该化合物适用于复发性T-急性淋巴细胞白血病（T-ALL）的相关研究。
T78317	Blinatumomab Anatumomab
	Blinatumomab（亦称Anatumomab）是针对B细胞表面CD19抗原的双特异性单克隆抗体，主要用于急性淋巴细胞白血病的研究。
T39799	S2157 S2157
	S2157, a potent N-alkylated tranylcypromine (TCP) derivative lysine-specific demethylase 1 (LSD1) inhibitor, enhances H3K9 methylation and concurrently reduces H3K27 acetylation at super-enhancer sites. This compound triggers apoptosis in TCP-resistant T-cell acute lymphoblastic leukemia (T-ALL) cells by inhibiting NOTCH3 and TAL1 gene expression. Moreover, S2157 is capable of crossing the blood-brain barrier, effectively eliminating central nervous system (CNS) leukemia in mice models implanted...
T4310L2	Prexasertib mesylate LY-2606368,LY2606368,LY 2606368
	Prexasertib is a potent and selective Chk1/Chk2 inhibitor. Prexasertib increases the effectiveness of conventional therapy in B-/T- cell progenitor acute lymphoblastic leukemia. LY2606368 causes replication catastrophe and antitumor effects through CHK1-d
T76801	Denintuzumab
	Denintuzumab (hBU 12) 是一种重组人源化抗 CD19单克隆抗体。Denintuzumab 可作为抗体偶联活性分子的抗体部分 (ADC antibody) 合成 ADC，Denintuzumab Mafodotin (SGN-CD19A)。Denintuzumab Mafodotin 可用于急性淋巴细胞白血病的研究。
T74538	Galectin-3 antagonist 2	Galectin	Immunology/Inflammation
	Galectin-3，作为β-半乳糖苷特异性的识别蛋白（凝集素），具备促进B细胞前体急性淋巴细胞白血病（BCP-ALL）细胞迁移及耐受药物治疗的功能。
T37068	NR-160
	NR-160 is an inhibitor of histone deacetylase 6 (HDAC6; IC50= 0.03 μM).1It is selective for HDAC6 over HDAC1, -2, -3, -4, and -8 (IC50s = 5.18, 2.26, 8.48, 55.4, and 14.7 μM, respectively). NR-160 is cytotoxic against a panel of seven cancer cell lines (IC50s = 22.5-51.8 μM). It enhances cytotoxicity induced by bortezomib in HL-60 cells, as well as cytotoxicity induced by epirubicin or daunorubicin in CCRF-HSB-2 T cell acute lymphoblastic leukemia cells.
T76893	Lusvertikimab
	Lusvertikimab (OSE-127) 是一种人源化IL7R 单克隆抗体。Lusvertikimab 不会被靶细胞内化并阻止 IL7R 异二聚化和随后的下游信号传导。Lusvertikimab 具有抗白血病功效，具有用于 B 细胞前体急性淋巴细胞白血病 (BCP-ALL) 研究的潜力。
T39800	S2116
	S2116 is a powerful inhibitor of lysine-specific demethylase 1 (LSD1), and it is a derivative of N-alkylated tranylcypromine (TCP). S2116 exhibits its inhibitory effects by increasing H3K9 methylation and inducing reciprocal H3K27 deacetylation at super-enhancer regions. In TCP-resistant T-cell acute lymphoblastic leukemia (T-ALL) cells, S2116 triggers apoptosis by repressing the transcription of NOTCH3 and TAL1 genes. Furthermore, S2116 demonstrates significant growth retardation of T-ALL cells...
T60361	LSD1/2-IN-4
	LSD1/2-IN-4 是一种 PCPA 衍生物，是 LSD1 和 LSD2 的抑制剂。LSD1/2-IN-4 对 LSD1 和 LSD2 具有抑制作用，其Ki 值分别为 0.11 μM 和 130 μM。LSD1/2-IN-4 可用于多种癌症的研究，如 T 细胞急性淋巴细胞白血病 (TALL) 。
T74994	SJ988497	PROTACs	PROTAC
	SJ988497是一种PROTACJAK2降解剂，有效地抑制CRLF2重排(CRLF2r)细胞增殖并降解CRBN新底物GSPT1。该化合物由Ruxolitinib衍生物、连接子以及CRBN配体Pomalidomide构成，可作为急性淋巴细胞白血病(ALL)研究用途。
T35810	C24 dihydro Ceramide (d18:0/24:0) Cer(d18:0/24:0)
	C24 dihydro Ceramide is a sphingolipid that has been found in the stratum corneum of human skin.[1] It is found in higher concentrations in female sebum compared to male sebum.[2] C24 dihydro Ceramide levels positively correlate with cytotoxicity in CCRF-CEM, MOLT-4, COG-LL-317h, and COG-LL-332h T cell acute lymphoblastic leukemia (ALL) cell lines.[4] Levels of C24 dihydro ceramide are increased by 149.49-fold in dihydroceramide desaturase 1 (DEGS1) knockdown UM-SCC-22A human head and neck squam...
T83930	SJ 11646
	SJ11646是一种高效的LCK（淋巴细胞特异性蛋白酪氨酸激酶）降解剂（PROTAC；DC50= 0.00838 pM）。该化合物由Dasatinib作为LCK配体，以及基于苯基谷氨酰亚胺的cereblon结合体组成。它在体外对LCK激活的T细胞急性淋巴细胞白血病（T-ALL）细胞株和初级白血病样本展现出细胞毒性。在体内，SJ11646在源自患者的T-ALL异种移植模型中显示出抗白血病效果。
T79012	MDM2/XIAP-IN-2
	MDM2/XIAP-IN-2为MDM2（murine double minute 2）和XIAP（x-linked inhibitor of apoptosis protein）的双重抑制剂, 能够降解MDM2并抑制XIAP mRNA的翻译，进而抑制癌细胞生长。该化合物在针对急性淋巴细胞白血病细胞系EU-1的研究中显示出优秀的抑制效果，IC50值为0.3 μM。

化合物

Cat.No: T7955

Target: Apoptosis, AMPK, AChR

Cat.No: T12943

Target: Epigenetic Reader Domain, Histone Methyltransferase

Cat.No: T8308

Target: Mitochondrial Metabolism, Autophagy

Cat.No: TP1115

Synonym: L-ASNase

Target: Others

Cat.No: T16545

Synonym: Pivalyloxymethyl butyrate,AN-9

Target: Apoptosis, HDAC, Bcr-Abl

Pheniramine maleate

Cat.No: T0370

Synonym: Daneral,Inhiston,Trimetose,马来酸非尼拉敏

Target: 5-HT Receptor, Histamine Receptor

Cat.No: T1477

Synonym: NSC105823,AICA Riboside,Acadesine,阿卡地新,AICAR (Acadesine)

Target: Mitophagy, YAP, AMPK, Autophagy

Cat.No: T74710

Target: CDK, PROTACs

Cat.No: T72984

Target: Others

Cat.No: T76790

Target: Others

UNC 569 hydrochloride

Cat.No: T21302L

Synonym: UNC 569 hydrochloride (1350547-65-7 Free base)

Target: TAM Receptor, TAM Receptor

Cat.No: T36944

Target: Nucleoside Antimetabolite/Analog

Calaspargase pegol

Cat.No: T30688

Cat.No: T20858

Synonym: m-Anilinesulfonic acid,m-Sulfanilic acid

Cat.No: T24189

Synonym: J-9,J 9

Lesinurad sodium

Cat.No: T21301

Synonym: Lesinurad,RDEA 594,RDEA-594,RDEA594

HDAC3 Inhibitor

Cat.No: T36575

Erythrofuranosyladenine

Cat.No: T31672

Synonym: 9-β-D-Erythrofuranosyladenine,ETA

Cat.No: T79377

Cat.No: T78317

Synonym: Anatumomab

Cat.No: T39799

Synonym: S2157

Prexasertib mesylate

Cat.No: T4310L2

Synonym: LY-2606368,LY2606368,LY 2606368

Cat.No: T76801

Galectin-3 antagonist 2

Cat.No: T74538

Target: Galectin

Cat.No: T37068

Cat.No: T76893

Cat.No: T39800

Cat.No: T60361

Cat.No: T74994

Target: PROTACs

C24 dihydro Ceramide (d18:0/24:0)

Cat.No: T35810

Synonym: Cer(d18:0/24:0)

Cat.No: T83930

Cat.No: T79012

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