37
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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。 | |||
T8003 |
Methotrexate disodium
|
Apoptosis; Dehydrogenase; DNA/RNA Synthesis; Antifolate; ADC Cytotoxin | Antibody-drug Conjugate/ADC Related; Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
Methotrexate disodium 是一种叶酸类似物代谢抑制剂,具有免疫抑制剂和抗肿瘤特性,用于类风湿关节炎和研究多种癌症。 | |||
T6603 |
Nelarabine
GW 506U78,Nelzarabine,奈拉滨,506U78 |
Apoptosis; Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Nelarabine (GW 506U78) 是一种嘌呤核苷酸类似物,为DNA 合成抑制剂,对肿瘤细胞的IC50为0.067-2.15 μM,可作用于T 细胞急性淋巴细胞白血病。 | |||
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。 | |||
T1485 |
Methotrexate
NCI-C04671,WR19039,Amethopterin,甲氨蝶呤,CL14377 |
Apoptosis; Dehydrogenase; DNA/RNA Synthesis; Antifolate; ADC Cytotoxin | Antibody-drug Conjugate/ADC Related; Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
Methotrexate (WR19039) 是一种叶酸类似物,一种二氢叶酸还原酶 DHFR 的抑制剂。Methotrexate 具有抗代谢、抗肿瘤和免疫抑制等活性,常用于类风湿关节炎和多种肿瘤的研究。 | |||
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; ADC Antibody | Antibody-drug Conjugate/ADC Related; 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。 | |||
T20858 |
Metanilic acid
m-Anilinesulfonic acid,m-Sulfanilic acid |
Others | Others |
Metanilic acid, an anti-cancer drug, is used to treat several malignancies including choriocarcinoma and pediatric acute lymphoblastic leukemia. | |||
T30688 |
Calaspargase pegol
|
Others | Others |
Calaspargase pegol is used to treat acute lymphoblastic leukemia. | |||
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。 | |||
T21301 |
Lesinurad sodium
Lesinurad,RDEA 594,RDEA-594,RDEA594 |
Others | Others |
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. | |||
T24189 |
J9
J-9,J 9 |
Others | Others |
J9 is an inhibitor of Glucocorticoid resistance. J9 reverses Dexamethasone Resistance in T-cell Acute Lymphoblastic Leukemia. | |||
T79377 |
NWP-0476
|
Others | Others |
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。 | |||
T36575 |
HDAC3 Inhibitor
|
Others | Others |
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 |
Others | Others |
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 | |||
T25000 |
Acetylaleuritolic acid
NSC 266221,NSC-266221,NSC266221 |
Others | Others |
Acetylaleuritolic acid 是一种从小花加西亚叶中分离得到的一种五环三萜类化合物,植物代谢产物。它具有抗肿瘤特性,对P-388淋巴细胞白血病测试中显示出肿瘤抑制活性。 | |||
T76801 |
Denintuzumab
|
ADC Antibody | Antibody-drug Conjugate/ADC Related |
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。 | |||
T4310L2 |
Prexasertib mesylate
LY-2606368,LY2606368,LY 2606368 |
Others | Others |
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 | |||
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 |
Others | Others |
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... | |||
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
|
Others | Others |
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. | |||
T39800 |
S2116
|
Others | Others |
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... | |||
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。 | |||
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。 | |||
T60361 |
LSD1/2-IN-4
|
Others | Others |
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) 。 | |||
T35810 |
C24 dihydro Ceramide (d18:0/24:0)
Cer(d18:0/24:0) |
Others | Others |
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... | |||
T79012 |
MDM2/XIAP-IN-2
|
Others | Others |
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。 | |||
T82259 |
Grisnilimab setaritox
WT1-RTA |
||
Grisnilimab setaritox (WT1-RTA) 是抗人 T 细胞抗体 (anti-CD7) 与蓖麻毒素 A 链 (RTA) 的结合物。RTA 是一种质量为 30 kda 的肽,能迅速活化 60S 核糖体亚基。Grisnilimab setaritox 对体外 CEM (T 淋巴母细胞白血病) 细胞具有显著细胞毒性,ID50 为 53 pM,并在恒河猴白血病性脑膜炎模型中显示出疗效改善。 | |||
T83930 |
SJ 11646
|
Others | Others |
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。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN4311 |
Isomitraphylline
|
Others | Others |
Isomitraphylline and pteropodine are the most suitable for standardization of medical cat's claw preparations. Isomitraphylline can inhibit proliferation of acute lymphoblastic leukaemia cells. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-02193 |
Tetraspanin-7/TSPAN7 Protein, Human, Recombinant (His)
Cell surface glycoprotein A15,Membrane component chromosome ... |
Human | P. pastoris (Yeast) |
May be involved in cell proliferation and cell motility. Tetraspanin-7/TSPAN7 Protein, Human, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 14.5 kDa and the accession number is P41732. | |||
TMPH-02192 |
Tetraspanin-7/TSPAN7 Protein, Human, Recombinant (E. coli, His)
Transmembrane 4 superfamily member 2,TSPAN7,Membrane compone... |
Human | E. coli |
May be involved in cell proliferation and cell motility. Tetraspanin-7/TSPAN7 Protein, Human, Recombinant (E. coli, His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 15.6 kDa and the accession number is P41732. | |||
TMPY-01850 |
CEACAM3 Protein, Human, Recombinant (His)
W282,W264,CEA,CD66D,CGM1,MGC119875,carcinoembryonic antigen ... |
Human | HEK293 Cells |
CeACAM3 (CD66d), a member of carcinoembryonic antigen family, is a granulocyte-specific receptor involved in the opsonin-independent recognition of several bacterial pathogens. There are four members in this family: CD66a, CD66b, CD66c, and CD66d. Members of CEACAM family are widely expressed especially on human neutrophils, and, depending on the tissue, capable of regulating diverse functions including tumor promotion, tumor suppression, angiogenesis, and neutrophil activation. Abnormal overexp... | |||
TMPY-02810 |
Ninjurin-1 Protein, Rat, Recombinant (hFc)
ninjurin 1 |
Rat | HEK293 Cells |
Ninjurin-1, also known as NINJ1, is a member of the Ninjurin family of transmembrane (TM) proteins. It is expressed in CD19(+) CD10(+) B-cell progenitor cells and higher levels in B-lineage acute lymphoblastic leukemia cells. Ninjurin-1 is expressed also in some other adult and embryonic tissues, predominantly in epithelial cells. Its expression is upregulated after axotomy in neurons and Schwann cells surrounding the distal nerve segment. Upregulated expression of ninjurin-1 has been identified... | |||
TMPY-05014 |
INSL6 Protein, Human, Recombinant (His)
RIF1,insulin-like 6 |
Human | HEK293 Cells |
INSL6 (Insulin-Like 6) is a Protein Coding gene. An important paralog of this gene is RLN1. The protein encoded by this gene contains a classical signature of the insulin superfamily and is significantly similar to relaxin and relaxin-like factor. INSL6 is a newly identified insulin/relaxin family peptide hormone that is predominantly expressed by the male germ cells in testes. It may have a role in sperm development and fertilization. A recent murine study demonstrated that INSL6-knockout resul... |