13
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1272L |
Cytarabine hydrochloride
Ara-C hydrochloride,Cytosine Arabinoside hydrochloride |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Cytarabine hydrochloride (Ara-C hydrochloride) 是一种核苷类似物,可导致 S 期细胞周期停滞并抑制DNA 聚合酶。Cytarabine 抑制DNA 合成,IC50为 16 nM。Cytarabine hydrochloride 对HSV 具有抗病毒作用。 | |||
T38718 |
Cytarabine triphosphate
Cytarabine triphosphate,Ara-CTP |
||
Cytarabine triphosphate (Ara-CTP), a competitive inhibitor of DNA synthesis and an active metabolite of Cytarabine, exhibits predictive potential for leukemic blasts' chemosensitivity to Cytarabine through intracellular levels. | |||
T15009 |
Elacytarabine
5'-Oleoyl cytosine arabinoside,5'-O-(Elaidoyl) 1-beta-D-arabinofuranosylcytosine,5'-Oleoyl cytarabine,艾西拉滨,CP 4055 |
Others | Others |
Elacytarabine (M7594 0037) 是核苷类似物阿糖胞苷的一种脂质缀合衍生物。Elacytarabine (M7594 0037) (CP 4055) 是一种抗肿瘤药物,在实体瘤中具有细胞毒性。 | |||
T31088 |
CPX-351
Cytarabine/daunonubicin,Vyxeos,CPX 351,Daunonubicin/cytarabine |
||
CPX-351 is a Liposomal-encapsulated combination of daunorubicin and cytarabine for the treatment of newly diagnosed tAML or AML with myelodysplasia-related changes (AML-MRCs). | |||
T29643 |
Adamantoylcytarabine
Adamantoyl cytarabine,Adam CA |
||
Adamantoylcytarabine is abioactive chemical. | |||
T15343 |
Fosteabine
YNK 01,Cytarabine ocfosfate,阿糖胞苷烷磷酯 |
Others | Others |
Fosteabine is an oral and prodrug analog of cytarabine. It is resistant to deoxycytidine deaminase. | |||
T27342L |
Flurocitabine HCl
Flurocitabine HCl(37717-21-8 Free base) |
Others | Others |
Flurocitabine HCl 是阿糖胞苷的氟化酸酐类似物,在体内部分水解成两种活性抗肿瘤物质 (阿拉伯糖基-氟尿嘧啶 (ara-FC) 和阿拉伯糖基-氟尿嘧啶 (ara-FU))。Flurocitabine HCl 在急性白血病和实体瘤的 I 期研究中具显示出抗肿瘤活性。 | |||
T79224 |
Ara-SH
|
Apoptosis | Apoptosis |
Ara-SH为Cytarabine巯基丙酸取代的衍生物,应用于通过自组装技术制造携带Cytarabine和Venetoclax的智能共负载纳米颗粒(AV-NP)的触发器。在体外和体内实验中,Ara-SH展现出显著的协同抗白血病效果。 | |||
T11956L |
MBC-11
|
Others | Others |
MBC-11 is a first-in-class conjugate of the bone-targeting bisphosphonate etidronate covalently linked to the antimetabolite cytarabine (araC). It also has the potential to treat tumor-induced bone disease (TIBD). | |||
T21161 | Ancitabine | ||
Ancitabine, a congener of cyterabine, is metabolized to cytarabine, thereby maintains a more constant antineoplastic action. | |||
T11956 |
MBC-11 triethylamine
|
Others | Others |
MBC-11 triethylamine has potential to treat tumor-induced bone disease (TIBD), is a first-in-class conjugate of the bone-targeting bisphosphonate etidronate covalently linked to the antimetabolite cytarabine (araC). | |||
T68917 |
Fazarabine
|
||
Fazarabine, also known as Kymarabine, is an orally-active pyrimidine analogue of an aza-substituted cytidine in which the ribose moiety is replaced by an arabinose sugar. Similar in action to cytarabine, fazarabine is phosphorylated by deoxycytidine kinase to a triphosphate form which competes with thymidine for incorporation into DNA; its incorporation into DNA inhibits DNA synthesis, resulting in tumor cell death and tumor necrosis. The presence of deoxycytidine kinase in a tumor is a determin... | |||
T71654 |
APcK110
|
||
APcK110 is a novel Kit inhibitor . APcK110 inhibits proliferation of the mastocytosis cell line HMC1.2 and the SCF-responsive cell line OCI/AML3 in a dose-dependent manner . APcK110 is a more potent inhibitor of OCI/AML3 proliferation than the clinically used Kit inhibitors imatinib and dasatinib and at least as potent as cytarabine. APcK110 inhibits the phosphorylation of Kit, Stat3, Stat5, and Akt in a dose-dependent fashion, showing activity of APcK110 on Kit and its downstream signaling path... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1272 |
Cytarabine
阿糖胞苷,Ara-C,Cytosine Arabinoside,Cytosine β-D-arabinofuranoside,Arabinocytidine |
Apoptosis; Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis; Endogenous Metabolite; Autophagy; HSV | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Cytarabine (Ara-C) 是一种核苷类似物,一种 DNA 合成抑制剂 (IC50=16 nM)。Cytarabine 可以抑制 DNA 聚合酶,诱导细胞周期阻滞、细胞自噬和凋亡。Cytarabine 具有抗肿瘤活性。 | |||
T1591 |
Ancitabine hydrochloride
NSC 145668 HCl,盐酸环胞苷,Cyclocytidine hydrochloride,Cyclo-CMP hydrochloride,Cyclocytidine HCl,Cyclo-C |
Others; DNA/RNA Synthesis; Autophagy | Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Others |
Ancitabine hydrochloride (NSC 145668 HCl) 是一种天然的抗白血病药物。 |