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Search Results for " vincristine "

13

抑制剂 & 化合物

4

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T38699	Piperafizine A
	Piperafizine A 是从 Streptoverticillium aspergilloides 中分离得到的，可增强 vincristine 的抗肿瘤效力。
T10991	Dehydronitrosonisoldipine	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Dehydronitrosonisoldipine 是一种不育α和含TIR 图案1的抑制剂，可用于有关神经退行性疾病的研究。Dehydronitrosonisoldipine 抑制轴突退化和长春碱激活的神经元中cADPR 的产生。
T34645	Simetride
	Simetride is used in the Reversal of resistance to vincristine in P388 leukemia.
T68209	Kopsoffinol
	Kopsoffinol is a bisindole alkaloid that has been shown to have in vitro growth inhibitory activity against human PC-3, HCT-116, MCF-7, and A549 cells and moderate effects in reversing multidrug-resistance in vincristine-resistant human KB cells.
T33510	MS-073 CP162398,CP-162398,CP 162398,MS 073
	MS-073 (CP-162398) is a P-glycoprotein inhibitor (P-gp). The in vitro resistance to vincristine (VCR) was almost completely reversed in VCR-resistant P388 cells, and the resistance of VCR, adriamycin (ADM), etoposide, and actinomycin D in ADM-resistant hu
T26413	A 30312 A-30312,A30312
	A 30312 is a fused indole, which overcomes multidrug resistance in P388/Adr cells in vitro. It potentiates the cytotoxicity of the antitumor drugs Adriamycin, vincristine and vinblastine in multidrug-resistant cells with no effect on drug-sensitive parent P388 cells.
T75642	Corydalmine hydrochloride
	Corydalmine hydrochloride 抑制某些植物病原体的孢子萌发以及腐生真菌。Corydalmine hydrochloride 具有口服活性，可用于缓解疼痛的研究。Corydalmine hydrochloride 通过抑制 NF-κB 依赖性的 CXCL1/CXCR2信号传导途径，可缓解 Vincristine 引起的神经性疼痛。
T63608	P-gp inhibitor 5
	P-gp inhibitor 5 是 P 糖蛋白 (P-gp) 的有效抑制剂，在 1.25 μM 和 2.5 μM 时 P-gp 抑制倍数分别为 2.5 和 3.0。P-gp inhibitor 5 对某些癌细胞表现出抗增殖效果。P-gp inhibitor 5 能够恢复细胞对 Vincristine 和 Paclitaxel 的敏感性，进而逆转 ABCB1/Flp-InTM-293 和 KBvin 的多药耐药 (MDR) 表型。
T64061	Mps1-IN-3 hydrochloride
	Mps1-IN-3 hydrochloride 是一种有效的、选择性的 Mps1 抑制剂 (IC50: 50 nM)。Mps1-IN-3 hydrochloride 对胶质母细胞瘤细胞的增殖表现出抑制作用，并在原位异种移植瘤模型中可有效地使胶质母细胞瘤对长春新碱敏感。
T35616	Migrastatin
	Migrastatin is a bacterial metabolite that has been found inStreptomyceswith antimuscarinic and anticancer activities.1,2It binds to M1-5muscarinic acetylcholine receptors (Kis = >200, 200, 31, 43, and >200 μM, respectively) and inhibits calcium mobilization induced by carbamoylcholine in SK-N-SH cells (IC50= 28 μM), as well as in primary rat bladder smooth muscle cells.1Migrastatin inhibits the migration of EC17 esophageal cancer cells in a wound healing assay (IC50= 10 μg/ml) and 4T1 mouse mam...
T37851	Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III)
	Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III) is an inducer of ferroptosis.1 It induces ferroptosis, but not apoptosis or necroptosis, in NB1 cancer cells when used at a concentration of 3 μM.1 Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III) inhibits proliferation of BJAB, NALM-6, Jurkat, MelHO, and MCF-7 cancer cells (IC50s = 0.07, 2.5, 1.5, 3, and 5 μM, respectively), as well as NALM-6 cells resistant to daunorubicin and vincristine when used at concentrations ranging...
T22631	Dolastatin 10 trifluoroacetate	Others	Others
	Dolastatin 10 trifluoroacetate is a potent antimitotic polypeptide isolated from a marine animal and is developed as a potential antitumor agent. Dolastatin 10 is found to have an activity to inhibit tubulin polymerization (IC50: 1.2 μM). Besides that, it
T71252	PC-046
	PC-046 is a potent tubulin-binding agent, which was originally identified for development based on selective activity in deleted in pancreas cancer locus 4 (DPC4/SMAD4) deficient tumors. PC-046 has growth inhibitory activity in a variety of tumor types in vitro, and efficacy in SCID mice was shown in human tumor xenografts of MV-4-11 acute myeloid leukemia, MM.1S multiple myeloma, and DU-145 prostate cancer. Pharmacokinetic studies demonstrated relatively high oral bioavailability (71 %) with di...

化合物

Cat.No: T38699

Dehydronitrosonisoldipine

Cat.No: T10991

Target: Calcium Channel

Cat.No: T34645

Cat.No: T68209

Cat.No: T33510

Synonym: CP162398,CP-162398,CP 162398,MS 073

Cat.No: T26413

Synonym: A-30312,A30312

Corydalmine hydrochloride

Cat.No: T75642

P-gp inhibitor 5

Cat.No: T63608

Mps1-IN-3 hydrochloride

Cat.No: T64061

Cat.No: T35616

Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III)

Cat.No: T37851

Dolastatin 10 trifluoroacetate

Cat.No: T22631

Target: Others

Cat.No: T71252

Cat. No.	Product Name	Target	Signaling Pathways
T3S0209	Vincristine	ERK; p38 MAPK; NF-κB; Akt; JNK; mTOR	Cytoskeletal Signaling; MAPK; NF-κB; PI3K/Akt/mTOR signaling
	Vincristine 与微管蛋白结合并抑制微管的形成，从而抑制癌细胞的有丝分裂。 Vincristine 可用作微管去稳定剂，用于研究治疗血液系统癌症，如白血病和淋巴瘤以及儿童肉瘤的相关研究。
T1270	Vincristine sulfate Leurocristine,22-Oxovincaleukoblastine sulfate,Leurocristine sulfate,硫酸长春新碱	Apoptosis; Microtubule Associated	Apoptosis; Cytoskeletal Signaling
	Vincristine sulfate (Leurocristine sulfate) 是一种抗肿瘤长春花生物碱。在细胞周期的 S 期不可逆地与微管(Ki: 85 nM) 和纺锤体蛋白结合，并干扰有丝分裂纺锤体的形成。
TN4962	Scholaricine	Others	Others
	Scholaricine reverses multidrug resistance in vincristine-resistant KB cells.
TN5414	Wallichinine
	Wallichinine shows inhibitory activity on platelet aggregation caused by platelet activating factor (PAF). Wallichinine with ABCB1 presents valuable clues for the development of novel MDR reversal reagents from natural products, wallichinine can significa

天然产物

Cat.No: T3S0209

Target: ERK, p38 MAPK, NF-κB, Akt, JNK, mTOR

Vincristine sulfate

Cat.No: T1270

Synonym: Leurocristine,22-Oxovincaleukoblastine sulfate,Leurocristine sulfate,硫酸长春新碱

Target: Apoptosis, Microtubule Associated

Cat.No: TN4962

Target: Others

Cat.No: TN5414

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