製品番号: HY-N0488

硫酸ビンクリスチン

(別名: Vincristine sulfate; Leurocristine sulfate; NSC-67574 sulfate; 22-Oxovincaleukoblastine sulfate)

75 Cited Publications

カスタマーレビュー

Based on 75 publication(s) in Google Scholar

Vincristine (Leurocristine; NSC-67574; 22-Oxovincaleukoblastine) sulfate is a microtubule inhibitor that disrupts microtubule polymerization by binding to β-tubulin (with a K_i of 85 nM in bovine), arrests the cell cycle and induces apoptosis. Vincristine sulfate inhibits cell replication, tumor blood flow and the proliferation of various cancer cells, while triggering effects such as oxidative stress, inflammation, calcium overload, epithelial-mesenchymal transition and peripheral neuropathic pain. Vincristine sulfate upregulates the expression of various transporters and nuclear receptors, and enriches gastric cancer stem-like cells. Vincristine sulfate is used in research related to various tumors including acute lymphoblastic leukemia, lymphoma, melanoma, gastric cancer, solid tumors and sarcomas.

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純度: 99.43%
CAS 番号: 2068-78-2
分子式: C₄₆H₅₈N₄O₁₄S
分子量:923.04

保管条件:

4°C, sealed storage, away from moisture and light

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

Vincristine sulfate 構造式

CAS 番号: 2068-78-2

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生物活性
- 製品説明
- Cellular Effect
- 体外実験
- 体内実験
化学情報
Publications (75)
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純度とドキュメンテーション
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生物活性

製品説明

Cellular Effect

Cell Line	Type	Value	Description	References
A 172	IC₅₀	>100 μM Compound: Vincristine	Cytotoxic activity against human tumor A-172 cell line Cytotoxic activity against human tumor A-172 cell line	[PMID: 15857148]
A549	IC₅₀	171.5 nM Compound: Vincristine sulphate	Antiproliferative activity against human A549 cells after 48 hrs by MTT assay Antiproliferative activity against human A549 cells after 48 hrs by MTT assay	[PMID: 28038323]
A549	IC₅₀	20 nM Compound: Vincristine sulfate	Cytotoxicity against human A549 cells after 72 hrs by alamar blue assay Cytotoxicity against human A549 cells after 72 hrs by alamar blue assay	[PMID: 23215348]
ARO	IC₅₀	<0.0001 μM Compound: Vincristine	Cytotoxic activity against human tumor Aro cell line Cytotoxic activity against human tumor Aro cell line	[PMID: 15857148]
BT-549	IC₅₀	54.72 nM Compound: Vincristine sulphate	Antiproliferative activity against human BT549 cells after 48 hrs by MTT assay Antiproliferative activity against human BT549 cells after 48 hrs by MTT assay	[PMID: 28038323]
Cancer cell lines	GI₅₀	0.1 μM Compound: Vincristine sulfate	Growth inhibition of human CNS cancer cell by NCI-CLS assay Growth inhibition of human CNS cancer cell by NCI-CLS assay	[PMID: 20395150]
Cancer cell lines	GI₅₀	0.1 μM Compound: Vincristine sulfate	Growth inhibition of human colon cancer cell by NCI-CLS assay Growth inhibition of human colon cancer cell by NCI-CLS assay	[PMID: 20395150]
Cancer cell lines	GI₅₀	0.1 μM Compound: Vincristine sulfate	Growth inhibition of human prostate cancer cell by NCI-CLS assay Growth inhibition of human prostate cancer cell by NCI-CLS assay	[PMID: 20395150]
Cancer cell lines	GI₅₀	0.1 μM Compound: vincristine sulfate	Growth inhibition of human colon cancer cells after 48 hrs Growth inhibition of human colon cancer cells after 48 hrs	[PMID: 20684599]
Cancer cell lines	GI₅₀	0.1 μM Compound: Vincristine sulfate	Cytotoxicity against human colon cancer cells after 48 hrs Cytotoxicity against human colon cancer cells after 48 hrs	[PMID: 24747749]
Cancer cell lines	GI₅₀	0.13 μM Compound: vincristine sulfate	Growth inhibition of human CNS cancer cells after 48 hrs Growth inhibition of human CNS cancer cells after 48 hrs	[PMID: 20684599]
Cancer cell lines	GI₅₀	0.13 μM Compound: vincristine sulfate	Growth inhibition of human prostate cancer cells after 48 hrs Growth inhibition of human prostate cancer cells after 48 hrs	[PMID: 20684599]
Cancer cell lines	GI₅₀	0.13 μM Compound: vincristine sulfate	Cytotoxicity against human CNS cancer cells after 48 hrs Cytotoxicity against human CNS cancer cells after 48 hrs	[PMID: 22283430]
Cancer cell lines	GI₅₀	0.13 μM Compound: vincristine sulfate	Cytotoxicity against human prostate cancer cells after 48 hrs Cytotoxicity against human prostate cancer cells after 48 hrs	[PMID: 22283430]
Cancer cell lines	GI₅₀	0.13 μM Compound: Vincristine sulfate	Cytotoxicity against human CNS cancer cells after 48 hrs Cytotoxicity against human CNS cancer cells after 48 hrs	[PMID: 24747749]
Cancer cell lines	GI₅₀	0.13 μM Compound: Vincristine sulfate	Cytotoxicity against human prostate cancer cells after 48 hrs Cytotoxicity against human prostate cancer cells after 48 hrs	[PMID: 24747749]
Cancer cell lines	GI₅₀	0.3 μM Compound: Vincristine sulfate	Growth inhibition of human breast cancer cell by NCI-CLS assay Growth inhibition of human breast cancer cell by NCI-CLS assay	[PMID: 20395150]
Cancer cell lines	GI₅₀	0.3 μM Compound: Vincristine sulfate	Growth inhibition of human ovarian cancer cell by NCI-CLS assay Growth inhibition of human ovarian cancer cell by NCI-CLS assay	[PMID: 20395150]
Cancer cell lines	GI₅₀	0.3 μM Compound: Vincristine sulfate	Growth inhibition of human renal cancer cell by NCI-CLS assay Growth inhibition of human renal cancer cell by NCI-CLS assay	[PMID: 20395150]
Cancer cell lines	GI₅₀	0.32 μM Compound: vincristine sulfate	Growth inhibition of human breast cancer cells after 48 hrs Growth inhibition of human breast cancer cells after 48 hrs	[PMID: 20684599]
Cancer cell lines	GI₅₀	0.32 μM Compound: vincristine sulfate	Growth inhibition of human Ovarian cancer cells after 48 hrs Growth inhibition of human Ovarian cancer cells after 48 hrs	[PMID: 20684599]
Cancer cell lines	GI₅₀	0.32 μM Compound: vincristine sulfate	Growth inhibition of human renal cancer cells after 48 hrs Growth inhibition of human renal cancer cells after 48 hrs	[PMID: 20684599]
Cancer cell lines	GI₅₀	0.32 μM Compound: vincristine sulfate	Cytotoxicity against human breast cancer cells after 48 hrs Cytotoxicity against human breast cancer cells after 48 hrs	[PMID: 22283430]
Cancer cell lines	GI₅₀	0.32 μM Compound: vincristine sulfate	Cytotoxicity against human ovarian cancer cells after 48 hrs Cytotoxicity against human ovarian cancer cells after 48 hrs	[PMID: 22283430]
Cancer cell lines	GI₅₀	0.32 μM Compound: vincristine sulfate	Cytotoxicity against human renal cancer cells after 48 hrs Cytotoxicity against human renal cancer cells after 48 hrs	[PMID: 22283430]
Cancer cell lines	GI₅₀	0.32 μM Compound: Vincristine sulfate	Cytotoxicity against human breast cancer cells after 48 hrs Cytotoxicity against human breast cancer cells after 48 hrs	[PMID: 24747749]
Cancer cell lines	GI₅₀	0.32 μM Compound: Vincristine sulfate	Cytotoxicity against human ovarian cancer cells after 48 hrs Cytotoxicity against human ovarian cancer cells after 48 hrs	[PMID: 24747749]
Cancer cell lines	GI₅₀	0.32 μM Compound: Vincristine sulfate	Cytotoxicity against human renal cancer cells after 48 hrs Cytotoxicity against human renal cancer cells after 48 hrs	[PMID: 24747749]
DU-145	IC₅₀	71.83 μM Compound: Vincristine sulphate	Cytotoxicity against human DU145 cells assessed as inhibition of cell viability after 48 hrs by MTT assay Cytotoxicity against human DU145 cells assessed as inhibition of cell viability after 48 hrs by MTT assay	[PMID: 29174816]
DU-145	IC₅₀	72.3 nM Compound: Vincristine sulphate	Antiproliferative activity against human DU145 cells after 48 hrs by MTT assay Antiproliferative activity against human DU145 cells after 48 hrs by MTT assay	[PMID: 28038323]
HEK293	IC₅₀	31 nM Compound: Vincristine sulfate	Cytotoxicity against human HEK cells after 72 hrs by alamar blue assay Cytotoxicity against human HEK cells after 72 hrs by alamar blue assay	[PMID: 23215348]
HeLa	IC₅₀	0.0358 μM Compound: Vincristine sulfate	Cytotoxicity against human HeLa cells assessed as inhibition of cell viability after 72 hrs by alamar blue assay Cytotoxicity against human HeLa cells assessed as inhibition of cell viability after 72 hrs by alamar blue assay	[PMID: 23489291]
HeLa	IC₅₀	36 nM Compound: Vincristine sulfate	Cytotoxicity against human HeLa cells after 72 hrs by alamar blue assay Cytotoxicity against human HeLa cells after 72 hrs by alamar blue assay	[PMID: 23215348]
HepG2	IC₅₀	0.1 μM Compound: Vincristine	Cytotoxic activity against human tumor Hep G2 cell line Cytotoxic activity against human tumor Hep G2 cell line	[PMID: 15857148]
HepG2	IC₅₀	0.69 μM Compound: 2; VCR.H2SO4	Cytotoxicity against human HepG2 cells after 72 hrs by SRB assay Cytotoxicity against human HepG2 cells after 72 hrs by SRB assay	[PMID: 26522953]
HL-60	IC₅₀	11.2 μg/mL Compound: vincristine sulfate	Cytotoxicity against human HL60 cells after 48 hrs Cytotoxicity against human HL60 cells after 48 hrs	[PMID: 17432904]
HT-29	IC₅₀	0.1 μM Compound: Vincristine	Cytotoxic activity against human tumor HT-29 cell line Cytotoxic activity against human tumor HT-29 cell line	[PMID: 15857148]
IGROV-1	IC₅₀	0.01 μM Compound: Vincristine	Cytotoxic activity against human tumor Igrov-1 cell line Cytotoxic activity against human tumor Igrov-1 cell line	[PMID: 15857148]
KB	IC₅₀	0.02 μM Compound: 2; VCR.H2SO4	Cytotoxicity against human KB cells after 72 hrs by SRB assay Cytotoxicity against human KB cells after 72 hrs by SRB assay	[PMID: 26522953]
L02	IC₅₀	28.4 μg/mL Compound: vincristine sulfate	Cytotoxicity against human L02 cells after 48 hrs Cytotoxicity against human L02 cells after 48 hrs	[PMID: 17432904]
Leukemia cell	GI₅₀	0.1 μM Compound: Vincristine sulfate	Growth inhibition of human leukemia cell by NCI-CLS assay Growth inhibition of human leukemia cell by NCI-CLS assay	[PMID: 20395150]
Leukemia cell	GI₅₀	0.1 μM Compound: vincristine sulfate	Growth inhibition of human leukemia cells after 48 hrs Growth inhibition of human leukemia cells after 48 hrs	[PMID: 20684599]
Leukemia cell	GI₅₀	0.1 μM Compound: vincristine sulfate	Cytotoxicity against human leukemia cells after 48 hrs Cytotoxicity against human leukemia cells after 48 hrs	[PMID: 22283430]
Leukemia cell	GI₅₀	0.1 μM Compound: Vincristine sulfate	Cytotoxicity against human leukemia cells after 48 hrs Cytotoxicity against human leukemia cells after 48 hrs	[PMID: 24747749]
LNCaP	IC₅₀	0.0029 μM Compound: Vincristine sulphate	Cytotoxicity against human LNCAP cells after 72 hrs by alamar blue assay Cytotoxicity against human LNCAP cells after 72 hrs by alamar blue assay	[PMID: 20732809]
LNCaP	IC₅₀	6.1 nM Compound: Vincristine sulfate	Cytotoxicity against human LNCAP cells after 72 hrs by alamar blue assay Cytotoxicity against human LNCAP cells after 72 hrs by alamar blue assay	[PMID: 23215348]
Lu1	IC₅₀	0.48 μM Compound: 2; VCR.H2SO4	Cytotoxicity against human Lu1 cells after 72 hrs by SRB assay Cytotoxicity against human Lu1 cells after 72 hrs by SRB assay	[PMID: 26522953]
MCF7	IC₅₀	0.01 μM Compound: Vincristine	Cytotoxic activity against human tumor MCF-7 cell line Cytotoxic activity against human tumor MCF-7 cell line	[PMID: 15857148]
MCF7	IC₅₀	0.51 μM Compound: 2; VCR.H2SO4	Cytotoxicity against human MCF7 cells after 72 hrs by SRB assay Cytotoxicity against human MCF7 cells after 72 hrs by SRB assay	[PMID: 26522953]
MDA-MB-231	IC₅₀	116.6 nM Compound: Vincristine sulphate	Antiproliferative activity against human MDA-MB-231 cells after 48 hrs by MTT assay Antiproliferative activity against human MDA-MB-231 cells after 48 hrs by MTT assay	[PMID: 28038323]
Melanoma cell	GI₅₀	0.16 μM Compound: vincristine sulfate	Growth inhibition of human melanoma cells after 48 hrs Growth inhibition of human melanoma cells after 48 hrs	[PMID: 20684599]
Melanoma cell	GI₅₀	0.16 μM Compound: vincristine sulfate	Cytotoxicity against human melanoma cells after 48 hrs Cytotoxicity against human melanoma cells after 48 hrs	[PMID: 22283430]
Melanoma cell	GI₅₀	0.16 μM Compound: Vincristine sulfate	Cytotoxicity against human melanoma cells after 48 hrs Cytotoxicity against human melanoma cells after 48 hrs	[PMID: 24747749]
Melanoma cell	GI₅₀	0.2 μM Compound: Vincristine sulfate	Growth inhibition of human melanoma cell by NCI-CLS assay Growth inhibition of human melanoma cell by NCI-CLS assay	[PMID: 20395150]
NFF	IC₅₀	0.0169 μM Compound: Vincristine sulfate	Cytotoxicity against human NFF cells assessed as inhibition of cell viability after 72 hrs by alamar blue assay Cytotoxicity against human NFF cells assessed as inhibition of cell viability after 72 hrs by alamar blue assay	[PMID: 23489291]
NFF	IC₅₀	17 nM Compound: Vincristine sulfate	Cytotoxicity against human NFF cells after 72 hrs by alamar blue assay Cytotoxicity against human NFF cells after 72 hrs by alamar blue assay	[PMID: 23215348]
NSCLC	GI₅₀	0.2 μM Compound: Vincristine sulfate	Growth inhibition of human NSCLC cell by NCI-CLS assay Growth inhibition of human NSCLC cell by NCI-CLS assay	[PMID: 20395150]
NSCLC	GI₅₀	0.25 μM Compound: vincristine sulfate	Growth inhibition of human NSCLC cells after 48 hrs Growth inhibition of human NSCLC cells after 48 hrs	[PMID: 20684599]
NSCLC	GI₅₀	0.25 μM Compound: vincristine sulfate	Cytotoxicity against human NSCLC cells after 48 hrs Cytotoxicity against human NSCLC cells after 48 hrs	[PMID: 22283430]
NSCLC	GI₅₀	0.25 μM Compound: Vincristine sulfate	Cytotoxicity against human NSCLC cells after 48 hrs Cytotoxicity against human NSCLC cells after 48 hrs	[PMID: 24747749]
OVCAR-3	IC₅₀	0.01 μM Compound: Vincristine	Cytotoxic activity against human tumor Ovcar-3 cell line Cytotoxic activity against human tumor Ovcar-3 cell line	[PMID: 15857148]
PC-3	IC₅₀	0.011 μM Compound: Vincristine sulphate	Cytotoxicity against human PC3 cells after 72 hrs by alamar blue assay Cytotoxicity against human PC3 cells after 72 hrs by alamar blue assay	[PMID: 20732809]
PC-3	IC₅₀	0.0153 μM Compound: Vincristine sulfate	Cytotoxicity against human PC3 cells assessed as inhibition of cell viability after 72 hrs by alamar blue assay Cytotoxicity against human PC3 cells assessed as inhibition of cell viability after 72 hrs by alamar blue assay	[PMID: 23489291]
PC-3	IC₅₀	15 nM Compound: Vincristine sulfate	Cytotoxicity against human PC3 cells after 72 hrs by alamar blue assay Cytotoxicity against human PC3 cells after 72 hrs by alamar blue assay	[PMID: 23215348]
PC-3	IC₅₀	27.6 nM Compound: Vincristine sulphate	Antiproliferative activity against human PC3 cells after 48 hrs by MTT assay Antiproliferative activity against human PC3 cells after 48 hrs by MTT assay	[PMID: 28038323]
PC-3	IC₅₀	28.11 μM Compound: Vincristine sulphate	Cytotoxicity against human PC3 cells assessed as inhibition of cell viability after 48 hrs by MTT assay Cytotoxicity against human PC3 cells assessed as inhibition of cell viability after 48 hrs by MTT assay	[PMID: 29174816]
SMMC-7721	IC₅₀	26.7 μg/mL Compound: vincristine sulfate	Cytotoxicity against human SMMC7721 cells after 48 hrs Cytotoxicity against human SMMC7721 cells after 48 hrs	[PMID: 17432904]

体外実験

Vincristine sulfate (100 nM; 0-48 h) induces apoptosis in G1-phase enriched ALL-2 and ALL-5 cells without mitotic arrest (no MPM2 staining); it also induces apoptosis in G2-M phase enriched ALL-2 and ALL-5 cells in the presence of mitotic arrest (enhanced MPM2 staining)^[2].
Acute treatment with Vincristine sulfate (1 μM; 2 h) inhibits the proliferation of B16 melanoma cells, and its potency is lower than that of vinblastine (HY-13780) and vindesine (HY-16514)^[4].
Vincristine sulfate (5-2000 nM; 24-48 h) induces mRNA expression of ABCC2, ABCC3, PXR and CYP3A4 (10 nM, 48 h) in LS174T and A549 cells, and regulates the expression of ABCB1 and ABCC2 in Caco2 cells in a concentration- and time-dependent manner^[5].
Treatment of SGC7901 cells with Vincristine sulfate (0.5-1.5 μg/mL) upregulates the mRNA expression of Snail, Twist, MRP and Pgp, indicating that the epithelial-mesenchymal transition and multidrug resistance pathways are activated^[6].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

体内実験

Vincristine (5-10 mg/kg; i.v.) sulfate induces significant tumor necrosis and reduces tumor blood flow in mice subcutaneously implanted with colon 38 adenocarcinoma^[3].
Vincristine (10 mg/kg; i.p.) sulfate induces significant tumor necrosis in subcutaneous multidrug-resistant P388 leukemia subline xenografts in mice^[3].
Vincristine (75 μg/kg; i.p.; daily; 10 days) sulfate induces peripheral neuropathic pain in mice, which is characterized by behavioral, electrophysiological, histopathological, oxidative stress and inflammatory changes^[7].
Vincristine (0.1 mg/kg; i.p.; daily; 7 days) sulfate induces dose- and duration-dependent peripheral neuropathic pain and oxidative stress in mice^[8].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

化学情報

CAS 番号 2068-78-2
性状 Solid
分子量 923.04
分子式 C₄₆H₅₈N₄O₁₄S
Color White to off-white
SMILES

CC[C@@]1(C=CCN2CC3)[C@@]2([H])[C@@]3(C4=CC([C@](C5=C6C7=CC=CC=C7N5)(C[C@](C[C@](CC)(O)C8)([H])C[N@@]8CC6)C(OC)=O)=C(OC)C=C4N9C=O)[C@]9([H])[C@](C(OC)=O)(O)[C@@H]1OC(C)=O.O=S(O)(O)=O
別名

Vincristine sulfate; Leurocristine sulfate; NSC-67574 sulfate; 22-Oxovincaleukoblastine sulfate
Structure Classification
- Alkaloids
- Alkaloid Dimers
Initial Source
輸送条件

Room temperature in continental US; may vary elsewhere.
保管条件

4°C, sealed storage, away from moisture and light

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

Publications (75)

All IFCell Proliferation/Viability AssayApoptosis AnalysisWB

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Journal Impact Factor

Nature

Catabolism of extracellular glutathione supplies cysteine to support tumours. [Abstract]

2026 May;653(8115):933-941. PMID: 41851454
Cell

SARM1 senses dsDNA to promote NAD+ degradation and cell death. [Abstract]

2025 Dec 11;188(25):7137-7154.e21. PMID: 41138726

Vincristine sulfate purchased from MedChemExpress. Usage Cited in: Cell. 2025 Dec 11;188(25):7137-7154.e21. [Abstract]

Representative IF images showing the colocalization between mSARM1 and the noted chemo-induced cytosolic dsDNA in neural cells. The noted neural cells were treated with 20 μM CP, 100 μM CBP, or 0.5 μM VCR (Vincristine) for 36 h, followed by IF analyses. Green: dsDNA stained with anti-dsDNA antibody; red: mSARM1 stained with anti-SARM1 antibody; blue: DAPI. Scale bar, 10 μm.
Cell

Cancer SLC6A6-mediated taurine uptake transactivates immune checkpoint genes and induces exhaustion in CD8+ T cells. [Abstract]

2024 Apr 25;187(9):2288-2304.e27. PMID: 38565142
Mol Cancer

Organoids derived from patients provide a new opportunity for research and individualized treatment of malignant peritoneal mesothelioma. [Abstract]

2024 Jan 10;23(1):12. PMID: 38200517
Cancer Commun (Lond)

N6-methyladenosine reader hnRNPA2B1 recognizes and stabilizes NEAT1 to confer chemoresistance in gastric cancer. [Abstract]

2024 Apr;44(4):469-490. PMID: 38512764

Vincristine sulfate purchased from MedChemExpress. Usage Cited in: Cancer Commun (Lond). 2024 Apr;44(4):469-490. [Abstract]

IC₅₀ values of SGC7901^VCR shNC and SGC7901^VCR shA2B1 cells treated with VCR (Vincristine, 0.1-100 µg/mL; 48 h) and 5‐Fu (0.1-100 µg/mL; 48 h).

Vincristine sulfate purchased from MedChemExpress. Usage Cited in: Cancer Commun (Lond). 2024 Apr;44(4):469-490. [Abstract]

Apoptosis of SGC7901^VCRshNC and SGC7901^VCR shA2B1 cells treated with VCR (Vincristine, 1 or 15 µg/mL; 48 h) and 5‐Fu (1 or 20 µg/mL; 48 h).
Drug Resist Updat

Replacing the tropolonic methoxyl group of colchicine with methylamino increases tubulin binding affinity with improved therapeutic index and overcomes paclitaxel cross-resistance. [Abstract]

2023 Feb 13;68:100951. PMID: 36841134
Cell Mol Immunol

Arsenic trioxide elicits prophylactic and therapeutic immune responses against solid tumors by inducing necroptosis and ferroptosis. [Abstract]

2023 Jan;20(1):51-64. PMID: 36447031

Vincristine sulfate purchased from MedChemExpress. Usage Cited in: Cell Mol Immunol. 2023 Jan;20(1):51-64. [Abstract]

Comparison of drug (Epirubicin hydrochloride, EPI; Daunorubicin hydrochloride, DNR; Vinorelbine ditartrate, VNR; Oxaliplatin, OXA; Vincristine, VCR; Artemisinin, ART; Colchicine, COL) cytotoxicity to TC1 cells at the indicated doses and time points measured with CCK-8 assays. R.U. (Relative unit) was calculated from the average O.D. values in each condition as the indicator of cell viability (n = 3).
Nat Commun

RAS/MEK/PI3K pathway inhibition augments response to CD40 agonism by targeting CD11b+ Bregs thereby overcoming melanoma PD1-resistance. [Abstract]

2026 Jan 12;17(1):162. PMID: 41526341
J Clin Invest

DNA topoisomerase II inhibition potentiates osimertinib's therapeutic efficacy in EGFR-mutant non-small cell lung cancer models. [Abstract]

2024 Mar 7;134(10):e172716. PMID: 38451729

Vincristine sulfate purchased from MedChemExpress. Usage Cited in: J Clin Invest. 2024 Mar 7;134(10):e172716. [Abstract]

The given cell lines were treated with 250 nM osimertinib (Osim), 1.25 μM Etoposide (VP-16), 125 nM Doxorubicin (DXR), 5 nM Paclitaxel, 10 μM Cisplatin, 25 μM Carboplatin, 25 nM Gemcitabine, 20 nM 5-Fluorouracil (5-FU), 25 μM Cyclophosphamide, 25 μM Capecitabine, or 10 nM Vincristine alone or in combination for 3 days. Cell numbers were then measured using the SRB assay.
Leukemia

Downregulation of MTSS1 in acute myeloid leukemia is associated with a poor prognosis, chemotherapy resistance, and disease aggressiveness. [Abstract]

2021 Oct;35(10):2827-2839. PMID: 33782537

Vincristine sulfate purchased from MedChemExpress. Usage Cited in: Leukemia. 2021 Oct;35(10):2827-2839. [Abstract]

TF-1 derivative cell lines were incubated with the indicated concentrations of vincristine (20 nM) or Regorafenib (10 μM) for 2 days, and the proportions of apoptotic cells were determined by staining with AnnexinV. Mean + SEM, n = 3.
Sci Adv

Single-cell profiling of alveolar rhabdomyosarcoma reveals RAS pathway inhibitors as cell-fate hijackers with therapeutic relevance. [Abstract]

2023 Feb 10;9(6):eade9238. PMID: 36753540
Mol Ther

Exosomal miR-1246 from glioma patient body fluids drives the differentiation and activation of myeloid-derived suppressor cells. [Abstract]

2021 Dec 1;29(12):3449-3464. PMID: 34217892
MedComm (2020)

KSQ-4279, an Inhibitor of Ubiquitin Specific Peptidase 1, Enhanced the Chemotherapeutic Efficacy in ABCB1/ABCG2/ABCC1-Mediated Multidrug Resistant Cancers. [Abstract]

2025 Nov 29;6(12):e70517. PMID: 41328326
Cell Rep Med

Single-cell profiles delineate immune cell remodeling and enhanced tumor-fibroblast interaction of hepatoblastoma after chemotherapy. [Abstract]

2025 Oct 21;6(10):102401. PMID: 41038160
Cell Rep Med

scRNA-seq reveals an immune microenvironment and JUN-mediated NK cell exhaustion in relapsed T-ALL. [Abstract]

2025 Apr 25:102098. PMID: 40306275
Cell Rep Med

CAN-Scan: A multi-omic phenotype-driven precision oncology platform identifies prognostic biomarkers of therapy response for colorectal cancer. [Abstract]

2025 Apr 2:102053. PMID: 40187357
Cell Rep Med

Histone lysine demethylase 4 family proteins maintain the transcriptional program and adrenergic cellular state of MYCN-amplified neuroblastoma. [Abstract]

2024 Mar 19;5(3):101468. PMID: 38508144
Pharmacol Res

Time-dependent proteomics and drug response in expanding cancer cells. [Abstract]

2024 May 9:204:107208. PMID: 38729587
Cell Death Dis

Both direct and indirect suppression of MCL1 synergizes with BCLXL inhibition in preclinical models of gastric cancer. [Abstract]

2025 Mar 12;16(1):170. PMID: 40075071
Proc Natl Acad Sci U S A

Selective inhibitors of SARM1 targeting an allosteric cysteine in the autoregulatory ARM domain. [Abstract]

2022 Aug 30;119(35):e2208457119. PMID: 35994671
Cell Commun Signal

BI-2865, a pan-KRAS inhibitor, reverses the P-glycoprotein induced multidrug resistance in vitro and in vivo. [Abstract]

2024 Jun 13;22(1):325. PMID: 38872211
Int J Biol Macromol

Ribophorin II potentiates P-glycoprotein- and ABCG2-mediated multidrug resistance via activating ERK pathway in gastric cancer. [Abstract]

2019 May 1:128:574-582. PMID: 30710584

Vincristine sulfate purchased from MedChemExpress. Usage Cited in: Int J Biol Macromol. 2019 May 1:128:574-582. [Abstract]

SGC7901/DDP or SGC7901/VCR (Vincristine) cells are transfected with si-Con or si-ERK, and transfection efficiency is evaluated by western blot assay at 48 h post transfection.
Acta Pharmacol Sin

A novel FAK-degrading PROTAC molecule exhibited both anti-tumor activities and efficient MDR reversal effects. [Abstract]

2024 Oct;45(10):2174-2185. PMID: 38844788
Acta Pharmacol Sin

Osimertinib successfully combats EGFR-negative glioblastoma cells by inhibiting the MAPK pathway. [Abstract]

2021 Jan;42(1):108-114. PMID: 32398685
Cancer Immunol Res

Discovery of podofilox as a potent cGAMP-STING signaling enhancer with antitumor activity. [Abstract]

2023 May 3;11(5):583-599. PMID: 36921097
J Transl Med

Papillary thyroid cancer organoids harboring BRAFV600E mutation reveal potentially beneficial effects of BRAF inhibitor-based combination therapies. [Abstract]

2023 Jan 9;21(1):9. PMID: 36624452
Biomed Pharmacother

Mitoquinone alleviates vincristine-induced neuropathic pain through inhibiting oxidative stress and apoptosis via the improvement of mitochondrial dysfunction. [Abstract]

2020 May;125:110003. PMID: 32187955
PLoS Biol

A high-throughput behavioral screening platform for measuring chemotaxis by C. elegans. [Abstract]

2024 Jun 27;22(6):e3002672. PMID: 38935621
Cell Chem Biol

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溶剤 & 溶解度

体外:

DMSO : 350 mg/mL (379.18 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

H₂O : 50 mg/mL (54.17 mM; Need ultrasonic)

View the Complete Stock Solution Preparation Table

Preparing Stock Solutions

View the Complete Stock Solution Preparation Table

Concentration Solvent Mass

1 mg

5 mg

10 mg

Concentration

Solvent

Mass

1 mM

1.0834 mL

5.4169 mL

10.8338 mL

5 mM

0.2167 mL

1.0834 mL

2.1668 mL

10 mM

0.1083 mL

0.5417 mL

1.0834 mL

Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.

Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

モル濃度計算機

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass

濃度

体積

分子量

希釈計算機

濃度 _(開始) × 体積 _(開始) = 濃度 _(終了) × 体積 _(終了)

濃度 _(開始)

体積 _(開始)

濃度 _(終了)

体積 _(終了)

体内:

Select the appropriate dissolution method based on your experimental animal and administration route.

Stock Solution Working Solution

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline

Solubility: ≥ 4.17 mg/mL (4.52 mM); Clear solution

This protocol yields a clear solution of ≥ 4.17 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (41.7 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

Protocol 2

Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)

Solubility: ≥ 4.17 mg/mL (4.52 mM); Clear solution

This protocol yields a clear solution of ≥ 4.17 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (41.7 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

Protocol 3

Add each solvent one by one: 10% DMSO 90% Corn Oil

Solubility: ≥ 4.17 mg/mL (4.52 mM); Clear solution

This protocol yields a clear solution of ≥ 4.17 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (41.7 mg/mL) to 900 μL Corn oil, and mix evenly.

Working Solution

For the following dissolution methods, please prepare the working solution directly:

It is recommended to prepare fresh solutions and use them promptly within a short period of time.

The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: PBS

Solubility: 100 mg/mL (108.34 mM); Clear solution; Need ultrasonic and warming and heat to 60°C

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage
mg/kg
Animal Weight (Per Animal)
g
Dosing Volume (Per Animal)
μL
Number of Animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Working solution concentration: 0.22 mg/mL

This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.

The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact

MedChemExpress (MCE) .

プロトコル

Cell Assay^[1]

Cells are plated in 2 mL of medium in 35 mm plates at a concentration of about 5×10⁴ cells/mL and grow for 24 h at 37°C in an atmosphere of 5% CO₂ and 95% air. Then medium is replaced with fresh medium lacking or containing 4 nM drug and proliferation is continued for 3 days. Cell counts are done each day in a Coulter Counter after detaching the cells with trypsin and EDTA.

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

純度とドキュメンテーション

バッチを選択:

純度: 99.98%

Assay: 99.98%

ee.: 99.98%

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COA (2659 KB)
元素分析報告書 (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
取扱説明書 (2659 KB)

参考文献

[1]. Douer D, et al. Efficacy and Safety of Vincristine Sulfate Liposome Injection in the Treatment of Adult Acute Lymphocytic Leukemia. Oncologist. 2016;21(7):840-847. [Content Brief]

[2]. Kothari A, et al. Cell Cycle-Dependent Mechanisms Underlie Vincristine-Induced Death of Primary Acute Lymphoblastic Leukemia Cells. Cancer Res. 2016;76(12):3553-3561. [Content Brief]

[3]. Baguley BC, et al. Inhibition of growth of colon 38 adenocarcinoma by vinblastine and colchicine: evidence for a vascular mechanism. Eur J Cancer. 1991;27(4):482-487. [Content Brief]

[4]. Jordan MA, et al. Comparison of the effects of vinblastine, vincristine, vindesine, and vinepidine on microtubule dynamics and cell proliferation in vitro. Cancer Res. 1985;45(6):2741-2747. [Content Brief]

[5]. Huang R, et al. Vincristine transcriptional regulation of efflux drug transporters in carcinoma cell lines. Biochem Pharmacol. 2006;71(12):1695-1704. [Content Brief]

[6]. Xue Z, et al. Identification of cancer stem cells in vincristine preconditioned SGC7901 gastric cancer cell line. J Cell Biochem. 2012;113(1):302-312. [Content Brief]

[7]. Gong SS, et al. Neuroprotective Effect of Matrine in Mouse Model of Vincristine-Induced Neuropathic Pain. Neurochem Res. 2016;41(11):3147-3159. [Content Brief]

[8]. Babu A, et al. Effect of curcumin in mice model of vincristine-induced neuropathy. Pharm Biol. 2015;53(6):838-848. [Content Brief]

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
H₂O / DMSO	1 mM	1.0834 mL	5.4169 mL	10.8338 mL	27.0844 mL
	5 mM	0.2167 mL	1.0834 mL	2.1668 mL	5.4169 mL
	10 mM	0.1083 mL	0.5417 mL	1.0834 mL	2.7084 mL
	15 mM	0.0722 mL	0.3611 mL	0.7223 mL	1.8056 mL
	20 mM	0.0542 mL	0.2708 mL	0.5417 mL	1.3542 mL
	25 mM	0.0433 mL	0.2167 mL	0.4334 mL	1.0834 mL
	30 mM	0.0361 mL	0.1806 mL	0.3611 mL	0.9028 mL
	40 mM	0.0271 mL	0.1354 mL	0.2708 mL	0.6771 mL
	50 mM	0.0217 mL	0.1083 mL	0.2167 mL	0.5417 mL
DMSO	60 mM	0.0181 mL	0.0903 mL	0.1806 mL	0.4514 mL
	80 mM	0.0135 mL	0.0677 mL	0.1354 mL	0.3386 mL
	100 mM	0.0108 mL	0.0542 mL	0.1083 mL	0.2708 mL

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

Keywords

Vincristine sulfate

75 Cited Publications

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MedChemExpress（MCE）の使用を引用している文献 Vincristine sulfate

生物活性

化学情報

Publications (75)

溶剤 & 溶解度

プロトコル

純度とドキュメンテーション

参考文献

Help & FAQs

Complete Stock Solution Preparation Table

Vincristine sulfate 関連分類

製品番号: HY-N0488