货号:A667625
同义名:
链脲佐菌素
/ NSC-85998; SZN
Streptozotocin (Streptozocin) 是一种广泛用于实验动物中诱导糖尿病的抗生素。Streptozotocin 通过葡萄糖转运蛋白 (GLUT2) 进入 β 细胞并导致 DNA 烷基化,从而引起 β 细胞凋亡。
HazMat Fee + There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
| Type | HazMat fee for 500 gram (Estimated) |
| Excepted Quantity | USD 0.00 |
| Limited Quantity | USD 15-60 |
| Inaccessible (Haz class 6.1), Domestic | USD 80+ |
| Inaccessible (Haz class 6.1), International | USD 150+ |
| Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
| Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
| {[ item.pr_size ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} | 现货 | 1周 咨询 | - + |
快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解

| 描述 | The alkylation of DNA by carcinogens such as the alkyl nitrosoureas is a critical event in the induction of tumors by these compounds. Streptozotocin, an antibiotic widely used for induction of diabetes in experimental animals and for the treatment of pancreatic neoplasms, was shown to be a potent methylating agent reacting with DNA in vitro to form methylated purines. Rats received streptozotocin (21 mg/kg; 2 mCi/kg) by i.v. injection for 2 hours before death. The liver was alkylated to the greatest extent followed by the kidney. In both of these organs, the degree of methylation was significantly greater than that observed with N-methyl-N-nitrosourea. While methylation of brain DNA by streptozotocin was very low, suggesting that the compound does not penetrate well into the nervous system[3]. Male C57BL/6 mice were under inhalation anesthesia injected via the penile vein with streptozocin (180 mg/kg). Treated mice showed elevated blood glucose levels 48 h after drug injection and reduced body weight significantly compared with control group. Streptozocin also significantly attenuated the numbers of splenocytes and white blood cells (WBC) at 96 h post injection[4]. |
| Concentration | Treated Time | Description | References | |
| LLC-PK1 cells | 10 mM | 24 hours and 72 hours | To evaluate the protective effect of IOEs on STZ-induced renal tubular cell injury, results showed that EtCE-EA increased cell survival at both 24 and 72 hours. | Int J Mol Sci. 2023 Feb 23;24(5):4443. |
| Administration | Dosage | Frequency | Description | References | ||
| Mice | 3xTg-AD mice | Intracerebroventricular injection | 3.0 mg/kg | Single injection, lasting 3-6 weeks | To investigate the effects of STZ on cognitive function and Alzheimer-like brain abnormalities in 3xTg-AD mice. Results showed that STZ exacerbated impairment of short-term and spatial reference memory, increased tau hyperphosphorylation and neuroinflammation, disturbed brain insulin signaling, and decreased synaptic plasticity and amyloid β peptides in the brain. | Mol Neurobiol. 2014 Feb;49(1):547-62 |
| Rats | Streptozotocin-induced type 1 diabetes model | Intraperitoneal injection | 50 mg/kg | Single injection | The study aimed to investigate the therapeutic effects of hDPSCs transplantation on parotid gland injury in a rat model of STZ-induced type 1 diabetes. Results showed that hDPSCs transplantation decreased blood glucose, improved parotid gland weight and salivary flow rate, reduced oxidative stress, and promoted parotid cell regeneration. | Stem Cell Res Ther. 2021 Nov 14;12(1):577 |
| Sprague-Dawley rats | Streptozotocin-induced diabetic rat model | Intraperitoneal injection | 60 mg/kg | Single injection | To investigate the effect of glycemic variability on peripheral nerve damage in streptozotocin-induced diabetic rats. The results suggest that glucose control itself is more important than glucose fluctuation in preventing peripheral nerve damage. | Diabetes Metab J. 2022 Jan;46(1):117-128 |
| Mice | 1/3 NT + STZ-induced diabetic nephropathy model | Intraperitoneal injection | 75 mg/kg and 100 mg/kg | Once a week for 7 days | To evaluate the protective effect of EtCE-EA on diabetic nephropathy, results showed that EtCE-EA effectively improved renal function indicators and reduced renal damage. | Int J Mol Sci. 2023 Feb 23;24(5):4443. |
| C57BL/6J mice | Streptozotocin-induced diabetes model | Intraperitoneal injection | Single high dose 150 mg/kg or multiple low doses 50 mg/kg | Single high dose administered once, multiple low doses administered over 5 consecutive days | To study the effects of streptozotocin on pancreatic β-cells and observe the progression of hyperglycemia and diabetes | Sci Data. 2022 Sep 10;9(1):558 |
| Mice | Diet-induced obesity and low-dose streptozotocin-induced hyperglycemia model | Intraperitoneal injection | 50 mg/kg | Five consecutive days | To evaluate the effect of GPR39 deletion on post-ischemic revascularization in hyperglycemic mice. Results showed that GPR39 deletion significantly accelerated blood perfusion recovery and reduced tissue necrosis in hyperglycemic mice. | Proc Natl Acad Sci U S A. 2023 Jan 3;120(1):e2208541120 |
| Mice | Model of maternal diabetes-induced NTDs | Intravenous injection in the tail vein | 75 mg/kg | For 2 consecutive days | To study the effect of PKCα on neural tube defects under diabetic pregnancy conditions, results showed PKCα activation leads to autophagy impairment and neural tube defects | Nat Commun. 2017 May 5;8:15182 |
| Mice | Type-1 diabetic mouse model | Intraperitoneal injection | 50 mg/kg body weight | Six consecutive injections, maintained for 32 weeks | To study the effect of L-Anserine nitrate on kidney fibrosis in a type-1 diabetic mouse model. Results showed that Cndp1-KO mice had significantly increased kidney anserine and carnosine concentrations, reduced glycative and oxidative stress in the kidney, and mitigated interstitial inflammation and fibrosis. | Antioxidants (Basel). 2023 Jun 14;12(6):1270 |
| Animal study | 糖尿病[5] 动物:C57BL/6 小鼠,雌雄皆可,10周龄。 给药:200 mg/kg ,腹腔注射 ,单次高剂量 |
| NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
| NCT01362530 | Chemotherapy Induced Nausea an... 展开 >>d Vomiting 收起 << | Phase 3 | Completed | - | - |
| NCT01362530 | - | Completed | - | - | |
| NCT00003543 | Colorectal Cancer | Phase 1 | Completed | - | United States, New York ... 展开 >> Memorial Sloan-Kettering Cancer Center New York, New York, United States, 10021 收起 << |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
3.77mL 0.75mL 0.38mL |
18.85mL 3.77mL 1.89mL |
37.70mL 7.54mL 3.77mL |
|
| CAS号 | 18883-66-4 |
| 分子式 | C8H15N3O7 |
| 分子量 | 265.22 |
| SMILES Code | O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](NC(N(C)N=O)=O)[C@H]1O |
| MDL No. | MFCD00006607 |
| 别名 | 链脲佐菌素 ;NSC-85998; SZN; SZC; NRRL 2697; AI3-50821; NCI-C03167; NSC 37917; Estreptozocin; STZ; U 9889 |
| 运输 | 蓝冰 |
| InChI Key | ZSJLQEPLLKMAKR-GKHCUFPYSA-N |
| Pubchem ID | 29327 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, store in freezer, under -20°C |
| 溶解方案 |
DMSO: 250 mg/mL(942.61 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO H2O: 110 mg/mL(414.75 mM)
|
沪公网安备 31011702889066号
沪ICP备2024050318号-1