货号:A188379
同义名:
头孢唑林钠
/ Cephazolin sodium; Cefazolin sodium
Cefazolin Sodium Salt是一种β-内酰胺抗生素和第一代头孢菌素,具有杀菌活性。
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 | |||
|---|---|---|---|---|---|---|---|
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| 描述 | Cefazolin sodium is an essential drug that is widely used in clinical therapy for certain infective diseases caused by bacteria[3]. Cefazolin sodium was given intravenously before skin incision (1 g) and at the beginning of CPB (cardiopulmonary bypass) (2 g). CPB may alter the plasma protein binding and possibly distribution of cefazolin[4]. Moreover, cefazolin has a direct anti-inflammatory effect and can attenuate surgery-induced postoperative memory and learning impairment in mice[5]. Cefazolin appears similar to oxacillin for the treatment of complicated MSSA (methicillin-susceptible Staphylococcus aureus) bacteremia but with significantly improved safety[6]. Cefazolin sodium attains high serum levels and is excreted quickly via the urine. |
| Concentration | Treated Time | Description | References | |
| Mouse C8-B4 microglial cells | 250 μg/ml | 6 or 24 h | To determine the anti-inflammatory effect of cefazolin on LPS-induced inflammatory response. Results showed that cefazolin at 250 μg/ml significantly inhibited LPS-induced production of IL-6 and IL-1β. | J Neuroinflammation. 2018 Aug 22;15(1):235 |
| Administration | Dosage | Frequency | Description | References | ||
| Rats | Healthy rats | Subcutaneous injection | 100 mg/kg | Single dose | To compare the tissue distribution and plasma elimination kinetics of cefazolin, ceforanide, and cefamandole. Cefazolin had a plasma half-life of 0.5 h, plasma AUC of 184 μg·h/ml, and peak plasma concentration of 140 μg/ml. Measurable concentrations of cefazolin were found in the liver, kidneys, lungs, submaxillary glands, cervical lymph nodes, femur, heart, abdominal muscles, eyes, and testes. The tissue elimination kinetics followed the plasma elimination profiles. | Antimicrob Agents Chemother. 1981 Apr;19(4):625-7 |
| Mice | SWR/J mouse model | Oral | 0.125 g/L | Short-term 3 days or long-term 14 days | To evaluate the impact of cefazolin on the kidney microbiota in mice, results showed that cefazolin led to a loss of uroprotective Lactobacillus spp. and proliferation of Enterobacteriaceae. | Nat Commun. 2024 Dec 11;15(1):10509 |
| NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
| NCT02216227 | Surgical Site Infection | Not Applicable | Recruiting | September 30, 2019 | United States, Florida ... 展开 >> Miami VA Healthcare System, Miami, FL Recruiting Miami, Florida, United States, 33125 Contact: Gio J Baracco Lira, MD 305-575-7000 ext 4430 Gio.Baracco@va.gov Sub-Investigator: Gio J Baracco, MD United States, Iowa Iowa City VA Health Care System, Iowa City, IA Recruiting Iowa City, Iowa, United States, 52246-2208 Contact: Eli N Perencevich, MD MS BS 319-338-0581 ext 3535 eli.perencevich@va.gov Principal Investigator: Eli N. Perencevich, MD MS BS Sub-Investigator: Heather S Reisinger, PhD Sub-Investigator: Marin L. Schweizer-Looby, PhD BS Sub-Investigator: Mary S. Vaughan-Sarrazin, PhD MA United States, Maryland Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD Recruiting Baltimore, Maryland, United States, 21201 Contact: Daniel J Morgan, MD MS (410) 706-1734 Daniel.Morgan2@va.gov Sub-Investigator: Daniel Josiah Morgan, MD MS United States, Massachusetts VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA Recruiting Boston, Massachusetts, United States, 02130 Contact: Kalpana Gupta, MD MPH 857-203-5086 kalpana.gupta@va.gov Sub-Investigator: Kalpana Gupta, MD MPH United States, Michigan VA Ann Arbor Healthcare System, Ann Arbor, MI Recruiting Ann Arbor, Michigan, United States, 48105 Contact: Suzanne F Bradley, MD 734-845-3072 Suzanne.Bradley2@va.gov Sub-Investigator: Sarah L. Krein, PhD RN Sub-Investigator: Suzanne F Bradley, MD United States, Minnesota Minneapolis VA Health Care System, Minneapolis, MN Recruiting Minneapolis, Minnesota, United States, 55417 Contact: Joseph R Thurn, MD MPH 612-467-4185 seph.thurn@va.gov Sub-Investigator: Joseph R Thurn, MD MPH United States, Nebraska Omaha VA Nebraska-Western Iowa Health Care System, Omaha, NE Recruiting Omaha, Nebraska, United States, 68105-1873 Contact: Marvin J Bittner, MD 402-995-5219 Marvin.Bittner@va.gov Sub-Investigator: Marvin J Bittner, MD United States, Oregon VA Portland Health Care System, Portland, OR Recruiting Portland, Oregon, United States, 97239 Contact: Graeme N Forrest, MBBS MD 503-220-8262 ext 52118 Graeme.forrest@va.gov Sub-Investigator: Christopher D. Pfeiffer, MD MHS Sub-Investigator: Graeme N. Forrest, MBBS MD United States, Texas South Texas Health Care System, San Antonio, TX Recruiting San Antonio, Texas, United States, 78229 Contact: Jose A Cadena Zuluaga, MD 210-617-5300 Jose.Cadena-Zuluaga@va.gov Sub-Investigator: Luci Leykum, MD MBA MSc United States, Utah VA Salt Lake City Health Care System, Salt Lake City, UT Recruiting Salt Lake City, Utah, United States, 84148 Contact: Michael A Rubin, MD PhD (801) 582-1565 ext 1960 michael.rubin2@va.gov Sub-Investigator: Michael Adam Rubin, MD PhD United States, Wisconsin William S. Middleton Memorial Veterans Hospital, Madison, WI Recruiting Madison, Wisconsin, United States, 53705 Contact: Christopher J Crnich, MD PhD MS (608) 256-1901 christopher.crnich@va.gov Sub-Investigator: Christopher John Crnich, MD PhD MS 收起 << |
| NCT02225821 | Surgical Wound Infection | Phase 4 | Completed | - | Netherlands ... 展开 >> Medisch Centrum Alkmaar Alkmaar, Netherlands Flevoziekenhuis Almere, Netherlands Amstelland Ziekenhuis Amstelveen, Netherlands Academic Medical Center Amsterdam, Netherlands BovenIJ Ziekenhuis Amsterdam, Netherlands Onze Lieve Vrouwe Gasthuis Amsterdam, Netherlands Sint Lucas Andreas Ziekenhuis Amsterdam, Netherlands VU Medisch Centrum Amsterdam, Netherlands Gelre Ziekenhuizen Apeldoorn, Netherlands Rode Kruis Ziekenhuis Beverwijk, Netherlands Amphia Ziekenhuis Breda, Netherlands Reinier de Graaf Delft, Netherlands MC Haaglanden Den Haag, Netherlands Deventer Ziekenhuis Deventer, Netherlands Catharina Ziekenhuis Eindhoven, Netherlands Elkerliek Ziekenhuis Helmond, Netherlands Tergooiziekenhuizen Hilversum, Netherlands Spaarne Ziekenhuis Hoofddorp, Netherlands Westfries Gasthuis Hoorn, Netherlands Rijnland Ziekenhuis Leiderdorp, Netherlands Vlietland Ziekenhuis Schiedam, Netherlands 收起 << |
| NCT02344511 | Osteomyelitis | Phase 3 | Withdrawn | April 2019 | - |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.10mL 0.42mL 0.21mL |
10.49mL 2.10mL 1.05mL |
20.99mL 4.20mL 2.10mL |
|
| CAS号 | 27164-46-1 |
| 分子式 | C14H13N8NaO4S3 |
| 分子量 | 476.49 |
| SMILES Code | O=C([O-])C(N1[C@@]([H])([C@@H](C1=O)NC(CN2N=NN=C2)=O)SC3)=C3CSC4=NN=C(S4)C.[Na+] |
| MDL No. | MFCD00599428 |
| 别名 | 头孢唑林钠 ;Cephazolin sodium; Cefazolin sodium; SKF 41558; NSC 291561; Cefazolin (sodium salt); Ancef; cefazoline sodium |
| 运输 | 蓝冰 |
| InChI Key | FLKYBGKDCCEQQM-WYUVZMMLSA-M |
| Pubchem ID | 23675322 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, inert atmosphere, 2-8°C |
| 溶解方案 |
DMSO: 105 mg/mL(220.36 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: 100 mg/mL(209.87 mM) 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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