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米福贝特 | 76541-72-5

中文名称
米福贝特
中文别名
(4-氯苯基)(二甲氧基膦)甲基磷酸二甲酯;米福酯
英文名称
Mifobate
英文别名
dimethyl 1-(dimethoxyphosphinyl)-1-(p-chlorophenyl)methyl phosphate;SR-202;SR202;Dimethyl α(dimethoxyphosphinyl) p-chlorobenzyl phosphate;dimethyl α-(dimethoxyphosphinyl)-p-chlorobenzylphosphate;[(4-chlorophenyl)-dimethoxyphosphorylmethyl] dimethyl phosphate
米福贝特化学式
CAS
76541-72-5
化学式
C11H17ClO7P2
mdl
MFCD00864813
分子量
358.652
InChiKey
VQHUQHAPWMNBLP-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    436.6±45.0 °C(Predicted)
  • 密度:
    1.355±0.06 g/cm3(Predicted)
  • 溶解度:
    在DMSO中的溶解度为5 毫克/毫升

计算性质

  • 辛醇/水分配系数(LogP):
    1
  • 重原子数:
    21
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.454
  • 拓扑面积:
    80.3
  • 氢给体数:
    0
  • 氢受体数:
    7

安全信息

  • 海关编码:
    2931900090
  • 危险性防范说明:
    P261,P301+P312,P302+P352,P304+P340,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335
  • 储存条件:
    -20°C,密封保存于干燥环境。

SDS

SDS:74db0cf6dff9b919d1b4dac48af34ff5
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Section 1. IDENTIFICATION OF THE SUBSTANCE/MIXTURE
Product identifiers
Product name : SR-202
CAS-No. : 76541-72-5
Relevant identified uses of the substance or mixture and uses advised against
Identified uses : Laboratory chemicals, Manufacture of substances



Section 2. HAZARDS IDENTIFICATION
Classification of the substance or mixture
Not a hazardous substance or mixture according to Regulation (EC) No 1272/2008
This substance is not classified as dangerous according to Directive 67/548/EEC.
Label elements
The product does not need to be labelled in accordance with EC directives or respective national laws.
Other hazards - none

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substances
: Dimethyl (α-dimethoxyphosphinyl-p-chlorobenzyl) phosphate
Synonyms
Mifobate
Formula : C11H17ClO7P2 C11H17ClO7P2
Molecular Weight : 358,65 g/mol

Section 4. FIRST AID MEASURES
Description of first aid measures
General advice
Consult a physician. Show this safety data sheet to the doctor in attendance.
If inhaled
If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician.
In case of skin contact
Wash off with soap and plenty of water. Consult a physician.
In case of eye contact
Flush eyes with water as a precaution.
If swallowed
Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.
Most important symptoms and effects, both acute and delayed
To the best of our knowledge, the chemical, physical, and toxicological properties have not been
thoroughly investigated.
Indication of any immediate medical attention and special treatment needed
no data available

Section 5. FIREFIGHTING MEASURES
Extinguishing media
Suitable extinguishing media
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, Oxides of phosphorus, Hydrogen chloride gas
Advice for firefighters
Wear self contained breathing apparatus for fire fighting if necessary.
Further information
no data available

Section 6. ACCIDENTAL RELEASE MEASURES
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment. Avoid dust formation. Avoid breathing vapors, mist or gas. Avoid
breathing dust.
Environmental precautions
Do not let product enter drains.
Methods and materials for containment and cleaning up
Pick up and arrange disposal without creating dust. Sweep up and shovel. Keep in suitable, closed
containers for disposal.
Reference to other sections
For disposal see section 13.

Section 7. HANDLING AND STORAGE
Precautions for safe handling
Avoid formation of dust and aerosols.
Provide appropriate exhaust ventilation at places where dust is formed.Normal measures for preventive fire
protection.
Conditions for safe storage, including any incompatibilities
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
Recommended storage temperature: -20 °C
Air sensitive. Store with desiccant.
Specific end uses
no data available

Section 8. EXPOSURE CONTROLS/PERSONAL PROTECTION
Control parameters
Components with workplace control parameters
Exposure controls
Appropriate engineering controls
Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and
at the end of workday.
Personal protective equipment
Eye/face protection
Use equipment for eye protection tested and approved under appropriate government standards
such as NIOSH (US) or EN 166(EU).
Skin protection
Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique
(without touching glove's outer surface) to avoid skin contact with this product. Dispose of
contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.
The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and
the standard EN 374 derived from it.
Body Protection
Choose body protection in relation to its type, to the concentration and amount of dangerous
substances, and to the specific work-place., The type of protective equipment must be selected
according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection
Respiratory protection is not required. Where protection from nuisance levels of dusts are desired,
use type N95 (US) or type P1 (EN 143) dust masks. Use respirators and components tested and
approved under appropriate government standards such as NIOSH (US) or CEN (EU).

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Information on basic physical and chemical properties
a) Appearance Form: crystalline
b) Odour no data available
c) Odour Threshold no data available
d) pH no data available
e) Melting point/freezing no data available
point
f) Initial boiling point and no data available
boiling range
g) Flash point no data available
h) Evaporation rate no data available
i) Flammability (solid, gas) no data available
j) Upper/lower no data available
flammability or
explosive limits
k) Vapour pressure no data available
l) Vapour density no data available
m) Relative density no data available
n) Water solubility no data available
o) Partition coefficient: n- no data available
octanol/water
p) Autoignition no data available
temperature
q) Decomposition no data available
temperature
r) Viscosity no data available
s) Explosive properties no data available
t) Oxidizing properties no data available
Other safety information
no data available

Section 10. STABILITY AND REACTIVITY
Reactivity
no data available
Chemical stability
no data available
Possibility of hazardous reactions
no data available
Conditions to avoid
no data available
Incompatible materials
Strong oxidizing agents
Hazardous decomposition products
Other decomposition products - no data available

Section 11. TOXICOLOGICAL INFORMATION
Information on toxicological effects
Acute toxicity
LD50 Oral - rat - 3.200 mg/kg
Skin corrosion/irritation
no data available
Serious eye damage/eye irritation
no data available
Respiratory or skin sensitization
no data available
Germ cell mutagenicity
no data available
Carcinogenicity
IARC: No component of this product present at levels greater than or equal to 0.1% is identified as
probable, possible or confirmed human carcinogen by IARC.
Reproductive toxicity
no data available
Specific target organ toxicity - single exposure
no data available
Specific target organ toxicity - repeated exposure
no data available
Aspiration hazard
no data available
Potential health effects
Inhalation May be harmful if inhaled. May cause respiratory tract irritation.
Ingestion May be harmful if swallowed.
Skin May be harmful if absorbed through skin. May cause skin irritation.
Eyes May cause eye irritation.
Signs and Symptoms of Exposure
To the best of our knowledge, the chemical, physical, and toxicological properties have not been
thoroughly investigated.
Additional Information
RTECS: TB8817000

Section 12. ECOLOGICAL INFORMATION
Toxicity
no data available
Persistence and degradability
no data available
Bioaccumulative potential
no data available
Mobility in soil
no data available
Results of PBT and vPvB assessment
no data available
Other adverse effects
no data available

Section 13. DISPOSAL CONSIDERATIONS
Waste treatment methods
Product
Offer surplus and non-recyclable solutions to a licensed disposal company. Contact a licensed
professional waste disposal service to dispose of this material. Dissolve or mix the material with a
combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber.
Contaminated packaging
Dispose of as unused product.

Section 14. TRANSPORT INFORMATION
UN number
ADR/RID: - IMDG: - IATA: -
UN proper shipping name
ADR/RID: Not dangerous goods
IMDG: Not dangerous goods
IATA: Not dangerous goods
Transport hazard class(es)
ADR/RID: - IMDG: - IATA: -
Packaging group
ADR/RID: - IMDG: - IATA: -
Environmental hazards
ADR/RID: no IMDG Marine pollutant: no IATA: no
Special precautions for user
no data available



SECTION 15 - REGULATORY INFORMATION
N/A


SECTION 16 - ADDITIONAL INFORMATION
N/A

制备方法与用途

生物活性

Mifobate (SR-202) 是一种有效且特异性的 PPARγ 拮抗剂,可选择性地抑制噻唑烷二酮 (TZD) 诱导的 PPARγ 转录活性 (IC50=140 μM),但不影响 PPARα、PPARβ 或 FXR 的基础或配体刺激的转录活性。这种化合物具有抗肥胖和抗糖尿病的作用。

靶点
  • PPARγ:140 μM (IC50)
体外研究

Mifobate (100-400 μM;预处理24小时) 能显著抑制 BRL 49653 和激素诱导的 3T3-L1 细胞脂肪分化,在第6天表现出剂量依赖性抑制作用。Mifobate 既能特异性地与 PPARγ 结合,又能抑制其配体依赖性的与共激活因子固醇受体共激活因子-1 (SRC-1) 的相互作用。Mifobate 还能阻断噻唑烷二酮(TZD)诱导的共激活因子 SRC-1 的招募,并且能够阻止由地塞米松、胰岛素和 3-异丁基-1 氨基黄嘌呤 (IBMX) 组合诱导的脂肪细胞分化。

体内研究

Mifobate (400 mg/kg;连续20天喂食) 能增加 ob/ob 小鼠的胰岛素敏感性。实验结果表明,这种化合物能防止血糖浓度随时间逐渐上升。实验数据如下:

  • 动物模型:8 周龄雄性 ob/ob 小鼠
  • 剂量:400 mg/kg
  • 给药方式:饲料(连续喂养20天)
  • 结果:阻止了血糖浓度随时间的上升

反应信息

  • 作为反应物:
    描述:
    1,1,1-三氟丙酮米福贝特正丁基锂 作用下, 以 四氢呋喃 为溶剂, 反应 2.25h, 以17%的产率得到1-(4-chlorophenyl)-2-trifluoromethyl-2-methylethenyl phosphate
    参考文献:
    名称:
    作为潜在杀虫剂的α-三氟亚甲基磷酸酯的设计与合成
    摘要:
    一组新的化合物,β-三氟亚甲基酚磷酸盐 [(RO)2P(O)OCRCHCF3],已通过多种方法设计和制备。其中一些表现出良好的杀虫活性。在分子结构中,设计的离去基团可以重排为强大的亲电剂,β,β-二氟乙烯基酮,这将是一种潜在的酶抑制剂。© 2003 Wiley Periodicals, Inc. 杂原子化学 14:304–308, 2003; 在线发表于 Wiley InterScience (www.interscience.wiley.com)。DOI 10.1002/hc.10147
    DOI:
    10.1002/hc.10147
  • 作为产物:
    描述:
    4-氯苯甲酰氯二乙胺 作用下, 以 乙醚 为溶剂, 反应 1.0h, 生成 米福贝特
    参考文献:
    名称:
    gem-Diphosphonate and gem-phosphonate-phosphate compounds with specific high density lipoprotein inducing activity
    摘要:
    New diphosphonate compounds and related derivatives were synthesized and investigated for their activity in specifically inducing plasma high density lipoproteins (HDL) and high density lipoprotein cholesterol (HDL-C) in normal rats. The screening of numerous compounds has permitted the determination of the structural variations leading to optimal plasma lipid altering activity, indicating antiatherosclerotic potential. Among the compounds observed to be the most active, dimethyl alpha-(dimethoxyphosphinyl)-p-chlorobenzyl phosphate (20, SR-202, mifobate) was selected for further pharmacological and subsequent clinical development.
    DOI:
    10.1021/jm00391a027
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文献信息

  • [EN] PRODRUG COMPOSITIONS AND METHODS OF TREATMENT<br/>[FR] COMPOSITIONS DE PROMÉDICAMENT ET PROCÉDÉS DE TRAITEMENT
    申请人:AQUESTIVE THERAPEUTICS INC
    公开号:WO2021087359A1
    公开(公告)日:2021-05-06
    Pharmaceutical compositions include a prodrug of epinephrine are described.
    药物组合物包括表述的肾上腺素前药。
  • Multi-functional ionic liquid compositions for overcoming polymorphism and imparting improved properties for active pharmaceutical, biological, nutritional, and energetic ingredients
    申请人:Rogers D. Robin
    公开号:US20070093462A1
    公开(公告)日:2007-04-26
    Disclosed are ionic liquids and methods of preparing ionic liquid compositions of active pharmaceutical, biological, nutritional, and energetic ingredients. Also disclosed are methods of using the compositions described herein to overcome polymorphism, overcome solubility and delivery problems, to control release rates, add functionality, enhance efficacy (synergy), and improve ease of use and manufacture.
    揭示了离子液体及制备活性药物、生物、营养和能量成分的离子液体组合物的方法。还揭示了利用本文描述的组合物的方法,以克服多型性、克服溶解度和输送问题、控制释放速率、增加功能性、增强功效(协同作用)以及改善易用性和制造工艺。
  • [EN] DUAL FUNCTIONING IONIC LIQUIDS AND SALTS THEREOF<br/>[FR] LIQUIDES IONIQUES À DOUBLE FONCTION ET SELS DE CEUX-CI
    申请人:UNIV ALABAMA
    公开号:WO2010078300A1
    公开(公告)日:2010-07-08
    Disclosed herein are ionic liquid compositions comprising active pharmaceutical, biological, and nutritional compounds, and methods of use. Further disclosed are compositions of matter including liquid ion pairs alone or in solution and their use; compositions of ionic liquids that are 'solvated,' for example, 'hydrated' and their uses.
    本文揭示了包括活性药物、生物学和营养化合物的离子液体组合物,以及其使用方法。进一步揭示了包括液态离子对的物质组合物,单独或溶解后使用;以及离子液体的“溶剂化”组合物,例如“水合”的组合物及其用途。
  • Pharmaceutical preparation comprising an active dispersed on a matrix
    申请人:——
    公开号:US20040058896A1
    公开(公告)日:2004-03-25
    The present invention relates to the field of pharmaceutical technology and describes a novel advantageous preparation for an active ingredient. The novel preparation is suitable for producing a large number of pharmaceutical dosage forms. In the new preparation an active ingredient is present essentially uniformly dispersed in an excipient matrix composed of one or more excipients selected from the group of fatty alcohol, triglyceride, partial glyceride and fatty acid ester.
    本发明涉及制药技术领域,描述了一种新的有利的活性成分制备方法。这种新的制备方法适用于生产大量的药物剂型。在这种新的制备方法中,活性成分基本上均匀地分散在由脂肪醇、甘油三酯、部分甘油酯和脂肪酸酯等多种赋形剂中选择的一种或多种赋形剂组成的赋形剂基质中。
  • Diagnostic/therapeutic agents
    申请人:Klaveness Jo
    公开号:US20050002865A1
    公开(公告)日:2005-01-06
    Targetable diagnostic and/or therapeutically active agents, e.g. ultrasound contrast agents, comprising a suspension in an aqueous carrier liquid of a reporter comprising gas-containing or gas-generating material, said agent being capable of forming at least two types of binding pairs with a target.
    可定位的诊断和/或治疗活性剂,例如超声对比剂,包括悬浮在水载体液中的报告物,该报告物包含含气体或生成气体的材料,该剂能够与目标形成至少两种结合对。
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