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BREVICON | 68-22-4

中文名称
——
中文别名
——
英文名称
BREVICON
英文别名
Micronor;17alpha-Ethinyl-19-nortestosterone;17-ethynyl-17-hydroxy-13-methyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one
BREVICON化学式
CAS
68-22-4;1670-34-4;5738-59-0;17554-51-7;19698-69-2;23944-76-5;23944-77-6;24377-25-1;32214-10-1;38673-36-8;99883-39-3;148261-68-1
化学式
C20H26O2
mdl
MFCD03265344
分子量
298.425
InChiKey
VIKNJXKGJWUCNN-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

  • 熔点:
    205-206 °C (lit.)
  • 比旋光度:
    D20 -31.7° (chloroform); D20 -25° (chloroform)
  • 沸点:
    379.83°C (rough estimate)
  • 密度:
    1.0766 (rough estimate)
  • 溶解度:
    在氯仿中的溶解度为≥50 mg/mL,澄清,无色
  • 稳定性/保质期:
    具有类似黄体酮的孕激素特性,其效果是炔孕酮的四倍,并且在抑制排卵方面比黄体酮更为显著,同时还具备轻微的雄激素和雌激素活性。

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    22
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

ADMET

毒理性
  • 在妊娠和哺乳期间的影响
◉ 母乳喂养期间使用总结:这份记录包含了关于单独使用口服炔诺孕酮作为避孕方法的具体信息。对复方口服避孕药有兴趣的人应咨询题为《避孕药,口服,复方》的记录。目前没有关于在哺乳期间使用高剂量炔诺孕酮醋酸酯的信息。 尽管在哺乳期间首选非激素方法,但像炔诺孕酮这样的仅含孕激素的避孕药被视为哺乳期选择的激素避孕药。质量较好的证据表明,炔诺孕酮不会对乳汁的成分、婴儿的生长发育或乳汁供应产生不利影响。一些证据表明,仅含孕激素的避孕药可能有助于预防哺乳期间的骨密度流失,或者至少不会加剧这种情况。计划哺乳的妇女中有很大一部分在产后3个月停止使用口服仅含孕激素的避孕药,仅含孕激素的避孕药常常导致快速再次怀孕。 ◉ 对哺乳婴儿的影响:在使用炔诺孕酮庚酸酯(Norplant)的母亲所生的婴儿中没有发现一致的身体、精神或放射学差异。一些研究发现,接受治疗的妇女的婴儿体重增长增加。 一项对12名妇女进行的研究发现,这些妇女在产后48小时开始每天口服炔诺孕酮350微克,14天内婴儿体重增长与8名服用安慰剂的妇女相比没有差异。 ◉ 对哺乳和乳汁的影响:不同规模和质量的研究表明,使用长效炔诺孕酮注射剂(醋酸酯或庚酸酯)作为避孕药,从产后6周或更晚开始使用,对乳汁质量没有重要的负面影响,对乳汁供应和哺乳期持续时间没有影响或增加。在一项研究中,产后6天接受植入物的妇女,在植入物插入后2周,观察到乳汁蛋白短暂下降。在这组妇女中,在植入物插入后2到4个月之间,也观察到乳汁磷含量的下降,在产后3个月,早期插入组的补充率更高。在另一项研究中,产后不到48小时接受炔诺孕酮庚酸酯长效注射的妇女在产后6周患产后抑郁症的可能性是非接受注射妇女的2.5到3倍。在产后1周和12周没有观察到差异。 一项对12名妇女进行的研究发现,这些妇女在产后48小时开始每天口服炔诺孕酮350微克,14天内乳汁产量和乳汁成分与8名服用安慰剂的妇女相比没有差异。 一项小型非随机研究发现,与接受非激素避孕的对照组相比,每天口服炔诺孕酮350微克会减少乳汁的数量和质量(蛋白质、脂质和钙含量降低)。 在一项非随机、非盲的研究中,比较了出院时正在哺乳的妇女,102名产后妇女在产后早期(平均51.9小时后;范围6.25至132小时)接受了甲羟孕酮醋酸酯(剂量未说明)的注射,181名妇女接受了另一种仅含孕激素的避孕药,138名妇女使用了非激素避孕药。在2周和6周时没有观察到哺乳率的差异,但在4周时使用任何激素避孕药的妇女哺乳率较低(72.1%对77.6%)。作者得出结论,在产后早期开始使用的仅含孕激素避孕药对哺乳率没有不利影响。 一项分析了一项前瞻性队列研究的数据,该研究对美国妇女进行了从2005年5月至2007年6月的研究。妇女从怀孕的第三个月开始,一直到产后第一年。分析了打算在产后3个月或更长时间哺乳的妇女中,在第三个月使用避孕药的妇女的数据(n = 1349)。打算至少哺乳4个月的妇女如果服用仅含孕激素的口服避孕药,如炔诺孕酮,那么在4个月时还在哺乳(无论是专一哺乳还是非专一哺乳)的可能性是有使用非激素避孕药妇女的3.15倍。那些说他们会哺乳3到4个月的妇女在4个月时的哺乳率与使用非激素避孕药的妇女相当。这些比率远高于那些服用含雌激素的复方口服避孕药的妇女。
◉ Summary of Use during Lactation:This record contains information specific to oral norethindrone used alone for contraception. Those with an interest in a combination oral contraceptive should consult the record entitled, Contraceptives, Oral, Combined. No information is available on the use of high-dose norethindrone acetate during breastfeeding. Although nonhormonal methods are preferred during breastfeeding, progestin-only contraceptives such as norethindrone are considered the hormonal contraceptives of choice during lactation. Fair quality evidence indicates that norethindrone does not adversely affect the composition of milk, the growth and development of the infant or the milk supply. Some evidence indicates that progestin-only contraceptives may offer protection against bone mineral density loss during lactation, or at least do not exacerbate it. A large percentage of women who planned to breastfeed discontinued oral progestin-only contraceptives by 3 months postpartum and progestin-only contraceptives often result in rapid repeat pregnancy. ◉ Effects in Breastfed Infants:No consistent physical, mental, or radiologic differences have been found in infants whose mothers were using norethindrone enanthate (Norplant). Some studies found increased infant weight gain among the infants of treated women. A short-term study of 12 women who received oral norethindrone 350 mcg daily starting 48 hours postpartum found no differences in infant weight gain over 14 days compared to 8 women taking a placebo. ◉ Effects on Lactation and Breastmilk:Studies of varying size and quality on the use of long-acting norethindrone injections (acetate or enanthate) have found that the use of levonorgestrel implants (Norplant or Norplant-2) as a contraceptive beginning at 6 weeks postpartum or later either has no clinically important negative effect on the quality of breastmilk and results in either no effect or an increase in the milk supply and duration of lactation. In one study, women who received the implant at 6 days postpartum, a transient decrease in milk protein occurred 2 weeks after implant insertion. A decrease in milk phosphorus content was also observed between 2 and 4 months after implant insertion in this group and at 3 months postpartum, the early insertion group had a higher rate of supplementation. In another study, women given norethindrone enanthate depot injection less than 48 hours postpartum were 2.5 to 3 times more likely to have postpartum depression at 6 weeks postpartum. No differences were seen at 1 and 12 weeks postpartum. A short-term study of 12 women who received oral norethindrone 350 mcg daily starting 48 hours postpartum found no differences in milk production or milk composition over 14 days compared to 8 women taking a placebo. One small, nonrandomized study found that oral norethindrone 350 mcg daily decreased the quantity and quality (lower protein, lipids and calcium) compared to controls who received nonhormonal contraception. In a nonrandomized, nonblinded study comparing women who were breastfeeding at discharge, 102 postpartum women received depot medroxyprogesterone acetate (dosage not stated) in the early postpartum period (average 51.9 hours postpartum; range 6.25 to 132 hours), 181 received another progestin-only contraceptive and 138 used nonhormonal contraception. No differences in breastfeeding rates were seen at 2 and 6 weeks, but women receiving any hormonal contraceptive were breastfeeding at a lower rate (72.1% vs 77.6%) at 4 weeks postpartum. The authors concluded that progestin-only contraception initiated in the early postpartum period had no adverse effects on breastfeeding rates. A study analyzed data from a prospective cohort study of U.S. women from May 2005 through June 2007. Women were followed from the third trimester of pregnancy throughout the first year postpartum. Data from the subset of women who intended to breastfeed for 3 months or longer postpartum during their third trimester of pregnancy and who were using a contraceptive at 3 months postpartum were analyzed (n = 1349). Women who intended to breastfeed for at least 4 months and were taking a progestin-only oral contraceptive, such as norethindrone, were 3.15 times more likely to be breastfeeding (exclusive or nonexclusive) at 4 months than women who used a nonhormonal contraceptive. Women who said they would breastfeed for 3 to 4 months had 4-month breastfeeding rates equivalent to those using a nonhormonal contraceptive. These rates were much higher than those of women who were taking an estrogen-containing, combined oral contraceptive.
来源:Drugs and Lactation Database (LactMed)

安全信息

  • 危险品标志:
    Xn
  • 安全说明:
    S22,S26,S36/37/39,S45
  • 危险类别码:
    R40
  • WGK Germany:
    3
  • 海关编码:
    2937290090
  • RTECS号:
    RC8975000
  • 危险标志:
    GHS08
  • 危险性描述:
    H351
  • 储存条件:
    本品应密封存放在阴凉干燥处,并避免光照。

SDS

SDS:022bed576f4eb3b047b21d910cb88f6a
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Section 1. Chemical Product and Company Identification
Norethindrone
Common Name/
Trade Name
Manufacturer
Commercial Name(s)
Synonym
Chemical Name
Chemical Family
Norethindrone

Section 4. First Aid Measures
Eye Contact Check for and remove any contact lenses. In case of contact, immediately flush eyes with plenty of water for at
least 15 minutes. Get medical attention if irritation occurs.
Skin Contact Wash with soap and water. Cover the irritated skin with an emollient. Get medical attention if irritation develops.
Serious Skin Contact Not available.
Inhalation If inhaled, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get
medical attention.
Serious Inhalation Not available.
Ingestion Do NOT induce vomiting unless directed to do so by medical personnel. Never give anything by mouth to an
unconscious person. Loosen tight clothing such as a collar, tie, belt or waistband. Get medical attention if
symptoms appear.
Serious Ingestion Not available.

Section 5. Fire and Explosion Data
Flammability of the Product May be combustible at high temperature.
Auto-Ignition Temperature Not available.
Flash Points Not available.
Flammable Limits Not available.
Products of Combustion Not available.
Fire Hazards in Presence of Slightly flammable to flammable in presence of heat.
Various Substances Non-flammable in presence of shocks.
Explosion Hazards in Presence Risks of explosion of the product in presence of mechanical impact: Not available.
Risks of explosion of the product in presence of static discharge: Not available.
of Various Substances
SMALL FIRE: Use DRY chemical powder.
Fire Fighting Media
and Instructions LARGE FIRE: Use water spray, fog or foam. Do not use water jet.
Not available.
Special Remarks on
Fire Hazards
Special Remarks on Explosion Not available.
Hazards

Section 6. Accidental Release Measures
Small Spill Use appropriate tools to put the spilled solid in a convenient waste disposal container. Finish cleaning by
spreading water on the contaminated surface and dispose of according to local and regional authority
requirements.
Large Spill Use a shovel to put the material into a convenient waste disposal container. Finish cleaning by spreading water
on the contaminated surface and allow to evacuate through the sanitary system.
Norethindrone

Section 7. Handling and Storage
Precautions Keep locked up.. Keep away from heat. Keep away from sources of ignition. Empty containers pose a fire risk,
evaporate the residue under a fume hood. Ground all equipment containing material. Do not ingest. Do not
breathe dust. Wear suitable protective clothing. If ingested, seek medical advice immediately and show the
container or the label. Keep away from incompatibles such as oxidizing agents.
Storage Keep container tightly closed. Keep container in a cool, well-ventilated area.

Section 8. Exposure Controls/Personal Protection
Engineering Controls Use process enclosures, local exhaust ventilation, or other engineering controls to keep airborne levels below
recommended exposure limits. If user operations generate dust, fume or mist, use ventilation to keep exposure to
airborne contaminants below the exposure limit.
Personal Protection Safety glasses. Lab coat. Dust respirator. Be sure to use an approved/certified respirator or equivalent. Gloves.
Personal Protection in Case of Splash goggles. Full suit. Dust respirator. Boots. Gloves. A self contained breathing apparatus should be used
a Large Spill to avoid inhalation of the product. Suggested protective clothing might not be sufficient; consult a specialist
BEFORE handling this product.
Exposure Limits Not available.

Section 9. Physical and Chemical Properties
Physical state and appearance Solid. (Powdered solid.) Odor Odorless.
Bitter. (Slight.)
Taste
Molecular Weight 298.4 g/mole
White.
Color
Not applicable.
pH (1% soln/water)
Boiling Point Not available.
Melting Point 204°C (399.2°F)
Critical Temperature Not available.
Specific Gravity Not available.
Not applicable.
Vapor Pressure
Vapor Density Not available.
Not available.
Volatility
Odor Threshold Not available.
Water/Oil Dist. Coeff. The product is more soluble in oil; log(oil/water) = 3
Ionicity (in Water) Not available.
Dispersion Properties See solubility in water, diethyl ether.
Solubility Partially soluble in diethyl ether.
Very slightly soluble in acetone.
Insoluble in cold water.

Section 10. Stability and Reactivity Data
Stability The product is stable.
Not available.
Instability Temperature
Conditions of Instability Excess heat, incompatible materials
Incompatibility with various Reactive with oxidizing agents.
substances
Norethindrone
Not available.
Corrosivity
Special Remarks on Not available.
Reactivity
Special Remarks on Not available.
Corrosivity
Will not occur.
Polymerization

Section 11. Toxicological Information
Routes of Entry Inhalation. Ingestion.
Toxicity to Animals Acute oral toxicity (LD50): 6000 mg/kg [Mouse].
Chronic Effects on Humans MUTAGENIC EFFECTS: Mutagenic for mammalian somatic cells.
DEVELOPMENTAL TOXICITY: Classified Reproductive system/toxin/female, Reproductive system/toxin/male
[SUSPECTED].
May cause damage to the following organs: the reproductive system.
Other Toxic Effects on Slightly hazardous in case of skin contact (irritant), of ingestion, of inhalation.
Humans
Special Remarks on Not available.
Toxicity to Animals
Special Remarks on May cause cancer.
Chronic Effects on Humans May cause adverse reproductive effects(maternal and paternal effects, effects on male and female fertility) and
birth defects.
Special Remarks on other Acute Potential Health Effects:
Toxic Effects on Humans Skin: May cause skin irritation.
Eyes: May cause eye irritation.
Inhalation: May cause respiratory tract irritation.
Ingestion: May cause gastrointestinal tract irritation. May affect endocrine system and skin (dermatitis), and
blood.

Section 12. Ecological Information
Ecotoxicity Not available.
Not available.
BOD5 and COD
Possibly hazardous short term degradation products are not likely. However, long term degradation products may
Products of Biodegradation
arise.
Toxicity of the Products Not available.
of Biodegradation
Special Remarks on the Not available.
Products of Biodegradation

Section 13. Disposal Considerations
Waste Disposal Waste must be disposed of in accordance with federal, state and local environmental
control regulations.
Norethindrone

Section 14. Transport Information
DOT Classification Not a DOT controlled material (United States).
Identification Not applicable.
Not applicable.
Special Provisions for
Transport
DOT (Pictograms)

Section 15. Other Regulatory Information and Pictograms
California prop. 65: This product contains the following ingredients for which the State of California has found to
Federal and State
cause cancer, birth defects or other reproductive harm, which would require a warning under the statute:
Regulations
Norethindrone
California prop. 65: This product contains the following ingredients for which the State of California has found to
cause birth defects which would require a warning under the statute: Norethindrone
California prop. 65: This product contains the following ingredients for which the State of California has found to
cause cancer which would require a warning under the statute: Norethindrone
Illinois toxic substances disclosure to employee act: Norethindrone
Pennsylvania RTK: Norethindrone
Minnesota: Norethindrone
Massachusetts RTK: Norethindrone
California Director's list of Hazardous Substances: Norethindrone
California California prop. 65: This product contains the following ingredients for which the State of California has found
Proposition 65 to cause cancer which would require a warning under the statute: Norethindrone
Warnings
California prop. 65: This product contains the following ingredients for which the State of California has found
to cause birth defects which would require a warning under the statute: Norethindrone
Other Regulations OSHA: Hazardous by definition of Hazard Communication Standard (29 CFR 1910.1200).
EINECS: This product is on the European Inventory of Existing Commercial Chemical Substances.
WHMIS (Canada) Not controlled under WHMIS (Canada).
Other Classifications
DSCL (EEC) R40- Possible risks of irreversible S2- Keep out of the reach of children.
effects. S36/37- Wear suitable protective clothing and
R60- May impair fertility. gloves.
S45- In case of accident or if you feel unwell,
seek medical advice immediately (show the
label where possible).
S53- Avoid exposure - obtain special
instructions before use.
Health Hazard
HMIS (U.S.A.) 1 National Fire Protection
1 Flammability
1 Association (U.S.A.)
Fire Hazard
1 0 Reactivity
Health
Reactivity
0
Specific hazard
Personal Protection
E
WHMIS (Canada)
(Pictograms)
Norethindrone
DSCL (Europe)
(Pictograms)
TDG (Canada)
(Pictograms)
ADR (Europe)
(Pictograms)
Protective Equipment
Gloves.
Lab coat.
Dust respirator. Be sure to use an
approved/certified respirator or
equivalent.


SECTION 16 - ADDITIONAL INFORMATION
N/A


制备方法与用途

药理作用

炔诺酮是19-去甲基睾酮的衍生物,是一种口服孕激素。其孕激素活性约为炔孕酮的4倍,虽然雌激素和雄激素活性较弱,但对下丘脑促黄体释放激素(LHRH)的分泌有抑制作用,通过刺激垂体前叶来降低机体对LHRH的敏感性,进而达到阻断促性腺激素释放的目的,从而产生抑制排卵的效果。口服后0.5~4小时内血药浓度可达峰值,半衰期为5~14小时,大部分代谢物经肾脏排出。

适应症

炔诺酮主要与雌激素类如炔雌醇合用作为短效口服避孕药。单独应用较大剂量时也能起到避孕效果,通过增加宫颈黏液稠度以防止精子穿透受精、抑制子宫内膜腺体发育生长影响孕卵着床等机制,适用于速效探亲避孕药。其口服容易被吸收。

剂量与用法
  • 短效口服避孕药:每次1.25~5mg,每日1~2次。
    • 包括复方炔诺酮片、膜或纸片及口服避孕片(膜)0号。从月经周期第5日开始服药,每日1片,晚饭后服用为宜(上夜班者早饭后服),连服22天,不能间断。服完等月经来后的第5日继续服药。
  • 探亲避孕药:于同居当晚开始服用,每晚1丸(5mg),同居10日内连服10丸;同居半个月内连服14丸;超过半个月者服完14丸后接着改服短效避孕药,直到探亲期结束。
  • 功能性子宫出血:每8小时服1片炔诺酮片、膜或纸片(2.5mg),紧急情况下每3小时服药一次,待流血明显减少后改为8小时一次,逐渐减量至维持量,每日1次1片,再连服20天;也可在流血停止后每天加服炔雌醇0.05mg或己烯雌酚1mg共20天。
  • 痛经、子宫内膜异位症:月经第5~7日开始,每次2.5mg,每日一次,连服20天。
不良反应

服用炔诺酮少数病人可能出现恶心、呕吐、头昏、乏力、嗜睡等类似早孕的反应,以及不规则出血、闭经、乳房胀痛、皮疹等,一般可自行消失。长期大量应用可能导致皮脂增多、痤疮或多毛现象。哺乳妇女可能引起乳汁减少,偶见突破性出血。有子宫肌瘤、高血压及肝、肾病史或乳房肿块者需慎用或禁用。

作用和用途

炔诺酮为19-去甲基睾酮衍生物,是一种强效口服孕激素,并具有轻度的雄激素和雌激素活性。它能阻断促性腺激素释放,抑制排卵,适用于口服避孕、功能性子宫出血、子宫内膜异位症、女性不育症、痛经及闭经等。

临床应用
  • 治疗功能性子宫出血:每8小时服5mg,连服3天后改为每12小时一次,7日后每次2.5~3.75mg维持2周。
  • 痛经、子宫内膜增生过度:月经第5~7日开始,每日1次,每次2.5mg,连续服用20天。
用途

孕激素类药物用于治疗月经不调、子宫功能性出血及子宫内膜异位症等。

文献信息

  • SOLUBILIZED FLAVONOID COMPOSITION
    申请人:Technology Investments LC
    公开号:EP3345594B1
    公开(公告)日:2021-11-17
  • METHODS OF INCREASING SOLUBILITY OF POORLY SOLUBLE COMPOUNDS AND METHODS OF MAKING AND USING FORMULATIONS OF SUCH COMPOUND
    申请人:API Genesis, LLC
    公开号:US20140199391A1
    公开(公告)日:2014-07-17
    The subject invention relates to novel soluble forms of planar ring structured organic compounds including flavonoids, and their production. The invention also includes the use of these novel formulations of planar ring structured organic compounds in the preparation of formulations and products. The invention also relates to a wide variety of applications of the formulations of the invention. The subject invention includes novel soluble forms and various formulations of flavonoids. Further, the invention includes novel methods of manufacturing the flavonoid formulations. The invention also relates to a wide variety of applications of the flavonoid formulations.
  • US9730953B2
    申请人:——
    公开号:US9730953B2
    公开(公告)日:2017-08-15
  • [EN] METHODS OF INCREASING SOLUBILITY OF POORLY SOLUBLE COMPOUNDS AND METHODS OF MAKING AND USING FORMULATIONS OF SUCH COMPOUNDS<br/>[FR] PROCÉDÉS VISANT À ACCROÎTRE LA SOLUBILITÉ DE COMPOSÉS FAIBLEMENT SOLUBLES, ET PROCÉDÉS DE FABRICATION ET D'UTILISATION DE FORMULATIONS DE TELS COMPOSÉS
    申请人:API GENESIS LLC
    公开号:WO2012054090A1
    公开(公告)日:2012-04-26
    The subject invention relates to novel soluble forms of planar ring structured organic compounds including flavonoids, and their production. The invention also includes the use of these novel formulations of planar ring structured organic compounds in the preparation of formulations and products. The invention also relates to a wide variety of applications of the formulations of the invention. The subject invention includes novel soluble forms and various formulations of flavonoids. Further, the invention includes novel methods of manufacturing the flavonoid formulations. The invention also relates to a wide variety of applications of the flavonoid formulations.
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