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adriamycin | 79549-07-8

中文名称
——
中文别名
——
英文名称
adriamycin
英文别名
Doxorubicin;Epirubicin;DOX;PLD;Triferric doxorubicin;7-(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy-6,9,11-trihydroxy-9-(2-hydroxyacetyl)-4-methoxy-8,10-dihydro-7H-tetracene-5,12-dione
adriamycin化学式
CAS
79549-07-8;129784-92-5
化学式
C27H29NO11
mdl
——
分子量
543.527
InChiKey
AOJJSUZBOXZQNB-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    39
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    206
  • 氢给体数:
    6
  • 氢受体数:
    12

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:大多数来源认为,在母亲抗肿瘤药物治疗期间,尤其是诸如阿霉素之类的环类药物,母乳喂养是禁忌的。在间歇性治疗期间,通过适当的禁乳期,可能安全地进行母乳喂养;然而,阿霉素活性代谢物阿霉素醇在乳汁中的高平及其持久性使得确定适当的禁乳间隔变得困难。有人建议在给药后禁乳5至10天,但其他数据显示,阿霉素50 mg/平方米剂量给药后,可能需要6周的时间才能使乳汁平降至安全平。 化疗可能会不利地影响母乳的正常微生物组和化学成分。在怀孕期间接受化疗的妇女更可能难以哺乳她们的婴儿。 ◉ 对哺乳婴儿的影响:一名孕妇在27周时被诊断出患有B细胞淋巴瘤。在34周零4天时诱导分娩,并在分娩后第2天开始使用标准方案的利妥昔单抗、环酰胺、阿霉素长春新碱泼尼松进行治疗,剂量不明确,每21天一个周期。她在每个周期的前10天泵奶并丢弃,用捐赠的奶喂养婴儿,然后在下一个治疗周期前的剩余10天进行母乳喂养。10天的母乳喂养禁乳期是通过使用大约3个长春新碱的半衰期来确定的。在完成4个周期的化疗后,她的婴儿据报道是健康且没有并发症地发育。 ◉ 对泌乳和母乳的影响:一项对在儿童恶性疾病中接受化疗的青少年男性的研究发现,接受过阿霉素治疗与血清催乳素浓度升高有关。 一名在怀孕第二季度被诊断为霍奇淋巴瘤的妇女在第三季度接受了3轮化疗,并在分娩后4周恢复化疗。在重新开始化疗后的16周内,收集了化疗前15至30分钟的乳汁样本。治疗方案包括每2周一次,在2小时内给予阿霉素40 mg、博来霉素16单位、长春碱9.6 mg和达卡巴嗪600 mg。她的乳汁的微生物群和代谢图谱与8名未接受化疗的健康妇女进行了比较。患者的乳汁微生物群与健康妇女明显不同,Acinetobacter sp.、Xanthomonadacae和Stenotrophomonas sp.增加,而Bifidobacterium sp.和Eubacterium sp.减少。在接受治疗的妇女的乳汁中,许多化学成分也有显著差异,尤其是DHA和肌醇减少。 对74名在怀孕的第二或第三季度在一个中心接受癌症化疗的妇女进行了电话随访研究,以确定她们产后是否成功进行母乳喂养。只有34%的妇女能够完全母乳喂养她们的婴儿,66%的妇女报告经历了母乳喂养困难。这与22名在怀孕期间被诊断但未接受化疗的母亲91%的母乳喂养成功率相比。其他具有统计学意义的相关性包括:1. 有哺乳困难的母亲平均接受了5.5个周期的化疗,而没有困难的母亲平均接受了3.8个周期;2. 有哺乳困难的母亲在怀孕期间平均提前3.4周接受了第一个周期的化疗。在接受了含有阿霉素方案治疗的62名妇女中,有39人遇到了哺乳困难。
◉ Summary of Use during Lactation:Most sources consider breastfeeding to be contraindicated during maternal antineoplastic drug therapy, especially anthracyclines such as doxorubicin. It might be possible to breastfeed safely during intermittent therapy with an appropriate period of breastfeeding abstinence; however, the high levels and persistence of the active metabolite doxorubicinol in milk make defining an appropriate abstinence interval difficult. Some have suggested a breastfeeding abstinence period of 5 to 10 days after a dose, but other data suggest that it might take 6 weeks for milk levels to drop to a safe level after a dose of doxorubicin 50 mg/sq. m. Chemotherapy may adversely affect the normal microbiome and chemical makeup of breastmilk. Women who receive chemotherapy during pregnancy are more likely to have difficulty nursing their infant. ◉ Effects in Breastfed Infants:A woman was diagnosed with B-cell lymphoma at 27 weeks of pregnancy. Labor was induced at 34 4/7 weeks and treatment was begun with a standard regimen of rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone in unspecified doses on a 21-day cycle, starting on day 2 postpartum. She pumped and discarded her milk and fed her infant donor milk for the first 10 days of each cycle and then breastfed her infant for the remaining 10 days before the next treatment cycle. The 10-day period of breastfeeding abstinence was determined by using about 3 half-lives of vincristine. After completion of 4 cycles of chemotherapy, her infant was reportedly healthy and developing without any complications. ◉ Effects on Lactation and Breastmilk:A study of adolescent males who had received chemotherapy for childhood malignancies found that having received doxorubicin was associated with elevated serum prolactin concentrations. A woman diagnosed with Hodgkin's lymphoma during the second trimester of pregnancy received 3 rounds of chemotherapy during the third trimester of pregnancy and resumed chemotherapy 4 weeks postpartum. Milk samples were collected 15 to 30 minutes before and after chemotherapy for 16 weeks after restarting. The regimen consisted of doxorubicin 40 mg, bleomycin 16 units, vinblastine 9.6 mg and dacarbazine 600 mg, all given over a 2-hour period every 2 weeks. The microbial population and metabolic profile of her milk were compared to those of 8 healthy women who were not receiving chemotherapy. The breastmilk microbial population in the patient was markedly different from that of the healthy women, with increases in Acinetobacter sp., Xanthomonadacae and Stenotrophomonas sp. and decreases in Bifidobacterium sp. and Eubacterium sp. Marked differences were also found among numerous chemical components in the breastmilk of the treated woman, most notably DHA and inositol were decreased. A telephone follow-up study was conducted on 74 women who received cancer chemotherapy at one center during the second or third trimester of pregnancy to determine if they were successful at breastfeeding postpartum. Only 34% of the women were able to exclusively breastfeed their infants, and 66% of the women reported experiencing breastfeeding difficulties. This was in comparison to a 91% breastfeeding success rate in 22 other mothers diagnosed during pregnancy, but not treated with chemotherapy. Other statistically significant correlations included: 1. mothers with breastfeeding difficulties had an average of 5.5 cycles of chemotherapy compared with 3.8 cycles among mothers who had no difficulties; and 2. mothers with breastfeeding difficulties received their first cycle of chemotherapy on average 3.4 weeks earlier in pregnancy. Of the 62 women who received a doxorubicin-containing regimen, 39 had breastfeeding difficulties.
来源:Drugs and Lactation Database (LactMed)

文献信息

  • Pharmaceutical composition comprising microbubbles for targeted tumor therapy
    申请人:Ludwig-Maximilians-Universität München
    公开号:EP2253308A1
    公开(公告)日:2010-11-24
    The present invention relates to a pharmaceutical composition for the targeted delivery of a pharmaceutically active compound, the composition comprising soft, gas-filled particles having an envelope monolayer comprising one or more surfactants and a pharmaceutically active compound. More particularly, the invention relates to a pharmaceutical composition, wherein the envelope monolayer of the gas-filled particles have a negative overall net charge, and wherein the pharmaceutically active compound has a positive overall net charge and is directly bound to one or more surfactants by both electrostatic and hydrophobic interactions. The present invention also relates to a method of producing said pharmaceutical composition comprising the steps of providing a pharmaceutical active compound- loaded liposomal preparation and the subsequent formation of gas-filled particles by adding a pharmaceutically acceptable gas to the liposomal preparation. Furthermore, the invention relates to the use of said pharmaceutical composition in the treatment of tumors.
    本发明涉及一种用于靶向输送药物活性化合物的制药组合物,该组合物包括软性气体充填颗粒,其包膜单层包括一种或多种表面活性剂和药物活性化合物。更具体地,本发明涉及一种制药组合物,其中气体充填颗粒的包膜单层具有负的总净电荷,药物活性化合物具有正的总净电荷,并且通过静电和疏相互作用直接结合在一种或多种表面活性剂上。本发明还涉及一种制备所述制药组合物的方法,包括提供药物活性化合物负载的脂质体制备和通过向脂质体制备中添加药用可接受气体形成气体充填颗粒的后续步骤。此外,本发明还涉及在肿瘤治疗中使用所述制药组合物的用途。
  • [EN] COMBINATIONS OF AKT INHIBITOR COMPOUNDS AND ABIRATERONE, AND METHODS OF USE<br/>[FR] COMBINAISONS DE COMPOSÉS INHIBITEURS D'AKT ET D'ABIRATERONE ET PROCÉDÉS D'UTILISATION
    申请人:GENENTECH INC
    公开号:WO2012135759A1
    公开(公告)日:2012-10-04
    The invention provides a combination of a) a compound of Formula (Ia): or a pharmaceutically acceptable salt thereof, and b) abiraterone or a pharmaceutically acceptable salt thereof for the prophylactic or therapeutic treatment of a hyperproliferative disorder, such as cancer.
    本发明提供了一种组合物,包括a) Formula (Ia)的化合物或其药学上可接受的盐,以及b) 阿比特龙或其药学上可接受的盐,用于预防或治疗高增殖性疾病,如癌症。
  • COMPOUNDS AND COMPOSITIONS USEFUL IN THE TREATMENT OF NEOPLASIA
    申请人:McClay Allen
    公开号:US20090047221A1
    公开(公告)日:2009-02-19
    There is described compounds for use in therapy, said compounds being defined by Formula (1): There is also described an anti-proliferative composition comprising one or more compounds according to Formula (1), and a method of treatment of neoplasia comprising the administration of such a compound or composition.
    本文描述了用于治疗的化合物,该化合物由公式(1)定义:还描述了一种抗增殖组合物,其中包括一个或多个符合公式(1)的化合物,以及一种治疗肿瘤的方法,包括给予这样的化合物或组合物。
  • MULTIFUNCTIONAL DEGRADABLE NANOPARTICLES WITH CONTROL OVER SIZE AND FUNCTIONALITIES
    申请人:Harth Eva M.
    公开号:US20090306335A1
    公开(公告)日:2009-12-10
    In one aspect, the invention relates to polymers, crosslinked polymers, functionalized polymers, nanoparticles, and functionalized nanoparticles and methods of making and using same. In one aspect, the invention relates to degradable polymer and degradable nanoparticles. In one aspect, the invention relates to methods of preparing degradable nanoparticles and, more specifically, methods of controlling particle size during the preparation of degradable nanoparticles. In one aspect, the degradable nanoparticles are useful for complexing, delivering, and releasing payloads, including pharmaceutically active payloads. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    本发明涉及聚合物、交联聚合物、功能化聚合物、纳米颗粒和功能化纳米颗粒以及其制备和使用方法。其中,本发明涉及可降解聚合物和可降解纳米颗粒。本发明还涉及制备可降解纳米颗粒的方法,更具体地说,涉及在制备可降解纳米颗粒过程中控制颗粒大小的方法。在一方面,这些可降解纳米颗粒可用于复合、传递和释放药物活性载荷等方面。本摘要旨在作为搜索特定技术领域的扫描工具,不限制本发明。
  • Multifunctional Degradable Nanoparticles with Control over Size and Functionalities
    申请人:Harth Eva M.
    公开号:US20110257343A1
    公开(公告)日:2011-10-20
    In one aspect, the invention relates to polymers, crosslinked polymers, functionalized polymers, nanoparticles, and functionalized nanoparticles and methods of making and using same. In one aspect, the invention relates to degradable polymer and degradable nanoparticles. In one aspect, the invention relates to methods of preparing degradable nanoparticles and, more specifically, methods of controlling particle size during the preparation of degradable nanoparticles. In one aspect, the degradable nanoparticles are useful for complexing, delivering, and releasing payloads, including pharmaceutically active payloads. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
    一方面,本发明涉及聚合物、交联聚合物、功能化聚合物、纳米颗粒和功能化纳米颗粒的制备和使用方法。另一方面,本发明涉及可降解聚合物和可降解纳米颗粒。另一方面,本发明涉及制备可降解纳米颗粒的方法,更具体地说,涉及在制备可降解纳米颗粒过程中控制颗粒大小的方法。另一方面,可降解纳米颗粒可用于复合、传递和释放药物活性载荷等用途。本摘要旨在作为搜索特定领域的扫描工具,不限制本发明。
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同类化合物

麻西罗霉素 领地霉素A盐酸盐 顺式-(铂-二氯(多柔比星)(叔-丁胺)) 阿霉素醇 阿霉素醇 阿霉素醇 阿霉素 阿霉素 阿雷西霉素 阿洛二霉素A 阿克那霉素B 阿克那霉素 S 阿克拉霉素 铁(3+)氯化12,17-二乙烯基-3-(3-{[3-(1H-咪唑-1-基)丙基]氨基}-3-羰基丙基)-7-(3-甲氧基-3-羰基丙基)-2,8,13,18-四甲基卟吩-21,22-二负离子(1:1:1) 道诺霉素 贝鲁比星 诺拉霉素 表阿霉素 表柔比星杂质 表柔比星EP杂质F 苯甲胺,3-[4-(1,1-二甲基乙基)苯氧基]- 美多比星 罗多比星 紫红霉素A 磷酸,2-乙基己基酯,加合2,2'-亚氨基二[乙醇] 磷酰氨基酰肼酸,2-[1-[4-[(3-氨基-2,3,6-三脱氧-a-L-来苏-六吡喃糖基)氧代]-1,2,3,4,6,11-六氢-2,5,12-三羟基-7-甲氧基-6,11-二羰基-2-萘并萘基]亚乙基]-N,N-二(2-氯乙基)-,4-溴苯基酯,盐酸盐,(2S-顺)-(9 硫霉菌素E 硫霉菌素B 硫霉菌素 盐酸阿柔比星 盐酸表柔比星 盐酸莎巴比星 盐酸氟西汀杂质 盐酸多柔比星 盐酸加柔比星 盐酸依达比星 盐酸佐柔比星 甲基N-[6-[(3-乙酰基-3,5,12-三羟基-10-甲氧基-6,11-二氧代-2,4-二氢-1H-并四苯-1-基)氧基]-3-羟基-2-甲基四氢吡喃-4-基]氨基甲酸酯 甲基7-乙酰氧基-4-({4-O-[3-O-乙酰基-2,6-二脱氧-4-O-(6-甲基-5-氧代四氢-2H-吡喃-2-基)己糖吡喃糖苷]-2,3,6-三脱氧-3-(二甲基氨基)己糖吡喃糖苷}氧基)-2-乙基-2,5,9-三羟基-6,11-二氧代-1,2,3,4,6,11-六氢-1-四c烯羧酸酯 甲基7,9-二乙酰氧基-4-({4-O-[3-O-乙酰基-2,6-二脱氧-4-O-(6-甲基-5-氧代四氢-2H-吡喃-2-基)己糖吡喃糖苷]-2,3,6-三脱氧-3-(二甲基氨基)己糖吡喃糖苷}氧基)-2-乙基-2,5-二羟基-6,11-二氧代-1,2,3,4,6,11-六氢-1-四c烯羧酸酯 甲基4-[5-[5-(4,5-二羟基-6-甲基四氢吡喃-2-基)氧基-4-羟基-6-甲基四氢吡喃-2-基]氧基-4-二甲基氨基-6-甲基四氢吡喃-2-基]氧基-2-乙基-2,5,7,10-四羟基-6,11-二氧代-3,4-二氢-1H-并四苯-1-羧酸酯 甲基4-({4-O-[3-O-乙酰基-2,6-二脱氧-4-O-(6-甲基-5-氧代四氢-2H-吡喃-2-基)己糖吡喃糖苷]-2,3,6-三脱氧-3-(二甲基氨基)己糖吡喃糖苷}氧基)-2-乙基-2,5,7,9-四羟基-6,11-二氧代-1,2,3,4,6,11-六氢-1-四c烯羧酸酯 甲基4-({4-(二甲基氨基)-5-[(2,9-二甲基-3-氧代八氢-2H,5aH-二吡喃并[2,3-b:4',3'-e][1,4]二恶英-7-基)氧基]-6-甲基四氢-2H-吡喃-2-基}氧基)-2-乙基-2,5,7,9-四羟基-6,11-二氧代-1,2,3,4,6,11-六氢-1-并四苯羧酸酯 甲基2-乙基-2,5-二羟基-6,11-二氧代-4-({2,3,6-三脱氧-4-O-[2,6-二脱氧-4-O-(6-甲基-5-氧代四氢-2H-吡喃-2-基)己糖吡喃糖苷]-3-(二甲基氨基)己糖吡喃糖苷}氧基)-1,2,3,4,6,11-六氢-1-T乙基r乙酰基烯羧酸酯 甲基(1R,2S,4S)-2,5,7-三羟基-6,11-二羰基-2-(2-羰基丙基)-4-({2,3,6-三脱氧-3-(二甲氨基)-4-O-[(2S,5S,6S)-5-{[(2S,5S,6S)-5-羟基-6-甲基四氢-2H-吡喃-2-基]氧代}-6-甲基四氢-2H-吡喃-2-基]-α-L-来苏-六吡喃糖基}氧代)-1,2,3,4,6,1 甲基(1R,2R,4S)-4-[4-二甲基氨基-5-[4-羟基-6-甲基-5-(6-甲基-5-氧代四氢吡喃-2-基)氧基四氢吡喃-2-基]氧基-6-甲基四氢吡喃-2-基]氧基-2-乙基-2,5,7,10-四羟基-6,11-二氧代-3,4-二氢-1H-并四苯-1-羧酸酯 环丁羧酸,3-(氯羰基)-2,2-二甲基-,甲基酯 烬灰红菌素X 烬灰红菌素B盐酸盐 流柔比星