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(4R)-hydroxyochratoxin A | 35299-87-7

中文名称
——
中文别名
——
英文名称
(4R)-hydroxyochratoxin A
英文别名
4-(R)-hydroxyochratoxin;4-Hydroxyochratoxin A;(2S)-2-[[(3R,4R)-5-chloro-4,8-dihydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-7-carbonyl]amino]-3-phenylpropanoic acid
(4R)-hydroxyochratoxin A化学式
CAS
35299-87-7
化学式
C20H18ClNO7
mdl
——
分子量
419.818
InChiKey
BCZIFDALJWPHTK-YYFNMXAFSA-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):
    3.6
  • 重原子数:
    29
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    133
  • 氢给体数:
    4
  • 氢受体数:
    7

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    甲醇(4R)-hydroxyochratoxin A盐酸 作用下, 反应 24.0h, 生成 (4R)-hydroxyochratoxin A methyl ester
    参考文献:
    名称:
    Identification of ochratoxins and some of their metabolites in bile and urine of rats
    摘要:
    The objectives of this study were to develop and evaluate procedures for the confirmation of ochratoxin A (OA), lactone opened OA (OP-OA), ochratoxin B (OB), hydroxy OA (OA-OH) and ochratoxin alpha (O alpha) and metabolites formed in the rats from these toxins, and to demonstrate that many ochratoxin metabolites can he identified in the bile and urine of rats injected with the different ochratoxins. An esterification procedure in acidified methanol and a lactone hydrolysis procedure in strong base yielded two additional forms of most of the different ochratoxins. The esterification procedure provided a simple, fast and reliable method for the confirmation of the ochratoxins. A total of 20 different metabolites of OA, OP-OA, OB, OA-OH and O alpha were detected in the urine and the bile of rats of which several were identified. Among these, OA and the recently discovered and toxic form of OA (OP-OA) were readily formed in vivo when either were injected. Procedures developed in this study can be used to confirm and isolate ochratoxins in biological samples and hare shown that a new form of OA (OP-OA) along with many other metabolites are formed from OA and related ochratoxins in vivo. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0278-6915(99)00153-2
  • 作为产物:
    参考文献:
    名称:
    CASTEGNARO, MARCEL;MARU, VIBUTHI;MARU, GIRISH;RUIZ-LOPEZ, MARIA-DOLORES, ANALYST, 115,(1990) N, C. 129-131
    摘要:
    DOI:
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文献信息

  • CASTEGNARO, MARCEL;MARU, VIBUTHI;MARU, GIRISH;RUIZ-LOPEZ, MARIA-DOLORES, ANALYST, 115,(1990) N, C. 129-131
    作者:CASTEGNARO, MARCEL、MARU, VIBUTHI、MARU, GIRISH、RUIZ-LOPEZ, MARIA-DOLORES
    DOI:——
    日期:——
  • Identification of ochratoxins and some of their metabolites in bile and urine of rats
    作者:S Li、R.R Marquardt、A.A Frohlich
    DOI:10.1016/s0278-6915(99)00153-2
    日期:2000.2
    The objectives of this study were to develop and evaluate procedures for the confirmation of ochratoxin A (OA), lactone opened OA (OP-OA), ochratoxin B (OB), hydroxy OA (OA-OH) and ochratoxin alpha (O alpha) and metabolites formed in the rats from these toxins, and to demonstrate that many ochratoxin metabolites can he identified in the bile and urine of rats injected with the different ochratoxins. An esterification procedure in acidified methanol and a lactone hydrolysis procedure in strong base yielded two additional forms of most of the different ochratoxins. The esterification procedure provided a simple, fast and reliable method for the confirmation of the ochratoxins. A total of 20 different metabolites of OA, OP-OA, OB, OA-OH and O alpha were detected in the urine and the bile of rats of which several were identified. Among these, OA and the recently discovered and toxic form of OA (OP-OA) were readily formed in vivo when either were injected. Procedures developed in this study can be used to confirm and isolate ochratoxins in biological samples and hare shown that a new form of OA (OP-OA) along with many other metabolites are formed from OA and related ochratoxins in vivo. (C) 2000 Elsevier Science Ltd. All rights reserved.
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同类化合物

赭曲霉素 赭曲霉毒素A 赭曲霉毒素 C 赭曲霉毒素 A-O-甲基,甲酯 N-[(R)-3,4-二氢-8-羟基-3alpha-甲基-1-氧代-1H-2-苯并吡喃-7-基]羰基-L-苯基丙氨酸乙酯 N-[(5-氯-3,4-二氢-8-羟基-3-甲基-1-氧代-1H-2-苯并吡喃-7-基)羰基]-L-苯基丙氨酸甲酯 Ochratoxin A methyl ester tert-butyl N-((5-chloro-8-hydroxy-3-methyl-1-oxoisochroman-7-yl)carbonyl)-L-phenylalaninate 10-Hydroxyochratoxin A (4R)-hydroxyochratoxin A L-Phenylalanine, N-((5-chloro-3,4-dihydro-8-hydroxy-3-methyl-1,4-dioxo-1H-2-benzopyran-7-yl)carbonyl)-, (R)- N-((5-Chloro-8-hydroxy-3-methyl-1-oxo-7-isochromanyl)carbonyl)tyrosine Ochratoxin tc L-Phenylalanine, N-((3,4-dihydro-4,8-dihydroxy-3-methyl-1-oxo-1H-2-benzopyran-7-yl)carbonyl)-, (3R-trans)- Ochratoxin B-[d5] ochratoxin B methyl ester N-{[(3RS)-8-hydroxy-3-methyl-1-oxo-3,4-dihydro-1H-isochromen-7-yl]-carbonyl}-L-phenylalanine ochratoxin B methyl ester (S)-2-((R)-5-chloro-8-hydroxy-3-methyl-1-oxoisochroman-7-carboxamido)-3-phenylpropanoate (2R)-2-[[(3S)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-7-carbonyl]amino]-3-phenylpropanoic acid Ethyl 2-([(8-hydroxy-3-methyl-1-oxo-3,4-dihydro-1H-isochromen-7-yl)carbonyl]amino)-3-phenylpropanoate (+)-N-([(3S)-5-chloro-8-hydroxy-3-methyl-1-oxoisochroman-7-yl]carbonyl)-L phenylalanine ochratoxin A ochratoxin hydroquinone ochratoxin A 2,3,4-Trihydroxybutyl 2-[(5-chloro-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-7-carbonyl)amino]-3-phenylpropanoate ochratoxin A Methyl 2-[(5-chloro-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-7-carbonyl)amino]-3-phenylpropanoate ochratoxin B ethyl 2-[(5-chloro-8-hydroxy-3-methyl-1-oxo-3,4-dihydro-1H-2-benzopyran-7-yl)formamido]-3-phenylpropanoate 2-[(5-Chloro-4,8-dihydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-7-carbonyl)amino]-3-phenylpropanoic acid Methyl 2-[(8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-7-carbonyl)amino]-3-phenylpropanoate