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N-[6-[(10aR)-6,6,9-trimethyl-6a,7,10,10a-tetrahydrobenzo[c]chromen-3-yl]hex-4-ynyl]methanesulfonamide

中文名称
——
中文别名
——
英文名称
N-[6-[(10aR)-6,6,9-trimethyl-6a,7,10,10a-tetrahydrobenzo[c]chromen-3-yl]hex-4-ynyl]methanesulfonamide
英文别名
——
N-[6-[(10aR)-6,6,9-trimethyl-6a,7,10,10a-tetrahydrobenzo[c]chromen-3-yl]hex-4-ynyl]methanesulfonamide化学式
CAS
——
化学式
C23H31NO3S
mdl
——
分子量
401.6
InChiKey
OPZOTPYRVKZPDO-BGERDNNASA-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):
    4.1
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    63.8
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • USE OF CANNABINOID COMPOUNDS FOR STIMULATING MELANOGENESIS
    申请人:Zuccolo Michela
    公开号:US20140193349A1
    公开(公告)日:2014-07-10
    The invention relates to the nontherapeutic cosmetic use of at least one cannabinoid compound chosen from the compounds corresponding to general formula (I): and also the geometric isomers and optical isomers thereof, the cosmetically acceptable acid or base salts thereof, and the hydrates thereof; in which compounds of formula (I): R 1 represents a hydrogen atom or a C 1 -C 30 alkyl group; it being possible for said alkyl group to be optionally substituted with a hydroxyl (OH) group; R 2 represents a halogen atom or a group chosen from hydroxyl, thiol (SH), and amino optionally substituted with one or two C 1 -C 6 alkyl groups; R 3 and R 4 form, together with the carbon atom which bears them, an oxo group or else R 3 and R 4 represent a hydrogen atom; R 5 represents a hydrogen atom or a C 1 -C 6 alkyl group; X represents a heteroatom chosen from oxygen and sulfur atoms and the divalent group —N(R 6 )—, with R 6 representing a hydrogen atom or a C 1 -C 6 alkyl group; represents a single or double bond; n is 1, 2 or 3, preferentially 1 or 2; it being understood that, when R 3 and R 4 together form an oxo group with the carbon atom which bears them and X represents an oxygen atom, then R 1 cannot represent a hydroxymethyl group, as an agent for coloring keratin materials. It also relates to one of these specific cannabinoid compounds for use thereof in the treatment of vitiligo or pityriasis versicolor, to nontherapeutic cosmetic processes for coloring the skin or for treating canities, comprising the topical application to the skin and/or head hair, or the oral administration, of a composition comprising, in a physiologically acceptable medium, one of these cannabinoid compounds, and to a process for selecting an active agent which promotes the pigmentation of keratin materials.
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