3-hydrazinobenzyl alcohol | 143445-58-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 3-hydrazinobenzyl alcohol
• 英文别名: m-(Hydroxymethyl)phenylhydrazine；(3-hydrazinylphenyl)methanol
• CAS: 143445-58-3
• 化学式: C₇H₁₀N₂O
• mdl: MFCD09999862
• 分子量: 138.169
• InChiKey: KVJJRXXOXCJIJO-UHFFFAOYSA-N

物化性质

• 熔点：
  268 °C
• 沸点：
  334.8±25.0 °C(Predicted)
• 密度：
  1.257±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  10
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.142
• 拓扑面积：
  58.3
• 氢给体数：
  3
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-hydrazinobenzyl alcohol 在 新戊醇 、 偶氮二甲酸二异丙酯 、 硫酸 、 三苯基膦 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 为溶剂， 反应 31.25h， 生成 1-[(1',3',3'-Trimethyl-6-nitrospiro[chromene-2,2'-indole]-6'-yl)methyl]pyrrole-2,5-dione
  参考文献：
  名称：

  Family of Site-Selective Molecular Optical Switches

  摘要：

  [GRAPHIVS]We describe the design, synthesis, and characterization of a family of thiol-reactive optical switches for labeling proteins and other biomolecules. Site-selective introduction of photochromic probes within biomolecules is being used as part of a new approach for optical control of biomolecular interactions and activities within cells. The thiol-reactive photochromic probes described in this report include a spironaplithoxazine and five spirobenzopyrans. The location of the thiol-reactive group on the spirobenzopyran is different for each probe; this feature can be used to control the geometry of the optical switch within a bioconjugate. The photochromes undergo rapid and reversible, optically driven transitions between a colorless spiro (SP) state and a brightly colored merocyanine (MC) state. The MC absorption of a spironaphthoxazine conjugate is red shifted by more than 100 nm compared to the equivalent spirobenzopyran, which may be exploited for the independent control of the MC to SP transition for up to two different spironaphthoxazine and spirobenzopyran conjugates within the same sample.

  DOI：

  10.1021/jo048207o
• 作为产物：
  描述：

  3-氨基苯甲醇 在 盐酸 、 sodium nitrite 、 tin(ll) chloride 、 sodium hydroxide 作用下， 以 水 为溶剂， 反应 1.0h， 生成 3-hydrazinobenzyl alcohol
  参考文献：
  名称：

  PHOTOCHROMIC PROBES

  摘要：

  本发明提供了如权利要求1所示的光致变色化合物及其衍生物，以及这些化合物和衍生物的使用方法。本发明还提供了能够在第一状态和第二状态之间进行光导向可逆转换的光致变色光学探针。该发明还教授了确定和控制可逆光学生物分子相互作用的方法，例如在受试者中钙结合的方法。

  公开号：

  US20070195309A1

文献信息

• PHOTOCHROMIC PROBES
  申请人：MARRIOTT J. D. Gerard

  公开号：US20070195309A1

  公开（公告）日：2007-08-23

  The present invention provides photochromic compounds and derivatives thereof as shown in claim 1 and methods of use of these compounds and derivatives. The present invention also provides photochromic optical probes capable of undergoing light directed reversible transition between a first state and a second state. The invention also teaches methods of determining and controlling reversible optical biomolecular interactions, for example binding of calcium in a subject.

  本发明提供了如权利要求1所示的光致变色化合物及其衍生物，以及这些化合物和衍生物的使用方法。本发明还提供了能够在第一状态和第二状态之间进行光导向可逆转换的光致变色光学探针。该发明还教授了确定和控制可逆光学生物分子相互作用的方法，例如在受试者中钙结合的方法。
• KINASE INHIBITORS
  申请人：RESPIVERT LIMITED

  公开号：US20150210722A1

  公开（公告）日：2015-07-30

  There are provided compounds of formula (I), wherein R 1 to R 5 , X 1 , X 2 , Ar, L, A, A 1 , E and G have meanings given in the description, which compounds have anti-inflammatory activity (e.g., through inhibition of one or more of members of: the family of p38 mitogen-activated protein kinase enzymes; Syk kinase; and members of the Src family of tyrosine kinases) and have use in therapy, including in pharmaceutical combinations, especially in the treatment of inflammatory diseases, including inflammatory diseases of the lung, eye and intestines.

  提供了化合物的结构式(I)，其中R1至R5，X1，X2，Ar，L，A，A1，E和G的含义如描述所示，这些化合物具有抗炎活性（例如，通过抑制p38丝裂原活化蛋白激酶家族中的一个或多个成员；Syk激酶；以及酪氨酸激酶Src家族的成员之一）并且可用于治疗，包括在药物组合中，尤其是用于治疗包括肺部、眼部和肠道炎症疾病在内的炎症性疾病。
• Functionalized pyrazoles and pyrazolo[3,4-d]pyridazinones: Synthesis and evaluation of their phosphodiesterase 4 inhibitory activity
  作者：Pierfrancesco Biagini、Claudio Biancalani、Alessia Graziano、Nicoletta Cesari、Maria Paola Giovannoni、Agostino Cilibrizzi、Vittorio Dal Piaz、Claudia Vergelli、Letizia Crocetti、Maurizio Delcanale、Elisabetta Armani、Andrea Rizzi、Paola Puccini、Paola Maria Gallo、Daniele Spinabelli、Paola Caruso

  DOI：10.1016/j.bmc.2010.03.066

  日期：2010.5

  A series of pyrazoles and pyrazolo[3,4-d]pyridazinones were synthesized and evaluated for their PDE4 inhibitory activity. All the pyrazoles were found devoid of activity, whereas some of the novel pyrazolo[3,4-d]pyridazinones showed good activity as PDE4 inhibitors. The most potent compounds in this series showed an IC50 in the nanomolar range. The ability to inhibit TNF-alpha release in human PBMCs was determined for two representative compounds, finding values in the sub-micromolar range. SARs studies demonstrated that the best arranged groups around the heterocyclic core are 2-chloro-, 2-methyl- and 3-nitrophenyl at position 2, an ethyl ester at position 4 and a small alkyl group at position 6. Molecular modeling studies performed on a representative compound allowed to define its binding mode to the PDE4B isoform. (C) 2010 Elsevier Ltd. All rights reserved.
• Alkali-metal cation recognition induced isomerization of spirobenzopyrans and spironaphthoxazins possessing a crown ring as a recognition site: multifunctional artificial receptors
  作者：Masahiko Inouye、Masaru Ueno、Kikuo Tsuchiya、Naomi Nakayama、Takashi Konishi、Teijiro Kitao

  DOI：10.1021/jo00046a019

  日期：1992.9

  Spirobenzopyrans and spironaphthoxazins possessing a monoaza-crown ring were synthesized. Isomerization of these compounds to the open colored merocyanines was induced by recognition of alkali-metal cations and the selectivity of the coloration was found to be governed by several factors: (1) the size of the crown ring, (2) the position of recognition, (3) electric properties of both the complexed cations and the merocyanine dipoles, and (4) the length of the alkyl chains connecting the spirobenzopyran units and the crown units. The spirobenzopyrans represent rationally designed multifunctional artificial receptors for alkali-metal cations.
• US4158007A
  申请人：——

  公开号：US4158007A

  公开（公告）日：1979-06-12