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ICG | 13010-66-7

中文名称
——
中文别名
——
英文名称
ICG
英文别名
indocyanine green;4-[(2Z)-2-[7-[1,1-dimethyl-3-(4-sulfobutyl)benzo[e]indol-3-ium-2-yl]hepta-2,4,6-trienylidene]-1,1-dimethylbenzo[e]indol-3-yl]butane-1-sulfonic acid
ICG化学式
CAS
13010-66-7
化学式
C43H49N2O6S2
mdl
——
分子量
754.004
InChiKey
BDBMLMBYCXNVMC-UHFFFAOYSA-O
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):
    8.6
  • 重原子数:
    53
  • 可旋转键数:
    14
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    132
  • 氢给体数:
    2
  • 氢受体数:
    7

ADMET

毒理性
  • 蛋白质结合
百分之九十八
98%
来源:DrugBank
吸收、分配和排泄
  • 吸收
它在约800纳米处有一个峰值光谱吸收。
It has a peak spectral absorption at about 800 nm.
来源:DrugBank
吸收、分配和排泄
  • 消除途径
染料以未结合形式通过胆汁排出。
The dye is excreted in bile in unconjugated form.
来源:DrugBank
吸收、分配和排泄
  • 分布容积
ICG分布到小鼠胎儿中时,当与OATP或P-糖蛋白抑制剂同时使用时,可以增强。在单个胎儿组织内更大的分布可能与ICG更大的跨胎盘转移有关。
ICG distribution into the mouse fetus can be enhanced when used concomitantly with OATP or P-glycoprotein inhibitors. The greater distribution within individual fetal tissues is likely related to ICG's greater transplacental transfer.
来源:DrugBank
吸收、分配和排泄
  • 清除
清除主要经由肝脏从循环系统中移除的染料是评估肝脏功能的最佳方法之一。
Clearance of dyes which are removed from the circulation principally by the liver constitutes one of the best methods for evaluating hepatic function.
来源:DrugBank

反应信息

  • 作为反应物:
    描述:
    十八胺ICG三聚氯氰三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 0.5h, 以56%的产率得到
    参考文献:
    名称:
    NANOPARTICLE COATED WITH LIGAND INTRODUCED WITH LONG HYDROPHOBIC CHAIN AND METHOD FOR PREPARING SAME
    摘要:
    本发明涉及一种纳米颗粒,其具有连接到长链烷基或烯基的连接剂,以及制备该纳米颗粒的方法。通过引入本发明的配体的C10-30烷基链可以通过非共价键涂覆在疏水性纳米颗粒上,从而便于引入各种配体到纳米颗粒中。使用该方法制备的具有各种功能基团的纳米颗粒可以应用于荧光检测、MRI、拉曼光谱、光学检测、PET、SPECT或伽马成像装置,并且可将可视化剂的配体修改以用于新血管检测、癌细胞检测、免疫细胞检测、肝细胞检测、细胞死亡检测和基因检测。
    公开号:
    US20140199235A1
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文献信息

  • Dithiolene Metal Complex Colorless IR Absorbers
    申请人:BASF SE
    公开号:US20160368940A1
    公开(公告)日:2016-12-22
    The invention relates to the use of compounds of formulae (1) and/or (11) as colorless 1R absorbers wherein M is Ni, Pd, Pt, Au, Ir, Fe, Zn, W, Cu, Mo, In, Mn, Co, Mg, V, Cr or Ti, X 1 , X 2 and X 3 are each independently of the others sulfur or oxygen, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are each independently of the others hydrogen, NR 7 R 8 , unsubstituted or substituted C 1 -C 18 alkyl, C 1 -C 18 alkyl wherein the alkylene chain is interrupted with oxygen, unsubstituted or substituted C 1 -C 18 alkenyl, unsubstituted or substituted aryl, unsubstituted or substituted arylalkyl or unsubstituted or substituted heteroarylalkyl, R 7 and R 8 , each independently of the other, being unsubstituted or substituted C 1 -C 18 alkyl, unsubstituted or substituted aryl, un substituted or substituted arylalkyl or unsubstituted or substituted heteroarylalkyl, a further IR absorber optionally being added to the compounds of formulae (I) and (II). The invention relates also to novel dithiolene compounds of formulae (I) and (II) wherein X 1 is oxygen and X 2 and X 3 are oxygen or sulfur. The invention relates furthermore to novel dithiolene compounds of formulae (I) and (II) wherein R 1 to R 6 are NR 7 R 8 .
    该发明涉及将式(1)和/或(11)的化合物用作无色1R吸收剂,其中M为Ni、Pd、Pt、Au、Ir、Fe、Zn、W、Cu、Mo、In、Mn、Co、Mg、V、Cr或Ti,X1、X2和X3分别独立于其他的是或氧,R1、R2、R3、R4、R5和R6分别独立于其他的是氢、NR7R8、未取代或取代的C1-C18烷基、C1-C18烷基,其中烷基链被氧断裂、未取代或取代的C1-C18烯基、未取代或取代的芳基、未取代或取代的芳基烷基或未取代或取代的杂芳基烷基,R7和R8各自独立于另一个是未取代或取代的C1-C18烷基、未取代或取代的芳基、未取代或取代的芳基烷基或未取代或取代的杂芳基烷基,还可以向式(I)和(II)的化合物中添加进一步的红外吸收剂。该发明还涉及式(I)和(II)的新二烯化合物,其中X1为氧,X2和X3为氧或。此外,该发明还涉及式(I)和(II)的新二烯化合物,其中R1至R6为NR7R8。
  • PROTOTYPE SYSTEMS OF THERANOSTIC BIOMARKERS FOR IN VIVO MOLECULAR MANAGEMENT OF CANCER
    申请人:ODYSSEOS Andreani
    公开号:US20160376298A1
    公开(公告)日:2016-12-29
    The present invention relates to a theranostic system comprising a beacon and a compound selected from the group consisting of a quinazoline-based tyrosine kinase inhibitor and a natural product. The theranostic systems have use in the therapy and diagnosis of tyrosine kinase related malignancies.
    本发明涉及一种治疗系统,包括一个信标和从喹唑啉酪氨酸激酶抑制剂天然产物组成的化合物中选择的一种。这种治疗系统在酪氨酸激酶相关恶性肿瘤的治疗和诊断中有用。
  • [EN] ACTIVITY-BASED PROBE COMPOUNDS, COMPOSITIONS, AND METHODS OF USE<br/>[FR] COMPOSÉS SONDES PAR ACTIVITÉ, COMPOSITIONS ET MÉTHODES D'UTILISATION
    申请人:UNIV LELAND STANFORD JUNIOR
    公开号:WO2018119476A1
    公开(公告)日:2018-06-28
    Activity-based probe compounds for use in labeling a cysteine protease are provided. The compounds are targeted to the protease through a specific targeting element. The compounds additionally include a detectable element, such as a fluorescent label, a radiolabel, or a chelator. In some cases, the compounds additionally include a quenching element that is released upon reaction with the protease. Also provided are compositions comprising the compounds and methods for using the compounds, for example in labeling a protease in an animal and in visualizing a tumor in an animal.
    提供用于标记半胱蛋白酶的活性探针化合物。这些化合物通过特定的靶向元素定位到蛋白酶。这些化合物还包括可检测元素,如荧光标记、放射性标记或螯合剂。在某些情况下,这些化合物还包括一种在与蛋白酶反应时释放的熄灭元素。还提供包含这些化合物的组合物和使用这些化合物的方法,例如在动物中标记蛋白酶和在动物中可视化肿瘤。
  • IR DYES FOR FLUORESCENCE IMAGING
    申请人:Ll-COR, INC.
    公开号:US20160144058A1
    公开(公告)日:2016-05-26
    A method for organ imaging, comprising: administering to a subject a diagnostic effective amount of 2-((E)-2-((E)-3-(2-((E)-3,3-dimethyl-5-sulfonato-1-(4-sulfonatobutyl)indolin-2-ylidene)ethylidene)-2-phenoxycyclohex-1-en-1-yl)vinyl)-3,3-dimethyl-1-(4-sulfonatobutyl)-3H-indol-1-ium-5-sulfonate or 2-((E)-2-((E)-3-(2-((E)-3,3-dimethyl-5-sulfonato-1-(4-sulfonatobutyl)indolin-2-ylidene)ethylidene)-2-(4-sulfonatophenoxy)cyclohex-1-en-1-yl)vinyl)-3,3-dimethyl-1-(4-sulfonatobutyl)-3H-indol-1-ium-5-sulfonate. In one embodiment, the organ includes one or more of kidney, bladder, liver, gall bladder, spleen, intestine, heart, lungs and muscle.
    一种用于器官成像的方法,包括:向受试者施用诊断有效量的2-((E)-2-((E)-3-(2-((E)-3,3-二甲基-5-磺酸基-1-(4-磺酸丁基)吲哚啉-2-基亚乙基亚乙烯)-2-苯氧基环己-1-烯-1-基)乙烯)-3,3-二甲基-1-(4-磺酸丁基)-3H-吲哚-1-ium-5-磺酸盐或2-((E)-2-((E)-3-(2-((E)-3,3-二甲基-5-磺酸基-1-(4-磺酸丁基)吲哚啉-2-基亚乙基亚乙烯)-2-(4-磺酸基苯氧基)环己-1-烯-1-基)乙烯)-3,3-二甲基-1-(4-磺酸丁基)-3H-吲哚-1-ium-5-磺酸盐。在一个实施例中,器官包括肾脏、膀胱、肝脏、胆囊、脾脏、肠道、心脏、肺部和肌肉中的一个或多个。
  • MACROPHAGE IDENTIFICATION AGENT, AND IDENTIFICATION METHOD, SORTING METHOD, EVALUATION METHOD, SCREENING METHOD AND KIT USING THE MACROPHAGE IDENTIFIER AGENT
    申请人:CANON KABUSHIKI KAISHA
    公开号:US20160018389A1
    公开(公告)日:2016-01-21
    An object of the present invention is to provide an identification method for a macrophage subtype using an organic compound. Another object of the present invention is to provide a macrophage identification agent containing an organic compound in which a spectral characteristic obtained when the organic compound is added is different depending on a macrophage subtype. Still another object of the present invention is to provide an evaluation method for a macrophage subtype using a macrophage identification agent, an analysis method for correlation between a macrophage subtype and a test substance, a screening method for correlation between a macrophage subtype and a test substance, and a kit. An identification method for a macrophage subtype utilizing that a spectral characteristic obtained with an organic compound added is different depending on a macrophage subtype is provided.
    本发明的一个目的是提供一种利用有机化合物对巨噬细胞亚型进行识别的方法。本发明的另一个目的是提供一种巨噬细胞识别试剂,其中当添加有机化合物时得到的光谱特征取决于巨噬细胞亚型而不同。本发明的另一个目的是提供一种利用巨噬细胞识别试剂进行巨噬细胞亚型评估的方法,一种用于巨噬细胞亚型与测试物之间相关性分析的方法,一种用于巨噬细胞亚型与测试物之间相关性筛选的方法,以及一种试剂盒。提供了一种利用添加有机化合物得到的光谱特征不同取决于巨噬细胞亚型的巨噬细胞亚型识别方法。
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