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Lactoyl-CoA
Venetoclax
Cryptolepine
10001-82-8
Cefepime Impurity A
chem960
480-26-2
480-26-2
(name: Cryptolepine)
Product Name:
Cryptolepine
CAS No:
480-26-2
MF:
C16H12N2
MW:
232.279883384705
CID:
931671
PubChem ID:
82143
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Related Compounds
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SN-38 | 86639-52-3
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Basic Information
World Suppliers
Introduction
白叶藤碱是西非国家药用植物白叶藤中主要的生物碱,白叶藤碱具有丰富的生物活性。在生物作用机理研究中发现,白叶藤碱能够插入到DNA碱基对之间,是一个典型的DNA插入剂,具有稳定DNA-拓扑异构酶Ⅱ共价复合物的作用,是潜在的拓扑异构酶Ⅱ抑制剂
Names and Identifiers
cryptolepine
Cryptolepine hydrate
5H-Quindoline, 5-methyl-
5-METHYL-5H-INDOLO[3,2-B]QUINOLINE
AC1Q4UOU
C09142
CCRIS 9019
NSC647765
SureCN542771
5-methylindolo[3,2-b]quinoline
OF1UIT4RDH
5-Methylquindoline
5-Methyl-5H-quindoline hydrate
BDBM50412201
Q5190964
5-Methyl-5H-quindoline
DR1
Cryptolepine
UNII-OF1UIT4RDH
MFCD17215953
480-26-2
CHEMBL119096
CHEBI:3930
KURWKDDWCJELSV-UHFFFAOYSA-N
BDBM50589259
A936359
SCHEMBL542771
DTXSID6037645
CIV5_1.1
ConMedNP.69
展開
InChIKey:KURWKDDWCJELSV-UHFFFAOYSA-N
Inchi:1S/C16H12N2/c1-18-15-9-5-2-6-11(15)10-14-16(18)12-7-3-4-8-13(12)17-14/h2-10H,1H3
SMILES:N1(C)C2C=CC=CC=2C=C2C1=C1C=CC=CC1=N2
Chemical and Physical Properties
Computed Properties
精确分子量: 232.10016
氢键供体数量: 0
氢键受体数量: 1
可旋转化学键数量: 0
同位素质量: 232.100048391g/mol
重原子数量: 18
复杂度: 316
同位素原子数量: 0
确定原子立构中心数量: 0
不确定原子立构中心数量: 0
确定化学键立构中心数量: 0
不确定化学键立构中心数量: 0
共价键单元数量: 1
疏水参数计算参考值(XlogP): 3.3
互变异构体数量: none
表面电荷: 0
拓扑分子极性表面积: 17.8
Experimental Properties
PSA: 15.6
溶解度: DMSO: ≥5mg/mL
Security Information
安全说明:26-39
危險品標誌: Xn
危险类别码:22-37/38-41
储存的条件:贮存在阴凉处。 容器保持紧闭,储存在干燥通风处。 建议的贮存温度: 2 - 8 °C
危险性概述:急性毒性, 经口 (类别4) 皮肤刺激 (类别2) 严重的眼损伤 (类别1) 特异性靶器官系统毒性(一次接触) (类别3)
Related Literature
1.
Cryptolepine and quindoline: understanding their photophysics
Inês F. A. Mariz,Sandra Pinto,Jo?o Lavrado,Alexandra Paulo,José M. G. Martinho,Ermelinda M. S. Ma??as
Phys. Chem. Chem. Phys. 2017 19 10255
2.
Recent synthetic efforts in the preparation of 2-(3,4)-alkenyl (aryl) quinoline molecules towards anti-kinetoplastid agents
Dayana Orozco,Vladimir V. Kouznetsov,Armando Bermúdez,Leonor Y. Vargas Méndez,Arturo René Mendoza Salgado,Carlos Mario Meléndez Gómez
RSC Adv. 2020 10 4876
3.
Synthesis, analysis and biological evaluation of novel indolquinonecryptolepine analogues as potential anti-tumour agents
A. Le Gresley,V. Gudivaka,S. Carrington,A. Sinclair,J. E. Brown
Org. Biomol. Chem. 2016 14 3069
4.
Fluorescent natural products as probes and tracers in biology
Romain Duval,Christophe Duplais
Nat. Prod. Rep. 2017 34 161
5.
The uniqueness and therapeutic value of natural products from West African medicinal plants. Part I: uniqueness and chemotaxonomy
Fidele Ntie-Kang,Lydia L. Lifongo,Conrad V. Simoben,Smith B. Babiaka,Wolfgang Sippl,Luc Meva'a Mbaze
RSC Adv. 2014 4 28728
6.
Imaging and therapeutic applications of Zn(ii)-cryptolepine–curcumin molecular probes in cell apoptosis detection and photodynamic therapy
Qi-Pin Qin,Zu-Zhuang Wei,Zhen-Feng Wang,Xiao-Ling Huang,Ming-Xiong Tan,Hua-Hong Zou,Hong Liang
Chem. Commun. 2020 56 3999
7.
Recent developments in research on terrestrial plants used for the treatment of malaria
Colin W. Wright
Nat. Prod. Rep. 2010 27 961
8.
Synthesis of 3-aminoquinolines from α-imino rhodium carbenes and 2-aminobenzaldehydes
Jiani Li,Jing Feng,Tao Chen,Ze-Feng Xu,Chuan-Ying Li
Org. Biomol. Chem. 2023 21 5935
9.
Synthesis of 3-aminoquinolines from α-imino rhodium carbenes and 2-aminobenzaldehydes
Jiani Li,Jing Feng,Tao Chen,Ze-Feng Xu,Chuan-Ying Li
Org. Biomol. Chem. 2023 21 5935
10.
Microwave-assisted reductive cyclization: an easy entry to the indoloquinolines and spiro[2H-indole-2,3′-oxindole]
Prakash T. Parvatkar,Mahesh S. Majik
RSC Adv. 2014 4 22481
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