15401-69-1

  • Product Name:Berberrubine
  • Molecular Formula:C19H16 N O4 . Cl
  • Molecular Weight:357.793
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Product Details

pd_meltingpoint:245℃ (DEC.)

Purity:99%

Manufacturer supply top purity Berberrubine 15401-69-1 with ISO standards

  • Molecular Formula:C19H16 N O4 . Cl
  • Molecular Weight:357.793
  • Vapor Pressure:4.28E-15mmHg at 25°C 
  • Melting Point:245℃ (DEC.) 
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:51.80000 
  • Density:g/cm3 
  • LogP:-0.20270 

berberrubine(Cas 15401-69-1) Usage

InChI:InChI=1/C19H17NO4/c1-22-16-3-2-11-6-15-13-8-18-17(23-10-24-18)7-12(13)4-5-20(15)9-14(11)19(16)21/h2-3,6-9,15,21H,4-5,10H2,1H3

15401-69-1 Relevant articles

Synthesis of Mannich base derivatives of berberine and evaluation of their anticancer and antioxidant effects

Mistry, Bhupendra,Patel, Rahul V.,Keum, Young Soo,Noorzai, Rafi,Gansukh, Enkhtaivan,Kim, Doo Hwan

, p. 73 - 77 (2016)

The 9-demethylated derivative of the iso...

Deciphering the positional impact of chlorine in a new series of berberine analogues towards the superb-selective "turn-on" hydrophobic signaling of bovine serum albumin at physiological pH

Jana, Gopal Chandra,Nayim, Sk,Sahoo, Nandan Kumar,Das, Somnath,Aktara, Mt Nasima,Patra, Anirudha,Islam, Md. Maidul,Hossain, Maidul

, p. 1761 - 1771 (2020)

The optical signals of serum albumin (SA...

Synthesis of berberine-piperazine conjugates as potential antioxidant and cytotoxic agents

Mistry, Bhupendra,Keum, Young Soo,Pandurangan, Muthuraman,Patel, Rahul V.,Kim, Doo Hwan

, p. 2461 - 2470 (2016)

Piperazine derivatives bearing different...

Antibacterial activity and structure-activity relationships of berberine analogs

Iwasa,Kamigauchi,Ueki,Taniguchi

, p. 469 - 478 (1996)

Analogs of berberine 1 and related compo...

Berberine and its metabolites: Relationship between physicochemical properties and plasma levels after administration to human subjects

Spinozzi, Silvia,Colliva, Carolina,Camborata, Cecilia,Roberti, Marinella,Ianni, Cristina,Neri, Flavia,Calvarese, Claudio,Lisotti, Andrea,Mazzella, Giuseppe,Roda, Aldo

, p. 766 - 772 (2014)

Berberine (1) is an alkaloid used widely...

Discovery of novel berberine derivatives with balanced cholinesterase and prolyl oligopeptidase inhibition profile

Sobolova, Katerina,Hrabinova, Martina,Hepnarova, Vendula,Kucera, Tomas,Kobrlova, Tereza,Benkova, Marketa,Janockova, Jana,Dolezal, Rafael,Prchal, Lukas,Benek, Ondrej,Mezeiova, Eva,Jun, Daniel,Soukup, Ondrej,Korabecny, Jan

, (2020)

Berberine, a naturally occurring compoun...

Discovery of 2-aminothiazolyl berberine derivatives as effectively antibacterial agents toward clinically drug-resistant Gram-negative Acinetobacter baumanii

Gao, Wei-Wei,Gopala, Lavanya,Bheemanaboina, Rammohan R. Yadav,Zhang, Guo-Biao,Li, Shuo,Zhou, Cheng-He

, p. 15 - 37 (2018)

Aminothiazolyl berberine derivatives as ...

Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates

Nechepurenko,Shirokova,Khvostov,Frolova,Sinitsyna,Maksimov,Bredikhin,Komarova,Fadeev,Luzina,Tolstikova,Salakhutdinova

, p. 1052 - 1060 (2019)

The paper describes the synthesis of new...

Discovery of natural berberine-derived nitroimidazoles as potentially multi-targeting agents against drug-resistant Escherichia coli

Zhang, Guo-Biao,Maddili, Swetha Kameswari,Tangadanchu, Vijai Kumar Reddy,Gopala, Lavanya,Gao, Wei-Wei,Cai, Gui-Xin,Zhou, Cheng-He

, p. 557 - 568 (2018)

A series of natural berberine-derived ni...

Two telomerase-targeting Pt(ii) complexes of jatrorrhizine and berberine derivatives induce apoptosis in human bladder tumor cells

Qin, Qi-Pin,Wang, Zhen-Feng,Huang, Xiao-Ling,Tan, Ming-Xiong,Luo, Zhi-Hui,Wang, Shu-Long,Zou, Bi-Qun,Liang, Hong

, p. 15247 - 15254 (2019)

Two novel Pt(ii) complexes, [Pt(B-TFA)Cl...

Synthesis, antioxidant and anticancer screenings of berberine-indole conjugates

Mistry, Bhupendra,Keum, Young-Soo,Kim, Doo Hwan

, p. 3241 - 3256 (2016)

A variety of heterocyclic nitrogen cores...

Design, synthesis and biological evaluation of novel Schiff base-bridged tetrahydroprotoberberine triazoles as a new type of potential antimicrobial agents

Duan, Jun-Rong,Liu, Han-Bo,Jeyakkumar, Ponmani,Gopala, Lavanya,Li, Shuo,Geng, Rong-Xia,Zhou, Cheng-He

, p. 907 - 916 (2017)

A series of novel Schiff base-bridged te...

Synthesis and anticancer activity of a novel series of 9-O-substituted berberine derivatives: A lipophilic substitute role

Lo, Chih-Yu,Hsu, Lin-Chen,Chen, Min-Shin,Lin, Yi-Jing,Chen, Lih-Geeng,Kuo, Cheng-Deng,Wu, Jin-Yi

, p. 305 - 309 (2013)

To alter its hydrophobicity, a series of...

Synthesis and anticancer activity of novel 9-O-substituted berberine derivatives

Milata, Viktor,Svedova, Alexandra,Barbierikova, Zuzana,Holubkova, Eva,Cipakova, Ingrid,Cholujova, Dana,Jakubikova, Jana,Panik, Miroslav,Jantova, Sona,Brezova, Vlasta,Cipak, Lubos

, (2019)

Berberine is a bioactive isoquinoline al...

Synthesis, characterization, and biological evaluations of 1,3,5-triazine derivatives of metformin cyclization with berberine and magnolol in the presence of sodium methylate

Cao, Han,Liao, Shili,Zhong, Wenjing,Xiao, Xuerong,Zhu, Jiancheng,Li, Weimin,Wu, Xia,Feng, Yifan

, (2017)

The novel target products were synthesiz...

A novel berberine-based colorimetric and fluorometric probe for Hg2+ detection and its applications in water samples

Gao, Yu,Li, Mingxin,Ruan, Shutang,Wang, Shifa,Wang, Zhonglong,Wu, Suzhen,Yang, Lijuan,Yang, Yiqin,Zhang, Yan

, (2021)

The development of small molecule fluore...

ANTIBACTERIAL ACTIVITY OF BEROLINE

Potapova, E. Yu.,Khaidarov, K. Kh.,Sadykov, Yu. D.

, p. 856 - 857 (1988)

-

Synthetic and antitumor comparison of 9-O-alkylated and carbohydrate-modified berberine derivatives

Wang, Rongchun,Rostyslav, Stoyka,Li, Xiaobin,Lin, Houwen,Zhang, Xuanming,Zhang, Shanshan,Liu, Kechun,Wang, Lizhen

, p. 3251 - 3260 (2020)

Abstract: Berberine is a naturally occur...

Experimental and quantum-chemical study of nucleophilic substitution mechanism in berberine

Burov, Oleg N.,Kletskii, Mikhail E.,Fedik, Nikita S.,Kurbatov, Sergey V.,Lisovin, Anton V.

, p. 997 - 1007 (2015)

Principal differences in the interaction...

Design, synthesis and biological evaluation of a hybrid compound of berberine and magnolol for improvement of glucose and lipid metabolism

Li, Yan,Yuan, Xiao,Rong, Xianglu,Gao, Ying,Qiu, Zhibin,Zhang, Zhipeng,Zhou, Dongbin,Li, Weimin

, p. 81924 - 81931 (2016)

The discovery and structural optimizatio...

Synthesis and evaluation of 9-O-substituted berberine derivatives containing aza-aromatic terminal group as highly selective telomeric G-quadruplex stabilizing ligands

Ma, Yan,Ou, Tian-Miao,Tan, Jia-Heng,Hou, Jin-Qiang,Huang, Shi-Liang,Gu, Lian-Quan,Huang, Zhi-Shu

, p. 3414 - 3417 (2009)

A series of new 9-O-substituted berberin...

Synthesis of piperazine based N-Mannich bases of berberine and their antioxidant and anticancer evaluations

Mistry, Bhupendra,Keum, Young-Soo,Noorzai, Rafi,Gansukh, Enkhtaivan,Kim, Doo Hwan

, p. 531 - 539 (2016)

Isoquinoline alkaloids possess versatile...

Superb-selective chemodosimetric signaling of sulfide in the absence and in the presence of CT-DNA and imaging in living cells by a plant alkaloid berberine analogue

Jana, Gopal Chandra,Khatun, Munira,Nayim, Sk,Das, Somnath,Maji, Anukul,Beg, Maidul,Patra, Anirudha,Bhattacharjee, Paromita,Bhadra, Kakali,Hossain, Maidul

, p. 2368 - 2380 (2019)

The present manuscript reports a lucrati...

Natural Berberine-Hybridized Benzimidazoles as Novel Unique Bactericides against Staphylococcus aureus

Sun, Hang,Ansari, Mohammad Fawad,Fang, Bo,Zhou, Cheng-He

, p. 7831 - 7840 (2021)

Natural berberine-hybridized benzimidazo...

Synthesis, DNA-binding affinities, and binding mode of berberine dimers

Qin, Yong,Pang, Ji-Yan,Chen, Wen-Hua,Cai, Zongwei,Jiang, Zhi-Hong

, p. 25 - 32 (2006)

Six novel berberine dimers (3a-f) were s...

Discovery of novel berberine imidazoles as safe antimicrobial agents by down regulating ROS generation

Wen, Si-Qi,Jeyakkumar, Ponmani,Avula, Srinivasa Rao,Zhang, Ling,Zhou, Cheng-He

, p. 2768 - 2773 (2016)

A series of novel berberine-based imidaz...

synthesis and evolution of berberine derivatives as a new class of antiviral agents against enterovirus 71 through the MEK/ERK pathway and autophagy

Wang, Yan-Xiang,Yang, Lu,Wang, Hui-Qiang,Zhao, Xiao-Qiang,Liu, Ting,Li, Ying-Hong,Zeng, Qing-Xuan,Li, Yu-Huan,Song, Dan-Qing

, (2018)

Taking berberine (BBR) as the lead, 23 n...

Design, synthesis and biological evaluation of berberine-benzimidazole hybrids as new type of potentially DNA-targeting antimicrobial agents

Jeyakkumar, Ponmani,Zhang, Ling,Avula, Srinivasa Rao,Zhou, Cheng-He

, p. 205 - 215 (2016)

A series of novel berberine-benzimidazol...

Synthesis of linked berberine dimers and their remarkably enhanced DNA-binding affinities

Chen, Wen-Hua,Pang, Ji-Yan,Qin, Yong,Peng, Qian,Cai, Zongwei,Jiang, Zhi-Hong

, p. 2689 - 2692 (2005)

This communication describes the facile ...

Design, synthesis and evaluation of a baicalin and berberine hybrid compound as therapeutic agent for ulcerative colitis

Jia, Dan,Dou, Yonghui,Li, Ziwen,Zhou, Xinxin,Gao, Ying,Chen, Keji,Cong, Weihong,Ma, Min,Wu, Zhengzhi,Li, Weimin

, (2020)

Structural modification of active natura...

13-hydroxylation of tetrahydroberberine in cell suspension cultures of some Corydalis species

Iwasa,Kamigauchi

, p. 1511 - 1515 (1996)

Liquid chromatography/atmospheric pressu...

Study of by-products obtained during sanguiritrine production from Macleaya microcapra

Savina,Sheichenko,Tolkachev

, p. 422 - 423 (1997)

-

Anti-Inflammation Associated Protective Mechanism of Berberine and its Derivatives on Attenuating Pentylenetetrazole-Induced Seizures in Zebrafish

Zhang, Baoyue,Wang, Lizhen,Ji, Xiuna,Zhang, Shanshan,Sik, Attila,Liu, Kechun,Jin, Meng

, p. 309 - 325 (2020)

Epileptic seizures are characterized by ...

Synthesis and biological evaluation of berberine derivatives bearing 4-aryl-1-piperazine moieties

Mistry, Bhupendra,Keum, Young-Soo,Kim, Doo Hwan

, p. 470 - 474 (2015)

Piperazine moieties with disubstituted N...

Preparation method of berberrubine hydrochloride

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Paragraph 0021-0042, (2021/03/13)

The invention discloses a preparation me...

Novel berberine derivative as well as synthesis method and application thereof

-

Paragraph 0044-0046, (2021/01/29)

The invention discloses a novel berberin...

Discovery of C-9 modified berberine derivatives as novel lipid-lowering agents

Li, Dong-Dong,Yu, Pan,Xu, Hui,Wang, Zhen-Zhong,Xiao, Wei,Zhao, Lin-Guo

, p. 59 - 66 (2021/01/06)

Berberine (BBR), a kind of quaternary am...

15401-69-1 Process route

berberine chloride
633-65-8

berberine chloride

berberrubine chloride
15401-69-1

berberrubine chloride

Conditions
Conditions Yield
at 180 ℃; for 0.333333h;
98%
In N,N-dimethyl-formamide; at 160 ℃;
94%
at 190 ℃; for 0.333333h;
93.92%
at 190 ℃; for 0.333333h;
93.92%
at 190 ℃; for 3h;
93.9%
In N,N-dimethyl-formamide; for 0.25h; Microwave irradiation;
93%
In N,N-dimethyl-formamide; for 0.25h; Reflux; Microwave irradiation;
92%
berberine chloride; at 180 - 190 ℃;
With hydrogenchloride; In ethanol;
92.4%
at 190 ℃; under 20 - 30 Torr;
90%
at 190 ℃; for 0.25h; under 20 - 30 Torr;
90%
at 190 ℃; for 0.25h; under 20 - 30 Torr;
90%
In 1-methyl-pyrrolidin-2-one; at 150 - 155 ℃; for 3h; Temperature;
90%
at 190 ℃; for 0.75h;
89.8%
at 190 ℃; for 2h; under 20 Torr;
88.2%
at 190 ℃; for 0.25h; under 20 Torr;
88.4%
at 190 ℃; for 2h; under 20 Torr;
88.2%
at 190 ℃; for 0.5h; under 20 Torr;
88.4%
at 190 ℃; under 20 - 30 Torr;
88.7%
at 170 ℃; for 1h; under 750.075 Torr;
88.3%
at 195 ℃; under 30 Torr;
87.5%
With water; at 190 ℃; for 1h; under 0.750075 Torr;
85.9%
at 190 ℃; for 0.666667h; under 20 - 30 Torr;
85%
at 190 ℃; for 0.666667h; under 20 - 30 Torr;
85%
at 190 ℃; for 0.666667h; under 20 - 30 Torr;
85%
at 190 ℃; for 0.666667h; under 20 - 30 Torr;
85%
With hydrogenchloride; In ethanol; at 190 ℃; for 0.25h; under 20 Torr;
84.6%
In neat (no solvent); at 195 - 200 ℃; under 20 - 30 Torr; Temperature;
81%
With hydrogenchloride; In ethanol; at 190 ℃; for 0.333333h;
80%
at 195 - 210 ℃; under 30 - 40 Torr;
80%
berberine chloride; at 195 - 210 ℃;
With hydrogenchloride; In ethanol; water;
80%
for 1h; under 30 - 40 Torr;
80%
at 190 ℃;
79%
With hydrogenchloride; In ethanol; at 190 ℃; for 0.75h; under 20 Torr;
79%
at 190 ℃; Pyrolysis; Inert atmosphere;
79%
at 190 ℃; for 0.5h; under 20 - 30 Torr;
79%
at 205 ℃; for 2h; under 11.2511 Torr;
77%
at 195 - 210 ℃; for 0.5h; under 20 - 30 Torr; Pyrolysis;
74%
at 190 ℃; for 0.25h; under 20 - 30 Torr;
69%
for 0.0833333h; Irradiation;
67%
at 190 ℃; for 0.75h; under 10 - 15 Torr;
65%
In N,N-dimethyl-formamide; at 190 ℃; for 2h;
65%
at 195 ℃; for 0.666667h; regioselective reaction;
62.5%
at 190 ℃;
60%
at 190 ℃; for 0.25h;
60%
at 190 ℃; for 0.5h;
60%
at 195 - 210 ℃; for 0.25h; under 20 - 30 Torr;
60%
at 190 ℃; for 0.5h; Vacuum;
60%
at 190 ℃; for 0.333333h; under 20 - 30 Torr; Inert atmosphere;
60%
at 190 - 210 ℃; for 0.5h; under 30 - 40 Torr;
60%
at 190 ℃; for 0.5h;
60%
With hydrogenchloride; at 190 ℃; for 2h; Inert atmosphere;
50.7%
at 190 ℃; for 0.25h; under 20 - 30 Torr;
660 mg
Heating;
at 190 ℃; for 0.5h;
60 %Spectr.
at 190 ℃; for 0.25h; under 20 - 30 Torr;
berberine chloride; at 195 ℃; for 0.25h;
With hydrogenchloride; In ethanol; at 20 ℃; for 1h;
at 190 ℃; for 1.5h; under 30 Torr;
8.37 g
Multi-step reaction with 2 steps
1: 0.25 h / 190 °C / 30 Torr
2: hydrogenchloride / ethanol / 20 °C
With hydrogenchloride; In ethanol;
at 190 ℃; for 0.666667h; under 20 - 30 Torr;
With piperidine; water; In ethanol; Reagent/catalyst; Solvent; Reflux;
In N,N-dimethyl-formamide; at 190 ℃; Reflux;
at 190 ℃; for 0.5h; under 20 - 30 Torr;
With hydrogenchloride; In ethanol; water; at 190 ℃;
With mercury; at 190 ℃;
at 190 ℃;
at 180 - 200 ℃; for 1.25h; under 20 - 30 Torr;
Multi-step reaction with 2 steps
1: 0.5 h / 185 °C / 20 - 30 Torr
2: hydrogenchloride / ethanol; water / 8 h / 20 °C
With hydrogenchloride; In ethanol; water;
berberine chloride; at 195 - 205 ℃; for 0.5h;
With hydrogenchloride; In ethanol; at 20 ℃; for 1h;
With hydrogenchloride; In ethanol; at 20 - 190 ℃; for 1.33333h;
at 190 ℃;
berberrubine
108275-17-8,6847-93-4

berberrubine

berberrubine chloride
15401-69-1

berberrubine chloride

Conditions
Conditions Yield
With hydrogenchloride; In ethanol; water; at 20 ℃; for 8h;
98%
With hydrogenchloride; In chloroform; Ambient temperature;
94.1%
With hydrogenchloride; In ethanol; water; pH=5 - 6;
82%
With hydrogenchloride; In water;
With hydrogenchloride; In ethanol; at 20 ℃;

15401-69-1 Upstream products

  • 108275-17-8
    108275-17-8

    berberrubine

  • 633-65-8
    633-65-8

    berberine chloride

  • 17388-19-1
    17388-19-1

    berberrubine

  • 68030-18-2
    68030-18-2

    berberine chloride hydrate

15401-69-1 Downstream products

  • 52418-15-2
    52418-15-2

    2,3-methenedioxy-9-cinnamate-10-methoxyprotoberberine chloride

  • 1372875-37-0
    1372875-37-0

    C28H25N2O5(1+)*Cl(1-)

  • 1372875-38-1
    1372875-38-1

    C29H27N2O5(1+)*Cl(1-)

  • 1372875-39-2
    1372875-39-2

    C27H23N2O5(1+)*Cl(1-)

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