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Nitidine chloride

CAS No.
13063-04-2
Chemical Name:
Nitidine chloride
Synonyms
NITIDINE;Angolinine;Nitidine chloride;NITIDINE CHLORIDE (RG);ShinyleafPricklyashRoot;dimethoxy-12-methyl-,chloride;Nitidine, chloride (6CI, 7CI, 8CI);[1,3]Dioxolo[4,5]benzo[1,2-c]phenanthridinium, 2,3-;Nitidine chloride, 98%, from Zanthoxylum nitidum (Roxb.) DC.;2,3-Dimethoxy-12-methyl-(1,3)-benzodioxolo(5,6-c)phenanthridinium chloride
CBNumber:
CB4341347
Molecular Formula:
C21H18NO4+
Molecular Weight:
348.37
MDL Number:
MFCD01659688
MOL File:
13063-04-2.mol
Last updated:2023-08-24 17:20:48

Nitidine chloride Properties

Melting point 283-286 °C
storage temp. -20°C
solubility DMSO: soluble1mg/mL, clear (warmed)
form powder
color white to beige
InChIKey QLDAACVSUMUMOR-UHFFFAOYSA-M
FDA UNII XO8WQL69T8

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Danger
Hazard statements  H300
Precautionary statements  P264-P270-P301+P310-P321-P330-P405-P501
Safety Statements  24/25
WGK Germany  3
RTECS  DF4935500
HS Code  29399990
Toxicity mouse,LD50,intraperitoneal,98980ug/kg (98.98mg/kg),National Cancer Institute Screening Program Data Summary, Developmental Therapeutics Program. Vol. JAN1986,
NFPA 704
0
4 0

Nitidine chloride price More Price(35)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 29223 Nitidine (chloride) 13063-04-2 10mg $107 2024-03-01 Buy
Cayman Chemical 29223 Nitidine (chloride) 13063-04-2 100mg $929 2024-03-01 Buy
Cayman Chemical 29223 Nitidine (chloride) 13063-04-2 5mg $57 2024-03-01 Buy
Cayman Chemical 29223 Nitidine (chloride) 13063-04-2 25mg $249 2024-03-01 Buy
TRC N490110 Nitidine chloride 13063-04-2 25mg $295 2021-12-16 Buy
Product number Packaging Price Buy
29223 10mg $107 Buy
29223 100mg $929 Buy
29223 5mg $57 Buy
29223 25mg $249 Buy
N490110 25mg $295 Buy

Nitidine chloride Chemical Properties,Uses,Production

Description

This quaternary alkaloid occurs primarily in Zanthoxylum nitidum (Lam.) DC but has also been found in several species of Fagara. It is normally isolated as the chloride which forms bright yellow needles when recrystallized from EtOH-HCl. The crystals decompose on heating to 240°C yielding a product having m.p. 285-6°C. The iodide also forms yellow needles and undergoes a similar trans_x0002_formation at the same temperature to yield a product with the same melting point, possibly identical to that obtained from the chloride. The crystalline acetate, m.p. 255-260°C and the pseudocyanide, m.p. 215-6°C and decomposing completely at 234°C in vacuo have also been prepared. A periodide, which fonns chocolate-brown needles when crystallized from Me2CO, m.p. 300-1 °c (dec.) is useful for characterizing the base.

Uses

Nitidine Chloride shows the ability to inhibit hepatic cancer growth through modulation of signaling pathways.

Preparation

A solution of 1555 (0.102 g, 0.278 mmol) and triphosgene (0.179 g, 0.602 mmol) in acetonitrile (2.5 mL) was stirred at 60 C° (bath temperature) for 0.5 h. After the addition of ice/water, a yellow precipitate was collected by filtration and recrystallized from ethanol/diethyl ether to directly afford nitidine chloride (0.098 g, 91%); mp 285–292 C°.
13063-04-2 synthesis
An isocyano group can serve as both a protecting group for the amino function, and, due to its electronic effect, as an activating group as well. These two functionalities are employed in a synthetic route whereby an amino function has to be protected and a condensation reaction is performed at the a-carbon atom, for which activation is required.
3,4-Fused tryptophan analogues 1563 and 1564 contain a ring that bridges the a-carbon and the 4-position of the indole ring, thus limiting the conformational flexibility of the side chain. The synthesis proceeds from N-formylated 40-bromotryptophan 1558 via isocyanide 1559, 2-propenoate 1560, and Pd-catalyzed cyclization of the a-2-propenyl dl-tryptophan derivatives 1561 and 1562 to give both the seven- and eight-membered constrained ring analogues 1564 and 1563. Dehydration of the formamide 1558 with triphosgene affords the isocyanide 1559 in 75% (87%) yield.

Biochem/physiol Actions

Nitidine chloride is a natural product with anti-cancer activity. Its mechanism of action likely involves several pathways. Nitidine chloride has been found to inhibit topoisomerase I and topoisomerase II, induce cell apoptosis by activation of the caspase-dependent pathway, suppress c-Src/FAK associated signaling pathways and suppress Janus kinase 2/STAT3 signaling and the expression of STAT3-dependent target genes, including cyclin D1, Bcl-xL, and VEGF. Nitidine chloride has also been found to have anti-malaria activity.

References

Arthur, Hui, Ng., Chern. Ind., 1514 (1958)
Arthur, Hui, Ng.,J. Chern. Soc., 1840 (1959)
Kuck, Albonico, Deulofeu., Chern. Ind., 945 (1966)

548-31-2
13063-04-2
Synthesis of Nitidine chloride from (1,3)Benzodioxolo(5,6-c)phenanthridin-13(12H)-one, 2,3-dimethoxy-12-methyl-
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View Lastest Price from Nitidine chloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Nitidine chloride pictures 2024-04-12 Nitidine chloride
13063-04-2
US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
Nitidine Chloride  pictures 2023-02-24 Nitidine Chloride
13063-04-2
US $0.00 / mg 5mg ≥97%(HPLC) 10 g Shanghai Standard Technology Co., Ltd.
Nitidine chloride pictures 2019-07-06 Nitidine chloride
13063-04-2
US $1.00 / kg 1g 99% 100KG Career Henan Chemical Co
  • Nitidine Chloride  pictures
  • Nitidine Chloride
    13063-04-2
  • US $0.00 / mg
  • ≥97%(HPLC)
  • Shanghai Standard Technology Co., Ltd.

Nitidine chloride Spectrum

2,3-Dimethoxy-12-methyl-(1,3)-benzodioxolo(5,6-c)phenanthridinium chloride Nitidine chloride [1,3]Dioxolo[4,5]benzo[1,2-c]phenanthridinium, 2,3- dimethoxy-12-methyl-,chloride NITIDINE 2,3-DiMethoxy-12-Methyl-[1,3]dioxolo[4',5':4,5]benzo[1,2-c]phenanthridin-12-iuM chloride Angolinine NITIDINE CHLORIDE (RG) Nitidine chloride, 98%, from Zanthoxylum nitidum (Roxb.) DC. ShinyleafPricklyashRoot Nitidine, chloride (6CI, 7CI, 8CI) 1,3]Benzodioxolo[5,6-c]phenanthridinium, 2,3-dimethoxy-12-methyl-, chloride (1:1) 2,3-Dimethoxy-12-methyl-[1,3]dioxolo[4',5':4,5]benzo[1,2-c]phenanthridin-12-ium chloride 13063-04-2 13113063-02-2 C21H17NO4HCl Active Pharmaceutical Ingredients chemical reagent pharmaceutical intermediate phytochemical reference standards from Chinese medicinal herbs (TCM). standardized herbal extract