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ungeremine

Product Name
ungeremine
CAS No.
2121-12-2
Chemical Name
ungeremine
Synonyms
C12189;ungeremine;Ungerimine;Lycobetaine(Ungeremine);[1,3]Dioxolo[4,5-j]pyrrolo[3,2,1-de]phenanthridinium, 4,5-dihydro-2-hydroxy-
CBNumber
CB61329876
Molecular Formula
C16H12NO3
Formula Weight
266.275
MOL File
2121-12-2.mol
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ungeremine Property

Melting point:
270-272℃ (dec.)
Boiling point:
409.48°C (rough estimate)
Density 
1.1727 (rough estimate)
refractive index 
1.5300 (estimate)
storage temp. 
-20°C
solubility 
Methanol: 10 mg/ml
form 
A solid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
INB0003897
Product name
UNGEREMINE
Purity
95.00%
Packaging
5MG
Price
$500.34
Updated
2021/12/16
Biorbyt Ltd
Product number
orb573053
Product name
Lycobetaine (Ungeremine)
Purity
>98%,Standard References Grade
Packaging
100mg
Price
$765
Updated
2021/12/16
Biorbyt Ltd
Product number
orb573053
Product name
Lycobetaine (Ungeremine)
Purity
>98%,Standard References Grade
Packaging
250mg
Price
$1208.7
Updated
2021/12/16
Biorbyt Ltd
Product number
orb573053
Product name
Lycobetaine (Ungeremine)
Purity
>98%,Standard References Grade
Packaging
1g
Price
$2395.3
Updated
2021/12/16
DC Chemicals
Product number
DC23020
Product name
Lycobetaine(Ungeremine)
Purity
>98%,StandardReferencesGrade
Packaging
100mg
Price
$500
Updated
2021/12/16
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ungeremine Chemical Properties,Usage,Production

Description

Ungeremine is a betaine-type alkaloid that has been found in C. zeylanicum and has diverse biological activities.1,2,3,4 It is an inhibitor of acetylcholinesterase (AChE; IC50 = 0.35 µM).2 Ungeremine acts as a topoisomerase poison, inducing double-strand breaks in DNA by stabilizing the linkage between topoisomerase IIβ and DNA.3 It inhibits the relaxation of supercoiled DNA by human topoisomerase I and -IIα and E. coli topoisomerase I and -IV (IC50s = 6.1, 25.8, 15, and 7.3 µM, respectively).4 Ungeremine inhibits the growth of HL-60, MOLT-4, K562, U937, and LXFL 529L cells (IC50s = 1.3, 0.7, 0.8, 2.5, and 1.2 µM, respectively). It is cytotoxic to a variety of drug-sensitive and -resistant cancer cells (IC50s = 4.89-6.45 and 3.67-75.24 µM, respectively) and induces ferroptosis, necroptosis, apoptosis, and autophagy in CCRF-CEM leukemia cells. Ungeremine (60 mg/kg twice per week) also reduces tumor growth in a GXF251L mouse xenograft model.3WARNING This product is not for human or veterinary use.

Definition

ChEBI: A natural product found particularly in Pancratium maritimum and Nerine bowdenii.

ungeremine Preparation Products And Raw materials

Raw materials

Preparation Products

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ungeremine Suppliers

Sichuan Wei Keqi Biological Technology Co., Ltd.
Tel
028-81700200 18116577057
Fax
028-81705658
Email
3003855609@qq.com
Country
China
ProdList
7778
Advantage
56
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9803
Advantage
58
Chengdu Push Bio-Technology Co., Ltd.
Tel
028-028-85370565-229-229 18080489829
Email
18080489829@163.com
Country
China
ProdList
8250
Advantage
60
Shanghai Standard Technology Co.,Ltd.
Tel
021-021-57127007-6622-6622 17621252073
Fax
+86 (21) 5132-0077
Email
luzh@nature-standard.com
Country
China
ProdList
3021
Advantage
58
Qingdao haohai anjie pharmaceutical technology co., ltd.
Tel
156-6622-8711 18639325623
Email
chen.wanglin@hmgj.group
Country
China
ProdList
1905
Advantage
58
Naturewill Biotechnology Co., Ltd.
Tel
028-82632533 18113192475
Email
3157321941@qq.com
Country
China
ProdList
4993
Advantage
58
Cayman Chemical Company
Tel
800-364-9897
Email
sales@caymanchem.com
Country
China
ProdList
6838
Advantage
58

2121-12-2, ungeremineRelated Search:


  • C12189
  • ungeremine
  • [1,3]Dioxolo[4,5-j]pyrrolo[3,2,1-de]phenanthridinium, 4,5-dihydro-2-hydroxy-
  • Ungerimine
  • Lycobetaine(Ungeremine)
  • 2121-12-2
  • C16H12NO3