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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
Molecular Weight:
266.275
MDL Number:
MFCD01716209
MOL File:
2121-12-2.mol
MSDS File:
SDS
Last updated:2025-08-21 11:10:07

ungeremine Properties

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
FDA UNII 9EVC5B2RPS

ungeremine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 34549 Ungeremine ≥98% 2121-12-2 1mg $54 2026-04-30 Buy
Cayman Chemical 34549 Ungeremine ≥98% 2121-12-2 5mg $238 2026-04-30 Buy
Cayman Chemical 34549 Ungeremine ≥98% 2121-12-2 10mg $418 2026-04-30 Buy
Cayman Chemical 34549 Ungeremine ≥98% 2121-12-2 25mg $913 2026-04-30 Buy
Biorbyt Ltd orb573053 Lycobetaine (Ungeremine) >98%,StandardReferencesGrade 2121-12-2 100mg $640 2026-05-06 Buy
Product number Packaging Price Buy
34549 1mg $54 Buy
34549 5mg $238 Buy
34549 10mg $418 Buy
34549 25mg $913 Buy
orb573053 100mg $640 Buy

ungeremine Chemical Properties,Uses,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

ungeremine Suppliers

Global( 14)Suppliers
Supplier Tel Email Country ProdList Advantage
Sichuan Wei Keqi Biological Technology Co., Ltd. 028-81700200 18116577057 3003855609@qq.com China 7717 56
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9799 58
Chengdu Push Bio-Technology Co., Ltd. 028-85370565-229 18080489829 18080489829@163.com China 8379 60
Shanghai Standard Technology Co.,Ltd. 021-021-57127007-6622-6622 17621252073 luzh@nature-standard.com China 3021 58
BOC Sciences +1-631-485-4226 inquiry@bocsci.com United States 19935 58
Qingdao haohai anjie pharmaceutical technology co., ltd. 156-6622-8711 18639325623 chen.wanglin@hmgj.group China 1900 58
Naturewill Biotechnology Co., Ltd. 028-82632533 18113192475 3157321941@qq.com China 4993 58
Chengdu Biopurify Ltd. 82633860 18982077548 cwb1@biopurify.cn China 4630 58
Chengdu Biopurify Phytochemicals Ltd. +86-28-82633860; +86-18080483897 sales@biopurify.com China 4616 58
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