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| SKU | Size | Availability |
Price | Qty |
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C421842-1ml
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1ml |
Available within 8-12 weeks(?)
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$69.90
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DNA alkylating agent
| Synonyms | carmustine | 154-93-8 | 1,3-Bis(2-chloroethyl)-1-nitrosourea | BCNU | Carmubris | Carmustin | Gliadel | Nitrumon | BiCNU | Becenun | Bischloroethyl nitrosourea | Bi CNU | Carmustinum | 1,3-Bis(2-chloroethyl)nitrosourea | Bischlorethylnitrosurea | Bischlorethylnitrosourea | Carmustina | Be |
|---|---|
| Specifications & Purity | Moligand™, 10mM in DMSO |
| Biochemical and Physiological Mechanisms | Carmustine is a member of the antineoplastic nitrosourea compounds. Carmustine can perform both alkylating and carabamoylating action and owes part of its cytotoxicity to its demonstrated ability to produce interstrand DNA cross linking. In addition, this |
| Storage Temp | Store at -80°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Grade | Moligand™ |
| Action Type | INHIBITOR |
| Mechanism of action | RNA inhibitor |
| Product Description |
Carmustine is a cell-cycle phase nonspecific alkylating antineoplastic agent General description: Carmustine is a mustard gas related β-chloro-nitrosourea compound, which is used in chemotherapy. It inhibits DNA replication and DNA transcription. Application: Carmustine has been used to select transduced cells expressing MGMTP140K, a foamy virus vector. It has also been used in fluorescence-activated cell sorting (FACS) assay, to test the response of cell lines to carmustine. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Organic carbonic acids and derivatives |
| Subclass | Ureas |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Nitrosoureas |
| Alternative Parents | Semicarbazides Nitrosamides Organopnictogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl chlorides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Nitrosourea - Semicarbazide - Nitrosamide - Organic n-nitroso compound - Organic nitroso compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Alkyl chloride - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Carbonyl group - Alkyl halide - Organic nitrogen compound - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as nitrosoureas. These are compounds containing a nitro group and an urea group N-N linked together, with the general structure R1N(R2)C(=O)N(R3)N=O. |
| External Descriptors | organochlorine compound - N-nitrosoureas |
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| ALogP | 1.5 |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| IUPAC Name | 1,3-bis(2-chloroethyl)-1-nitrosourea |
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| INCHI | InChI=1S/C5H9Cl2N3O2/c6-1-3-8-5(11)10(9-12)4-2-7/h1-4H2,(H,8,11) |
| InChIKey | DLGOEMSEDOSKAD-UHFFFAOYSA-N |
| Smiles | C(CCl)NC(=O)N(CCCl)N=O |
| Isomeric SMILES | C(CCl)NC(=O)N(CCCl)N=O |
| WGK Germany | 3 |
| RTECS | YS2625000 |
| UN Number | 2811 |
| Packing Group | I |
| Molecular Weight | 214.05 |
| Reaxy-Rn | 2049744 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2049744&ln= |
| Sensitivity | Heat sensitive |
|---|---|
| Melt Point(°C) | 32°C(lit.) |
| Molecular Weight | 214.050 g/mol |
| XLogP3 | 1.500 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 4 |
| Exact Mass | 213.007 Da |
| Monoisotopic Mass | 213.007 Da |
| Topological Polar Surface Area | 61.800 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 156.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Yi Xiao, Haomin Yi, Jingzhi Zhu, Suhua Chen, Guofang Wang, Yilong Liao, Yuanyuan Lei, Liyin Chen, Xingcai Zhang, Fangfu Ye. (2023) Evaluation of DNA adduct damage using G-quadruplex-based DNAzyme. Bioactive Materials, 23 (45). |
| 2. Qin Hongkun, Gui Yanping, Ma Rong, Zhang Heng, Guo Yabing, Ye Yuting, Li Jia, Zhao Li, Wang Yajing. (2021) miR-1258 Attenuates Tumorigenesis Through Targeting E2F1 to Inhibit PCNA and MMP2 Transcription in Glioblastoma. Frontiers in Oncology, 11 |
| 3. Hai-Long Yu, Xiao-Long Liang, Zhen-Yang Ge, Zhi Zhang, Yao Ruan, Hao Tang, Qing-Ye Zhang. (2024) Metabolic Flux Analysis of Xanthomonas oryzae Treated with Bismerthiazol Revealed Glutathione Oxidoreductase in Glutathione Metabolism Serves as an Effective Target. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 25 (22): (12236). |