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| SKU | Size | Availability |
Price | Qty |
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A114343-1g
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1g |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
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$171.90
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Microtubule depolymerizing agent; affects tubulin dynamics
| Synonyms | DTXCID202563 | HMS1568B16 | HMS1922K04 | Zenteltrade mark | Albendazole (USAN:USP:INN:BAN:JAN) | HSDB 7444 | methoxy-N-(5-propylthiobenzimidazol-2-yl)carboxamide | ALBENDAZOLE (EP MONOGRAPH) | ALBENDAZOLE (MART.) | Albendazole [USAN:USP:INN:BAN:JAN] | Opr |
|---|---|
| Specifications & Purity | analytical standard, ≥99% |
| Biochemical and Physiological Mechanisms | Anthelmintic benzimidazole and microtubule depolymerizing agent. Able to inhibit brain microtubule polymerization in vitro and delays microtubule assembly in vivo . Anti-tumour activity seen in vivo . |
| Shipped In | Normal |
| Grade | analytical standard |
| Action Type | INHIBITOR |
| Mechanism of action | Tubulin inhibitor |
| Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Benzimidazoles |
| Subclass | 2-benzimidazolylcarbamic acid esters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | 2-benzimidazolylcarbamic acid esters |
| Alternative Parents | Thiophenol ethers Alkylarylthioethers Imidazoles Heteroaromatic compounds Carbamate esters Organic carbonic acids and derivatives Sulfenyl compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | 2-benzimidazolylcarbamic acid ester - Aryl thioether - Thiophenol ether - Alkylarylthioether - Benzenoid - Azole - Imidazole - Carbamic acid ester - Heteroaromatic compound - Carbonic acid derivative - Thioether - Azacycle - Sulfenyl compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as 2-benzimidazolylcarbamic acid esters. These are aromatic heteropolycyclic compounds that contain a carbamic acid ester group, which is N-linked to the C2-atom of a benzimidazole moiety. |
| External Descriptors | a small molecule |
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| ALogP | 2.9 |
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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 | methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate |
|---|---|
| INCHI | InChI=1S/C12H15N3O2S/c1-3-6-18-8-4-5-9-10(7-8)14-11(13-9)15-12(16)17-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16) |
| InChIKey | HXHWSAZORRCQMX-UHFFFAOYSA-N |
| Smiles | CCCSC1=CC2=C(C=C1)N=C(N2)NC(=O)OC |
| Isomeric SMILES | CCCSC1=CC2=C(C=C1)N=C(N2)NC(=O)OC |
| WGK Germany | 2 |
| RTECS | FD1100000 |
| Molecular Weight | 265.33 |
| Reaxy-Rn | 4193299 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4193299&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jul 17, 2023 | A114343 |
| Solubility | Slightly soluble in acetone or chloroform, insoluble in water, slightly soluble in hot dilute hydrochloric acid, soluble in methanol, ethanol, acetic acid, etc. |
|---|---|
| Melt Point(°C) | 208-210°C |
| Molecular Weight | 265.330 g/mol |
| XLogP3 | 2.900 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Exact Mass | 265.088 Da |
| Monoisotopic Mass | 265.088 Da |
| Topological Polar Surface Area | 92.300 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 290.000 |
| 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. Zhiwei Zhou, Yaohua Yan, Xing Li, Fanxi Zeng, Senlin Shao. (2023) Effect of urea-based chemical cleaning on TrOCs rejection by nanofiltration membranes. SEPARATION AND PURIFICATION TECHNOLOGY, 315 (123662). |
| 2. Yiting Wen, Yujia Zhang, Xiaoli Zhang, Linjun Wang, Qiuxia Pan, Qiuhan Bai, Du Zhu, Weiming Chai. (2023) Inhibition of albendazole and 2-(2-aminophenyl)-1H-benzimidazole against tyrosinase: mechanism, structure–activity relationship, and anti-browning effect. JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 103 (6): (2824-2837). |
| 3. Tianfeng Yang, Cheng Cheng, Rui Xu, Jian Huo, Xiujuan Peng, Yanbin Chen, Yonghong Liang, Zhiheng Su, Yanmin Zhang. (2022) Albendazole exerts an anti-hepatocellular carcinoma effect through a WWOX-dependent pathway. LIFE SCIENCES, 310 (121086). |
| 4. Yaowei Guo, Jin Liu, Qinglin Tang, Cuicui Li, Yanying Zhang, Yao Wang, Yanxin Wang, Yupeng Bi, Christopher D. Snow, Matt J. Kipper, Laurence A. Belfiore, Jianguo Tang. (2022) Lanthanide (Eu3+/Tb3+)-Loaded γ-Cyclodextrin Nano-Aggregates for Smart Sensing of the Anticancer Drug Irinotecan. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 23 (12): (6597). |
| 5. Lei Men, Yuhan Zhang, Keke Li, Zhongyu Li, Chunbin Li, Xueyuan Zhang, Xiaojie Gong, Linlin Fang. (2022) Metabolism and pharmacokinetics of mebendazole in Japanese pufferfish (Takifugu rubripes). Food Additives and Contaminants Part A-Chemistry Analysis Control Exposure & Risk Assessment, |
| 6. Jingfeng Li, Zhaoyi An, Junyang Sun, Chunyan Tan, Dan Gao, Ying Tan, Yuyang Jiang. (2020) Highly Selective Oxidation of Organic Sulfides by a Conjugated Polymer as the Photosensitizer for Singlet Oxygen Generation. ACS Applied Materials & Interfaces, 12 (31): (35475–35481). |
| 7. Dongze Wang, Gang Chen, Xuemei Li, Qiong Jia. (2019) Hypercrosslinked β-cyclodextrin porous polymer as adsorbent for effective uptake towards albendazole from aqueous media. SEPARATION AND PURIFICATION TECHNOLOGY, 227 (115720). |
| 8. Dongze Wang, Xuemei Li, Xiangqun Jin, Qiong Jia. (2019) Design of cucurbit[6]uril-based hypercrosslinked polymers for efficient capture of albendazole. SEPARATION AND PURIFICATION TECHNOLOGY, 216 (9). |
| 9. Qin Li, Xuanping Tan, Lingli Fu, Qu Liu, Weiwei Tang. (2015) A novel fluorescence and resonance Rayleigh scattering probe based on quantum dots for the detection of albendazole. Analytical Methods, 7 (2): (614-620). |
| 10. Lan Sumin, Chen Kexi, Feng Liqiang, Sima Panle, Ji Xiaoyao, Wu Feihua, Lin Yining. (2025) Tea Saponins: a Novel Stabilizer for Enhancing the Oral Bioavailability of Albendazole Nanocrystals. AAPS PHARMSCITECH, 26 (1): (1-13). |