Determine the necessary mass, volume, or concentration for preparing a solution.
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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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N302245-1g
|
1g |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
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$469.90
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N302245-5g
|
5g |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$1,113.90
|
|
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N302245-25g
|
25g |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$3,091.90
|
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N302245-100g
|
100g |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$8,035.90
|
|
| Synonyms | PHENFORMIN | 114-86-3 | N-Phenethylbiguanide | Fenformin | Phenformine | Phenethyldiguanide | Fenformina | Pedg | Phenylethylbiguanide | Cronoformin | Fenfoduron | Fenormin | Glukopostin | Phenformix | Debeone | Diabis | Dibiraf | Dibotin | Glyphen | Retardo | Db-retard | Imidodicarbonimidic diam |
|---|---|
| Specifications & Purity | ≥98% |
| Storage Temp | Store at 2-8°C |
| Shipped In |
Wet ice This product requires cold chain shipping. Ground and other economy services are not available. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Class | Organonitrogen compounds |
| Subclass | Guanidines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Biguanides |
| Alternative Parents | Benzene and substituted derivatives Carboximidamides Organopnictogen compounds Imines Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Biguanide - Benzenoid - Monocyclic benzene moiety - Carboximidamide - Organopnictogen compound - Hydrocarbon derivative - Imine - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as biguanides. These are organic compounds containing two N-linked guanidines. |
| External Descriptors | biguanides |
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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-(diaminomethylidene)-2-(2-phenylethyl)guanidine |
|---|---|
| INCHI | InChI=1S/C10H15N5/c11-9(12)15-10(13)14-7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H6,11,12,13,14,15) |
| InChIKey | ICFJFFQQTFMIBG-UHFFFAOYSA-N |
| Smiles | C1=CC=C(C=C1)CCN=C(N)N=C(N)N |
| Isomeric SMILES | C1=CC=C(C=C1)CCN=C(N)N=C(N)N |
| Molecular Weight | 205.26 |
| Reaxy-Rn | 22781826 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=22781826&ln= |
| Refractive Index | 1.6380 (estimate) |
|---|---|
| Boil Point(°C) | 333.94°c (rough estimate) |
| Melt Point(°C) | 176.5 °C |
| Molecular Weight | 205.260 g/mol |
| XLogP3 | -0.800 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 4 |
| Exact Mass | 205.133 Da |
| Monoisotopic Mass | 205.133 Da |
| Topological Polar Surface Area | 103.000 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 236.000 |
| 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. Zixian He, Zhiwei Liu, Haihuan Xie, Pengjie Luo, Xiangmei Li. (2023) An Ultrasensitive Lateral Flow Immunoassay Based on Metal-Organic Framework-Decorated Polydopamine for Multiple Sulfonylureas Adulteration in Functional Foods. Foods, 12 (3): (539). |
| 2. Haihuan Xie, Yingying Li, Jin Wang, Yi Lei, Anastasios Koidis, Xiangmei Li, Xing Shen, Zhenlin Xu, Hongtao Lei. (2022) Broad-specific immunochromatography for simultaneous detection of various sulfonylureas in adulterated multi-herbal tea. FOOD CHEMISTRY, 370 (131055). |
| 3. Lingli Huang, Di Xiao, Tianyu Wu, Xin Hu, Jun Deng, Xinjian Yan, Jingtao Wu, Simeng Xu, Xiaoping Yang, Gaofeng Li. (2021) Phenformin synergistically sensitizes liver cancer cells to sorafenib by downregulating CRAF/ERK and PI3K/AKT/mTOR pathways. American Journal of Translational Research, 13 (7): ( 7508–7523). |
| 4. Tianyu Wu, Sichun Zhou, Mei Qin, Jing Tang, Xinjian Yan, Lingli Huang, Meiyuan Huang, Jun Deng, Di Xiao, Xin Hu, Jingtao Wu, Xiaoping Yang, Gaofeng Li. (2021) Phenformin and ataxia-telangiectasia mutated inhibitors synergistically co-suppress liver cancer cell growth by damaging mitochondria. FEBS Open Bio, 11 (5): (1440-1451). |
| 5. Peng Mei, Deng Jun, Zhou Sichun, Xiao Di, Long Jiahui, Zhang Nan, He Caimei, Mo Miao, Yang Xiaoping. (2019) Dual Inhibition of Pirarubicin-Induced AKT and ERK Activations by Phenformin Sensitively Suppresses Bladder Cancer Growth. Frontiers in Pharmacology, 10 (1159). |
| 6. Huang Yanjun, Zhou Sichun, He Caimei, Deng Jun, Tao Ting, Su Qiongli, Darko Kwame Oteng, Peng Mei, Yang Xiaoping. (2018) Phenformin alone or combined with gefitinib inhibits bladder cancer via AMPK and EGFR pathways. Cancer Communications, 38 (1): (1-14). |