Cas no 179324-69-7 (Bortezomib)
Bortezomib Chemical and Physical Properties
Names and Identifiers
-
- Bortezomib
- MG-341
- PS-341
- [(1r)-3-methyl-1-[[(2s)-1-oxo-3-phenyl-2-[(pyrazinylcarbonyl)amino]propyl]amino]butyl]-boronic acid
- dpba
- VELCADE
- VELCADE(BORTEZOMIB)
- Boronic acid, B-[(1R)-3-methyl-1-[[(2S)-1-oxo-3-phenyl-2-[(2-pyrazinylcarbonyl)amino]propyl]amino]butyl]-
- Bortezomib for research
- Bortezomib (PS-341)
- ((R)-3-Methyl-1-((S)-3-phenyl-2-(pyrazine-2-carboxamido)propanamido)butyl)boronic acid
- bortezomib(Velcade?, Bortecad?, PS-341,MG-341)
- Bortizomib
-  
- Bortezmib
- Bortezomib Base
- MG-341 PS-341
- PS341
- Radiciol
- MLM341
- BortezoMib R
- BortezoMib-D8
- MG-341 PS-341
- Ps 341
- N-[(1R)-1-(DIHYDROXYBORYL)-3-METHYLBUTYL]-N-(PYRAZIN-2-YLCARBONYL)-L-PHENYLALANINAMIDE
- Bortezomib (Velcade)
- [(1R)-3-methyl-1-[[(2S)-3-phenyl-2-(pyrazine-2-carbonylamino)propanoyl]amino]butyl]boronic acid
- [(1R)-3-Methyl-1-[[(2S)-1-oxo-3-phenyl-2-[(pyrazinylcarbonyl)amino]propyl]amino]butyl]boronic acid
- Peptide boronate
- 69G8BD63PP
- Boronic acid, B-[(1R)-3-methyl-1-[[(2S)-1-oxo-3-phenyl
- LDP-341
- PS 341 (pharmaceutical)
- Radiciol , NSC 681239 , MG 341 , DPBA , Brotezamide , LDP 341
- CHEBI:52717
- S1013
- (1R)-3-Methyl-1-({(2S)-3-phenyl-2-[(2-pyrazinylcarbonyl)amino]propanoyl}amino)butylboronic acid, AldrichCPR
- HB4036
- NCGC00242506-07
- Bortezomib accord
- NSC-756655
- EN300-657180
- Bortezomib [USAN:INN:BAN]
- MLS004774142
- L01XX32
- HY-10227
- D03150
- BORTEZOMIB (MART.)
- NSC-681239
- Velcade (Millenium)
- AB01273951-01
- NSC756655
- BORTEZOMIB [JAN]
- SR-01000939863-2
- Boronic acid, [(1(R)-3-methyl-1-[[(2S)-1-oxo-3-phenyl-2-[(pyrazinylcarbonyl)amino]propyl]amino]butyl]-
- SW208077-3
- [(1R)-3-Methyl-1-[[(2S)-1-oxo-3-phenyl-2-[(pyrazinylcarbonyl)amino]propyl]amino]-butyl]boronic acid
- N-((1R)-1-(DIHYDROXYBORYL)-3-methylbutyl)-N-(pyrazin-2-ylcarbonyl)-L-phenylalaninamide
- (R)-3-methyl-1-((S)-3-phenyl-2-(pyrazine-2-carboxamido)propanamido)butylboronic acid
- NCI60_029010
- Bortezomib (Velcade,MG-341,PS-341)?
- ((R)-3-methyl-1-((S)-3-phenyl-2-(pyrazine-2-carboxamido)propanamido)butyl)boronicacid
- CS-1039
- BORTEZOMIB [INN]
- [(1R)-3-methyl-1-({(2S)-3-phenyl-2-[(pyrazin-2-ylcarbonyl)amino]propanoyl}amino)butyl]boronic acid
- NSC681239
- NSC 681239
- 3mg0
- BORTEZOMIB [VANDF]
- [(1R)-3-methyl-1-[(2S)-3-phenyl-2-[(pyrazin-2-yl)formamido]propanamido]butyl]boronic acid
- CAS-179324-69-7
- DTXCID1020980
- 179324-69-7
- BORTEZOMIB [ORANGE BOOK]
- CHEMBL325041
- Bortexomib
- MLN-341
- BORTEZOMIB [MI]
- DTXSID3040980
- BORTEZOMIB [MART.]
- EX-A8373
- N-((1S)-1-benzyl-2-(((1R)-1-(dihydroxyboranyl)-3-methylbutyl)amino)2-oxoethylpyrazinecarboxamide
- Bortezomib for Injection
- BORTEZOMIB HYDRATE [JAN]
- NCGC00242506-02
- bortezomibum
- Bortezomib [USAN]
- SMR003500787
- MG 341
- AB01273951-02
- Bortezomib- Bio-X
- Bortezomib hydrate
- N-((1R)-1-(dihydroxyboranyl)-3-methylbutyl)-N(alpha)-(pyrazin-2-ylcarbonyl)-L-phenylalaninamide
- UNII-69G8BD63PP
- N-((1S)-1-Benzyl-2-(((1R)-1-(dihydroxyboranyl)-3-methylbutyl)amino)-2-oxoethyl)pyrazinecarboxamide
- Q419319
- LDP 341
- (R)-3-METHYL-1-((S)-3-PHENYL-2-(PYRAZINE-2-CARBOXAMIDO)PROPANAMIDO)BUTAN-2-YLBORONIC ACID
- Tox21_112630
- C19H25BN4O4
- Tox21_112672_1
- BRD-K88510285-001-17-8
- B5741
- ((1R)-3-Methyl-1-(((2S)-3-phenyl-2-((pyrazinylcarbonyl)amino)propanoyl)amino)butyl)boronic acid
- Bortezomib,Velcade
- BORTEZOMIB [EMA EPAR]
- [(1R)-3-Methyl-1-[[(2S)-3-phenyl-2-[(pyrazinylcarbonyl)amino]propanoyl]amino]butyl]boronic acid
- AS-15721
- BORTEZOMIB [WHO-DD]
- Z2213886907
- PROSCRIPT BORONIC ACID
- GTPL6391
- NCGC00181022-01
- Boronic acid, (3-methyl-1-((1-oxo-3-phenyl-2-((pyrazinylcarbonyl)amino)propyl)amino)butyl)-, (S-(R*,S*))-
- BRD-K88510285-001-02-0
- AB01273951_03
- NS00006197
- Pyz-Phe-boroLeu
- BORTEZOMIB [HSDB]
- BRD-K88510285-001-11-1
- HSDB 7666
- LPD 341
- Tox21_112672
- PS-341 [Bortezomib]
- NCGC00242506-06
- NCGC00242506-01
- (R)-3-methyl-1-((S)-3-phenyl-2-(pyrazine-6-carboxamido)propanamido)butylboronic acid
- 1610526-91-4
- Boronic acid, ((1R)-3-methyl-1-(((2S)-1-oxo-3-phenyl-2-((pyrazinylcarbonyl)amino)propyl)amino)butyl)-
- BDBM50069989
- DB00188
- Bortezomib (JAN/USAN/INN)
- CCG-268449
- SR-01000939863
- MFCD09056737
- N-[(1R)-1-(dihydroxyboranyl)-3-methylbutyl]-Nalpha-(pyrazin-2-ylcarbonyl)-L-phenylalaninamide
- SCHEMBL192129
- N-[(1R)-1-(dihydroxyboranyl)-3-methylbutyl]-N(alpha)-(pyrazin-2-ylcarbonyl)-L-phenylalaninamide
- AKOS015909706
- Velcade (TN)
- BB164258
- NCGC00168751-01
- BRD-K88510285-001-18-6
- LPD-341
-
- MDL: MFCD27978443
- Inchi: 1S/C19H25BN4O4/c1-13(2)10-17(20(27)28)24-18(25)15(11-14-6-4-3-5-7-14)23-19(26)16-12-21-8-9-22-16/h3-9,12-13,15,17,27-28H,10-11H2,1-2H3,(H,23,26)(H,24,25)/t15-,17-/m0/s1
- InChI Key: GXJABQQUPOEUTA-RDJZCZTQSA-N
- SMILES: CC(C[C@H](NC([C@@H](NC(C1=CN=CC=N1)=O)CC1=CC=CC=C1)=O)B(O)O)C
Computed Properties
- Exact Mass: 384.19700
- Monoisotopic Mass: 384.197
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 4
- Hydrogen Bond Acceptor Count: 6
- Heavy Atom Count: 28
- Rotatable Bond Count: 9
- Complexity: 500
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 2
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 124
Experimental Properties
- Color/Form: Powder
- Density: 1.214
- Melting Point: 139-143°C
- Boiling Point: 684.30° C
- Flash Point: No data available
- Refractive Index: 1.56
- Solubility: Soluble in chloroform, dimethyl sulfoxide, ethanol and methanol.
- Stability/Shelf Life: Hygroscopic and Moisture Sensitive
- PSA: 124.44000
- LogP: 1.56230
Bortezomib Security Information
- Signal Word:Warning
- Hazard Statement: H300; H310; H330; H372
- Warning Statement: P260; P284; P301+P310; P304+P340; P320; P330; P361; P302+P350; P405; P501
- Hazardous Material transportation number:3261
- Hazard Category Code: 23/24/25-48/23/24/25
- Safety Instruction: S26-S36/37/39
- RTECS:ED7771666
-
Hazardous Material Identification:
- Risk Phrases:R34
- HazardClass:6.1
- PackingGroup:II
- Storage Condition:4°C, protect from light
Bortezomib Customs Data
- HS CODE:2934999090
- Customs Data:
China Customs Code:
2934999090Overview:
2934999090. Other heterocyclic compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to
Summary:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Bortezomib Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A-DB936-100mg |
Bortezomib |
179324-69-7 | 98%(NMR) | 100mg |
294.0CNY | 2021-08-03 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A-DB936-250mg |
Bortezomib |
179324-69-7 | 98%(NMR) | 250mg |
681.0CNY | 2021-08-03 | |
| Matrix Scientific | 094031-1g |
((R)-3-Methyl-1-((S)-3-phenyl-2-(pyrazine-2-carboxamido)propanamido)butyl)boronic acid, 98% |
179324-69-7 | 98% | 1g |
$360.00 | 2023-09-10 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | B5741-50MG |
Bortezomib |
179324-69-7 | >98.0%(HPLC) | 50mg |
¥490.00 | 2024-04-15 | |
| WU HAN AN JIE KAI Biomedical Technology Co., Ltd. | ajci19530-10mg |
Bortezomib (PS-341) |
179324-69-7 | 98% | 10mg |
¥516.00 | 2023-09-09 | |
| WU HAN AN JIE KAI Biomedical Technology Co., Ltd. | ajci19530-25mg |
Bortezomib (PS-341) |
179324-69-7 | 98% | 25mg |
¥893.00 | 2023-09-09 | |
| WU HAN AN JIE KAI Biomedical Technology Co., Ltd. | ajci19530-100mg |
Bortezomib (PS-341) |
179324-69-7 | 98% | 100mg |
¥1964.00 | 2023-09-09 | |
| WU HAN AN JIE KAI Biomedical Technology Co., Ltd. | ajci19530-500mg |
Bortezomib (PS-341) |
179324-69-7 | 98% | 500mg |
¥5352.00 | 2023-09-09 | |
| ChemScence | CS-1039-100mg |
Bortezomib |
179324-69-7 | 99.97% | 100mg |
$180.0 | 2022-04-27 | |
| ChemScence | CS-1039-250mg |
Bortezomib |
179324-69-7 | 99.97% | 250mg |
$71.0 | 2021-09-02 |
Bortezomib Suppliers
Bortezomib Related Literature
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Chorom Pak,Natalie S. Callander,Edmond W. K. Young,Benjamin Titz,KyungMann Kim,Sandeep Saha,Kenny Chng,Fotis Asimakopoulos,David J. Beebe,Shigeki Miyamoto Integr. Biol. 2015 7 643
-
Choong Kim,Junichi Kasuya,Jessie Jeon,Seok Chung,Roger D. Kamm Lab Chip 2015 15 301
-
Sabrina Touchet,Fran?ois Carreaux,Bertrand Carboni,Alexandre Bouillon,Jean-Luc Boucher Chem. Soc. Rev. 2011 40 3895
-
Vilmos Csizmadia,Paul Hales,Christopher Tsu,Jingya Ma,Jiejin Chen,Pooja Shah,Paul Fleming,Joseph J. Senn,Vivek J. Kadambi,Larry Dick,Francis S. Wolenski Toxicol. Res. 2016 5 1619
-
Melissa Ann Gr?wert,Michael Groll Chem. Commun. 2012 48 1364
Additional information on Bortezomib
The Role and Recent Advancements of Bortezomib (CAS No: 179324-69-7) in Modern Medicine
Bortezomib, chemically designated as N-phenylmaleoyl-L-leucine amide, is a groundbreaking compound with the CAS number 179324-69-7. This proteasome inhibitor has revolutionized the treatment of multiple myeloma and has become a cornerstone in the management of certain hematologic malignancies. Its mechanism of action, targeting the ubiquitin-proteasome system, has opened new avenues in cancer therapy and continues to be a subject of extensive research.
The development of Bortezomib marked a significant milestone in the field of oncology. By specifically inhibiting the 26S proteasome, it disrupts the degradation of proteins that are essential for cancer cell survival, leading to apoptosis and growth inhibition. This targeted approach has demonstrated remarkable efficacy in clinical trials, particularly in patients with relapsed or refractory multiple myeloma. The compound's approval by regulatory agencies such as the FDA and EMA underscores its therapeutic potential and safety profile.
Recent studies have expanded the therapeutic applications of Bortezomib beyond multiple myeloma. Research indicates that it may also be effective in treating other hematologic malignancies, including mantle cell lymphoma and acute promyelocytic leukemia. The compound's ability to modulate the tumor microenvironment and enhance immune responses has been a focus of interest. Preclinical studies have shown promising results when Bortezomib is combined with immunotherapy agents, suggesting a synergistic effect that could improve patient outcomes.
The pharmacokinetic profile of Bortezomib is another area of active investigation. Its oral bioavailability and rapid clearance necessitate specific dosing regimens to maintain therapeutic levels. Advances in formulation technology have led to the development of more stable and bioavailable derivatives, improving patient compliance and efficacy. These innovations highlight the ongoing efforts to optimize the delivery and efficacy of this critical therapeutic agent.
One of the most significant challenges in Bortezomib therapy is the development of resistance. Cancer cells can adapt to evade its effects, leading to treatment failure. Understanding these mechanisms is crucial for developing strategies to overcome resistance. Recent research has identified several pathways that contribute to resistance, including mutations in proteasome subunits and upregulation of survival signaling pathways. Targeting these pathways in combination with Bortezomib could mitigate resistance and improve long-term treatment outcomes.
The role of Bortezomib in personalized medicine is also gaining traction. Genomic profiling can help identify patients who are more likely to benefit from this therapy or those at higher risk of developing adverse effects. By tailoring treatment regimens based on individual patient profiles, clinicians can maximize therapeutic benefits while minimizing risks. This approach aligns with the broader goals of precision medicine, where treatments are customized to individual patients' unique biological characteristics.
Future research directions for Bortezomib include exploring its potential in solid tumors and other non-hematologic malignancies. Preliminary studies suggest that its mechanism of action may be applicable to a wider range of cancers. Additionally, investigating its interactions with other therapeutic agents could lead to novel combination therapies that enhance efficacy and reduce toxicity.
The impact of Bortezomib extends beyond its direct therapeutic effects. It has paved the way for further research into proteasome inhibition as a therapeutic strategy. This has spurred the development of next-generation proteasome inhibitors with improved pharmacokinetic properties and reduced side effects. These advancements hold promise for addressing unmet medical needs in various cancer types.
In conclusion, Bortezomib (CAS No: 179324-69-7) represents a significant advancement in cancer therapy. Its ability to target cancer cells through inhibition of the ubiquitin-proteasome system has transformed treatment outcomes for patients with multiple myeloma and other hematologic malignancies. Ongoing research continues to uncover new applications and improve its therapeutic potential, making it a cornerstone in modern oncology.
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