Telaprevir
- CAS No.
- 402957-28-2
- Chemical Name:
- Telaprevir
- Synonyms
- Incivek;CS-61;VX-950;MP-424;CS-1855;LY-570310;elaprevir;Telaprevir;tellaprevir;Telaprevir-d4
- CBNumber:
- CB41519837
- Molecular Formula:
- C36H53N7O6
- Molecular Weight:
- 679.85
- MDL Number:
- MFCD11616089
- MOL File:
- 402957-28-2.mol
- MSDS File:
- SDS
| Melting point | 116-123°C |
|---|---|
| Density | 1.25 |
| storage temp. | Sealed in dry,Store in freezer, under -20°C |
| solubility | Chloroform, Methanol (Slightly) |
| pka | 11.84±0.20(Predicted) |
| form | Solid |
| color | Pale Yellow to Light Yellow |
| FDA UNII | 655M5O3W0U |
| NCI Drug Dictionary | Incivek |
| ATC code | J05AP02 |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS08 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Warning | |||||||||
| Hazard statements | H361fd | |||||||||
| Precautionary statements | P201-P202-P280-P308+P313-P405-P501 | |||||||||
| Safety Statements | 24/25 | |||||||||
| HS Code | 29339900 | |||||||||
| NFPA 704 |
|
Telaprevir price More Price(43)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | SML2654 | Telaprevir ≥90% (HPLC) | 402957-28-2 | 5MG | $64.6 | 2024-03-01 | Buy |
| Sigma-Aldrich | SML2654 | Telaprevir ≥90% (HPLC) | 402957-28-2 | 25MG | $209 | 2024-03-01 | Buy |
| Cayman Chemical | 20054 | Telaprevir | 402957-28-2 | 5mg | $74 | 2024-03-01 | Buy |
| Cayman Chemical | 20054 | Telaprevir | 402957-28-2 | 10mg | $105 | 2024-03-01 | Buy |
| Cayman Chemical | 20054 | Telaprevir | 402957-28-2 | 25mg | $238 | 2024-03-01 | Buy |
Telaprevir Chemical Properties,Uses,Production
Description
The hepatitis C virus (HCV) protease inhibitor telaprevir (VX-950, MP- 424,LY-570310) was approved by the U.S. FDA in May 2011 for the treatment of genotype 1 chronic HCV infection in adult patients in combination with peginterferon alfa and ribavirin (PR). Telaprevir and boceprevir (vide supra) are the first two HCV protease inhibitors to be approved for treatment of HCV infection. Telaprevir is a HCV NS3-4A protease inhibitor that exerts its antiviral effect by blocking the release of nonstructural viral proteins from a polyprotein precursor. Telaprevir is a potent inhibitor of the protease (IC50=10 nM) and is active in cell culture (HCV 1b replicon assay, EC50=354 nM). Telaprevir was identified from efforts to truncate a decamer peptide inhibitor derived from the natural substrate NS5A-5B and was guided by structure-based design. The ketoamide group of telaprevir forms a covalent, reversible bond with the active site serine hydroxyl of the protease and compensates for the loss of affinity resulting from truncation of the peptide. Despite the presence of the reactive keto-amide group, telaprevir is >500-fold less potent against other serine proteases. Synthesis of the key octahydrocyclopenta[c]pyrrole-1-carboxylic acid fragment of telaprevir is achieved by a-deprotonation of Boc-protected 3-azabicyclo[3.3.0]nonane followed by reaction with CO2 and resolution of the racemic acid. Alternatively, deprotonation is carried out in the presence of a chiral amine to give the enantiomerically enriched acid.
Chemical Properties
Telaprevir is White Solid
Originator
Eli Lilly (United States)
Uses
Labeled Telaprevir, intended for use as an internal standard for the quantification of Telaprevir by GC- or LC-mass spectrometry.
Uses
A labelled peptidomimetic inhibitor of hepatitis C virus protease.
Uses
Telaprevir is a peptidomimetic inhibitor of hepatitis C virus protease.
Definition
ChEBI: An oligopeptide consisting of N-(pyrazin-2-ylcarbonyl)cyclohexylalanyl, 3-methylvalyl, octahydrocyclopenta[c]pyrrole-1-carboxy, and 3-amino-N-cyclopropyl-2-oxohexanamide residues joined in sequence. Used f r treatment of chronic hepatitis C virus genotype 1 infection.
brand name
Incivek
Clinical Use
Telaprevir is a potent peptide mimetic inhibitor of Hepatitis C virus (HCV) and works via covalent reversible binding to the NSV-3A protease enzyme. Telaprevir was discovered and developed by Vertex pharmaceuticals. The drug is marketed as an oral treatment for HCV infection in combination with Peg interferon and ribavarin for patients who are refractory to the initial standard therapy. The initial SAR studies and the discovery of teleprevir have been published. In addition, a full review of the discovery process that led to the development of telaprevir, including several iterations of the syntheses of teleprevir leading to the process route, has been reported.
Synthesis
For preparation of bulk API, a convergent synthetic strategy
was utilized as described in the scheme. Retrosynthetically the
penultimate intermediate 212, which was coupled with amine
213 for the final step, was prepared by coupling bicyclic amine
217 with amino acids 216 and 215 and then with pyrazine acid
214.
In the early stages of development, the cyclopropyl amide fragment
213 was made using a MCR coupling sequence by reacting
aldehyde 218 with cyclopropyl isocyanide (219) and triflouroacetic
acid to give amide alcohol 220 in 85% yield. Removal
of the Cbz group was accomplished via hydrogenolysis to provide
key cyclopropyl amide alcohol 213 in 95% yield. While this route
was shorter in terms of steps, it was not amenable to large-scale
preparation due to difficulties associated with the handling of isocyanide
219.
Thus, for large-scale synthesis, the route depicted in Scheme 35 was utilized. Commercially available Cbz-protected amino acid 221 was converted to the corresponding Weinreb amide 222 using CDI as the activating agent. This was followed by LAH reduction to give aldehyde 218 in 73% yield from 221. Aldehyde 218 was reacted with sodium cyanide under neutral to mildly basic conditions allowing for easy workup of the cyanohydrin, which was immediately hydrolyzed by refluxing in 4 N hydrochloric acid in dioxane to deliver hydroxy acid HCl salt 223. Since the formation of the acyloin resulted in removal of the Cbz protecting group, reinstallation of this protecting group preceded conventional amide bond formation through the intermediacy of the succinate ester of 224. This provided the desired amide alcohol 220 in 56% yield from 223. Hydrogenolysis of Cbz carbamate 220 then furnished the requisite intermediate amine (213) in 73% yield.
The large-scale synthesis of bicyclic pyrrolidine 231 was accomplished as described in the following scheme. Commercially available 3-azabicyclo[ 3.3.0]nonane hydrochloride (225) was first protected as the corresponding Boc carbamate 226 in 90% yield. Deprotonation of the bicyclic pyrrolidine carbamate 226 with sec-BuLi and sequential quench with bubbling carbon dioxide gas followed by sodium hydrogensulfate resulted in racemic acid 227 in 80% yield. Racemate 227 was resolved using (S)-tetrahydronapthalamine (228) in ethyl acetate and isopropanol at 70¨C75??C. This mixture was allowed to cool down slowly to effect the crystallization of the optically enriched chiral salt 229 in 83% yield with greater than 99.5% ee. This enatioenriched salt was free based with sodium hydrogen sulfate and converted to t-butyl ester 230 using Boc anhydride and DMAP. The secondary amine of 230 was liberated using methane sulfonic acid at room temperature followed by salt formation with oxalic acid in isopropyl acetate to give oxalic acid salt 231 in 81% yield over 3 steps.
With the synthesis of the key intermediates complete, sequential coupling events were then executed to complete the synthesis of teleprevir (following scheme). Fragment 217 was coupled with the Cbz-protected valine (216) using EDCI and HOBt to give intermediate 232 in 87% yield. Similarly, after removal of the Cbz group of 232 via catalytic hydrogenolysis, the resulting amine was coupled with cyclohexyl amino acid 215 to give dipeptide intermediate 233 in 89% yield over 2 steps. Sequential cleavage of the Cbz group in 233 followed by CDI-mediated coupling with commercially available pyrazine acid 214 gave rise to the expected pyrazine amide intermediate. Subsequent hydrolysis of the t-butyl ester through the use of concentrated acid in DCM provided the key intermediate tripeptidic acid (212) in 68% over 3 steps. The tripeptide 212 was then coupled with cyclopropyl amide amine 213 using EDCI, HOBt and N-methyl morpholine (NMM) to provide penultimate intermediate alcohol 234 in 95% yield. Subjection of 234 to Dess¨CMartin periodinane (DMP) oxidation in t-butanol and DCM furnished telaprevir (XXI) in 85% yield.
Drug interactions
Potentially hazardous interactions with other drugs
Alpha-blockers: avoid with alfuzosin.
Analgesics: risk of ventricular arrhythmias with
methadone.
Anti-arrhythmics: risk of ventricular arrhythmias
with amiodarone and disopyramide - avoid; risk
of ventricular arrhythmias with flecainide andpropafenone - use with caution; use IV lidocaine
with caution.
Antibacterials: concentration of both drugs increased
with clarithromycin, erythromycin and telithromycin,
increased risk of ventricular arrhythmias; avoid with
rifabutin and rifampicin (concentration significantly
reduced by rifampicin).
Anticoagulants: concentration of warfarin possibly
affected; avoid with apixaban; possibly increased
dabigatran concentration.
Antidepressants: possibly increased trazodone
concentration; avoid with St John’s wort.
Antiepileptics: avoid with carbamazepine,
fosphenytoin, phenobarbital, phenytoin and
primidone.
Antifungals: concentration of both drugs possibly
increased with ketoconazole, increased risk
of ventricular arrhythmias; possibly increased
itraconazole concentration; possibly increased
posaconazole concentration - increased risk of
ventricular arrhythmias; possibly altered voriconazole
concentration - increased risk of ventricular
arrhythmias.
Antipsychotics: avoid with pimozide; possibly
increases lurasidone and quetiapine concentration -
avoid.
Antivirals: concentration possibly reduced by
atazanavir; concentration of atazanavir possibly
increased; avoid with darunavir, fosamprenavir and
lopinavir; concentration of daclatasvir and possibly
olaparib increased - reduce daclatasvir and olaparib
dose; concentration reduced by efavirenz - increase
telaprevir dose; concentration possibly reduced
by ritonavir; concentration of tenofovir possibly
increased.
Anxiolytics and hypnotics: possibly increased
midazolam concentration - risk of prolonged
sedation, avoid concomitant use with oral
midazolam.
Beta-blockers: risk of ventricular arrhythmias with
sotalol - avoid.
Ciclosporin: concentration of both drugs increased,
reduce ciclosporin dose.
Cilostazol: possibly increases cilostazol
concentration.
Colchicine: possibly increased risk of colchicine
toxicity - suspend or reduce colchicine dose, avoid in
hepatic or renal impairment.
Cytotoxics: possibly increases bosutinib
concentration - avoid or consider reducing dose of
bosutinib; reduce dose of ruxolitinib.
Domperidone: possibly increased risk of ventricular
arrhythmias - avoid.
Ergot alkaloids: avoid concomitant use.
Guanfacine: possibly increases guanfacine dose -
halve dose of guanfacine.
Lipid-regulating drugs: avoid with lomitapide,
simvastatin and atorvastatin.
Oestrogens: possibly reduced ethinylestradiol
concentration and contraceptive effect.
Sildenafil: avoid concomitant use.
Sirolimus: concentration of both drugs increased,
reduce sirolimus dose.
Beta2
sympathomimetics: avoid with salmeterol - risk
of ventricular arrhythmias.
Tacrolimus: concentration of both drugs increased,
reduce tacrolimus dose.
Tadalafil: avoid with high dose tadalafil.
Vardenafil: avoid concomitant use.
Metabolism
Extensively metabolised in the liver, involving hydrolysis,
oxidation, and reduction.
Multiple metabolites were detected in faeces, plasma and
urine.
storage
Store at -20°C
Telaprevir Preparation Products And Raw materials
Raw materials
Preparation Products
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Alpha Biopharmaceuticals Co., Ltd | +86-15542445688 | sales@alabiochem.com | China | 888 | 58 |
| Capot Chemical Co.,Ltd. | +86-（0）57185586718 +86-13336195806 | sales@capot.com | China | 29791 | 60 |
| Beijing Cooperate Pharmaceutical Co.,Ltd | 010-60279497 | sales01@cooperate-pharm.com | CHINA | 1803 | 55 |
| Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 | info@tianfuchem.com | China | 21634 | 55 |
| Hangzhou FandaChem Co.,Ltd. | +8615858145714 | FandaChem@Gmail.com | China | 9210 | 55 |
| Shanghai Yingrui Biopharma Co., Ltd. | +86-21-33585366 - 03@ | sales03@shyrchem.com | CHINA | 738 | 60 |
| ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 | ivan@atkchemical.com | China | 32957 | 60 |
| career henan chemical co | +86-0371-86658258 +8613203830695 | sales@coreychem.com | China | 29882 | 58 |
| Biochempartner | 0086-13720134139 | candy@biochempartner.com | CHINA | 965 | 58 |
| Hubei xin bonus chemical co. LTD | 86-13657291602 | linda@hubeijusheng.com | CHINA | 22963 | 58 |
View Lastest Price from Telaprevir manufacturers
| Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
|---|---|---|---|---|---|---|---|---|
 |
2023-06-26 | Telaprevir
402957-28-2
|
US $200.00 / kg | 1kg | 99% | 1000kg/Month | Hebei Mingeng Biotechnology Co., Ltd | |
 |
2023-04-11 | Telaprevir (VX-950)
402957-28-2
|
US $100.00 / g | 10g | 99% | 1000g | Shijiazhuang Gantuo Biotechnology Co., Ltd | |
 |
2023-01-31 | Telaprevir
402957-28-2
|
US $0.00 / KG | 1KG | 99% | 50000KG/month | Hebei Mojin Biotechnology Co., Ltd |
-
- Telaprevir
402957-28-2
- US $200.00 / kg
- 99%
- Hebei Mingeng Biotechnology Co., Ltd
-
- Telaprevir (VX-950)
402957-28-2
- US $100.00 / g
- 99%
- Shijiazhuang Gantuo Biotechnology Co., Ltd
-
- Telaprevir
402957-28-2
- US $0.00 / KG
- 99%
- Hebei Mojin Biotechnology Co., Ltd