Cobicistat
Description In vitro- Product Name
- Cobicistat
- CAS No.
- 1004316-88-4
- Chemical Name
- Cobicistat
- Synonyms
- Tybost;Cobicistat (GS-9350);GS9350;CS-753;GS 9350;GS-9350;Genvoya.;Cobicistat;Cobiclstat;Cobicistat D8
- CBNumber
- CB62627692
- Molecular Formula
- C40H53N7O5S2
- Formula Weight
- 776.02
- MOL File
- 1004316-88-4.mol
Cobicistat Property
- Melting point:
- 50-54°C
- Boiling point:
- 974.5±65.0 °C(Predicted)
- Density
- 1.228±0.06 g/cm3 (20 ºC 760 Torr)
- storage temp.
- Hygroscopic, Refrigerator, under inert atmosphere
- solubility
- Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 11.86±0.46(Predicted)
- color
- White to Off-White
- Stability:
- Hygroscopic
- InChI
- InChI=1S/C40H53N7O5S2/c1-29(2)38-43-34(27-53-38)25-46(3)39(49)45-36(16-17-47-18-20-51-21-19-47)37(48)42-32(22-30-10-6-4-7-11-30)14-15-33(23-31-12-8-5-9-13-31)44-40(50)52-26-35-24-41-28-54-35/h4-13,24,27-29,32-33,36H,14-23,25-26H2,1-3H3,(H,42,48)(H,44,50)(H,45,49)/t32-,33-,36+/m1/s1
- InChIKey
- ZCIGNRJZKPOIKD-CQXVEOKZSA-N
- SMILES
- C(OCC1SC=NC=1)(=O)N[C@@H](CC1=CC=CC=C1)CC[C@H](CC1=CC=CC=C1)NC(=O)[C@H](CCN1CCOCC1)NC(=O)N(C)CC1=CSC(C(C)C)=N1
N-Bromosuccinimide Price
- Product number
- 23433
- Product name
- Cobicistat
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $37
- Updated
- 2024/03/01
- Product number
- 23433
- Product name
- Cobicistat
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $151
- Updated
- 2024/03/01
- Product number
- 26442
- Product name
- Cobicistat-d8
- Purity
- ≥99% deuterated forms (d<sub>1</sub>-d<sub>8</sub>)
- Packaging
- 1mg
- Price
- $922
- Updated
- 2023/01/06
- Product number
- 23433
- Product name
- Cobicistat
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $266
- Updated
- 2024/03/01
- Product number
- 23433
- Product name
- Cobicistat
- Purity
- ≥98%
- Packaging
- 25mg
- Price
- $573
- Updated
- 2024/03/01
Cobicistat Chemical Properties,Usage,Production
Description
Cobicistat (GS-9350) is a potent and selective inhibitor of CYP3A with IC50 of 30-285 nM.
In vitro
Cobicistat (GS-9350) is a potent, and selective inhibitor of human cytochrome P450 3A (CYP3A) enzymes as a pharmacoenhancer. GS-9350 inhibits CYP3A with IC50 spectrum from 30 nM to 285 nM. In contrast to ritonavir, GS-9350 is devoid of anti-HIV activity, with IC50 of > 30μM against HIV-1 protease and EC50 of > 30μM in MT-2 HIV infection assay, and is thus more suitable for use in boosting anti-HIV drugs without risking selection of potential drug-resistant HIV variants. GS-9350 shows reduced liability for drug interactions and may have potential improvements in tolerability over ritonavir.
Description
Cobicistat, a selective, mechanism-based CYP3A inhibitor, was discovered and developed by Gilead Sciences, Inc. In 2013, European Medicines Agency (EMA) approved cobicistat (Tybost) for the treatment of HIV-1 infection in combination with protease inhibitors (PIs) atazanavir or darunavir. Interestingly, cobicistat does not interact with HIV directly, but instead serves as a pharmacokinetic enhancer to boost the anti-HIV effect of atazanavir or darunavir through blockade of CYP3A. Cobicistat slows CYP-mediated metabolism of atazanavir and darunavir, resulting in prolonged systemic exposure of the drug(s). Cobicistat is also available as part of a fixed-dose combination tablet (Stribild) of four additional drugs with CYP3A liabilities (elvitegravir, cobicistat, emtricitabine and tenofovir disoproxil fumarate), which was approved in U.S. in 2012, and subsequently approved in Europe and Japan in 2013.
Originator
Gilead (United States)
Uses
Cobicistat is a HIV protease inhibitor and have been coadministered with low-dose ritonavir (R535000) as a pharmacoenhancer, significantly increasing their plasma concentrations.
Uses
Isotope labelled analogue of Cobicistat (C633150), a HIV protease inhibitor and have been coadministered with low-dose ritonavir (R535000) as a pharmacoenhancer, significantly increasing their plasma concentrations.
Uses
Antiretroviral;Labeled Cobicistat, intended for use as an internal standard for the quantification of Cobicistat by GC- or LC-mass spectrometry.
Definition
ChEBI: Cobicistat is a monocarboxylic acid amide obtained by formal condensation of the carboxy group of (2S)-2-({[(2-isopropyl-1,3-thiazol-4-yl)methyl](methyl)carbamoyl}amino)-4-(morpholin-4-yl)butanoic acid with the amino group of 1,3-thiazol-5-ylmethyl [(2R,5R)-5-amino-1,6-diphenylhexan-2-yl]carbamate. Acts as a pharmacoenhancer in treatment of HIV-1 by inhibiting P450 enzymes that metabolise other medications.. It has a role as a P450 inhibitor. It is a member of 1,3-thiazoles, a member of morpholines, a member of ureas, a carbamate ester and a monocarboxylic acid amide.
brand name
Tybost
Clinical Use
Pharmacokinetic enhancer used to increase the effect of atazanavir and darunavir
Synthesis
Commercial L-methionine (24) was treated with bromoacetic acid at elevated temperatures to afford aminolactone salt 25 in 70% yield. This material was then reacted with methyl aminomethylthiazole (26) in the presence of CDI and diisopropylethylamine to arrive at urea 27 in 91% yield. Next, lactone 27 underwent a ring-opening sequence upon exposure to trimethylsilyl iodide (TMSI) giving intermediate 28. The iodide was then displaced by morpholine, followed by treatment with oxalic acid to deliver the L-thiazole morpholine ethyl ester as the oxalate salt 29 in 71% yield for the sequence. Base-mediated hydrolysis of ethyl ester 29, followed by treatment of carboxylate 30 with mono-carbonate hydrochloride 31 in the presence of EDCI and HOBT, provided cobicistat (V) in 76% yield for two steps.
Drug interactions
Potentially hazardous interactions with other drugsAlpha-blockers: concentration of alfuzosin possibly
increased - avoid.
Anti-arrhythmics: concentration of amiodarone
possibly increased - avoid.
Antibacterials: concentration reduced by rifabutin
and rifampicin - adjust cobicistat dose, avoid with
rifampicin.
Anticoagulants: avoid with apixaban; anticoagulant
effect of rivaroxaban possibly enhanced - avoid.
Antidepressants: concentration possibly reduced by
St John’s wort - avoid.
Antiepileptics: concentration of cobicistat
possibly reduced by carbamazepine, fosphenytoin
phenobarbital, phenytoin and primidone - avoid.
Antifungals: concentration of itraconazole and
ketoconazole possibly increased - reduce antifungal
dose.
Antipsychotics: concentration of lurasidone and
pimozide possibly increased - avoid.
Antivirals: concentration of daclatasvir and
maraviroc possibly increased - reduce daclatasvir
and maraviroc dose; avoid with dasabuvir, nevirapine,
ombitasvir, paritaprevir, ritonavir and simeprevir;
concentration of elbasvir and grazoprevir increased -
avoid; concentration of olaparib possibly increased -
avoid or reduce olaparib dose; concentration of both
drugs reduced with tipranavir - avoid.
Anxiolytics: avoid with oral midazolam.
Avanafil: concentration of avanafil possibly increased
- avoid.
Bosentan: avoid concomitant use.
Cardiac glycosides: concentration of digoxin possibly
increased - reduce initial dose of digoxin.
Corticosteroids: concentration of corticosteroids
possibly increased avoid or use with caution.
Cytotoxics: concentration of ibrutinib possibly
increased - reduce ibrutinib dose; concentration of
olaparib possibly increased - avoid or reduce dose of
olaparib.
Domperidone: possible increased risk of ventricular
arrhythmias - avoid.
Ergot alkaloids: concentration of ergot alkaloids
possibly increased - avoid.
Immunosuppression: concentration of ciclosporin,
sirolimus and tacrolimus possibly increased.
Lipid-lowering drugs: concentration of atorvastatin
possibly increased - reduce atorvastatin dose; avoid
with simvastatin.
Oestrogens: metabolism of oestrogens accelerated,
reduced contraceptive effect - avoid or use with
caution.
Salmeterol: avoid concomitant use.
Sildenafil: concentration of sildenafil possibly
increased - avoid sildenafil for pulmonary arterial
hypertension, reduce dose for erectile dysfunction.
Tadalafil: concentration of tadalafil possibly
increased - reduce dose of tadalafil.
Vardenafil: concentration of vardenafil possibly
increased - reduce dose of vardenafil.
Metabolism
Cobicistat is metabolised via CYP3A (major)- and
CYP2D6 (minor)-mediated oxidation. Following oral
administration of [14C]-cobicistat, 99% of circulating
radioactivity in plasma was unchanged cobicistat. Low
levels of metabolites are observed in urine and faeces and
do not contribute to the CYP3A inhibitory activity of
cobicistat.
Following oral administration of [14C]-cobicistat, 86%
and 8.2% of the dose were recovered in faeces and urine,
respectively.
References
[1] deeks ed. cobicistat: a review of its use as a pharmacokinetic enhancer of atazanavir and darunavir in patients with hiv-1 infection. drugs. 2014 feb;74(2):195-206.
Cobicistat Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from Cobicistat manufacturers
- Product
- Cobicistat 1004316-88-4
- Price
- US $2063.00/g
- Min. Order
- 1g
- Purity
- 99
- Supply Ability
- 1kg
- Release date
- 2021-06-04
- Product
- Cobicistat 1004316-88-4
- Price
- US $0.00-0.00/KG
- Min. Order
- 1KG
- Purity
- 98%
- Supply Ability
- 1Ton
- Release date
- 2022-10-13
- Product
- Cobicistat 1004316-88-4
- Price
- US $15.00-10.00/KG
- Min. Order
- 1KG
- Purity
- 99%+ HPLC
- Supply Ability
- Monthly supply of 1 ton
- Release date
- 2021-07-10