ABACAVIR SULFATE
- Product Name
- ABACAVIR SULFATE
- CAS No.
- 136777-48-5
- Chemical Name
- ABACAVIR SULFATE
- Synonyms
- ZIAGEN;ABACAVIR SULPHATE;Abacavir (hydrochloride);Abacavir & Abacavir Sulfate;((1S,4R)-4-(2-amino-6-(cyclopropylamino)-9H-purin-9-yl)cyclopent-2-enyl)methano;(4S)-4-[2-amino-6-(cyclopropylamino)purin-9-yl]cyclopenten-1-yl]methanol,sulfuricaci;(1S-cis)-4-[2-Amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol monohydrochloride
- CBNumber
- CB5425547
- Molecular Formula
- C14H19ClN6O
- Formula Weight
- 322.8
- MOL File
- 136777-48-5.mol
N-Bromosuccinimide Price
- Product number
- A105048
- Product name
- AbacavirSulphate
- Packaging
- 1mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- CCH0005937
- Product name
- 4R-(2-AMINO-6-(CYCLOPROPYLAMINO)-9H-PURIN-9-YL)-2-CYCLOPENTENE-1S-METHANOL, MONOHYDROCHLORIDE
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $181.65
- Updated
- 2021/12/16
- Product number
- V2105
- Product name
- Abacavirsulphate
- Packaging
- 100mg
- Price
- $210
- Updated
- 2021/12/16
ABACAVIR SULFATE Chemical Properties,Usage,Production
Uses
Abacavir hydrochloride is a competitive, orally active nucleoside reverse transcriptase inhibitor. Abacavir hydrochloride can inhibits the replication of HIV. Abacavir hydrochloride shows anticancer activity in prostate cancer cell lines. Abacavir hydrochloride can trespass the blood-brain-barrier and suppresses telomerase activity[1][2][3].
Definition
ChEBI: Abacavir sulfate is an azaheterocycle sulfate salt that is the sulfate salt of the HIV-1 reverse transcriptase inhibitor abacavir. It is functionally related to an abacavir.
in vivo
Abacavir hydrochloride (100 and 200 mg/kg, p.o.; 4 h) dose-dependently promotes thrombus formation[2].
Abacavir hydrochloride (50 mg/kg/d; i.p.; 14 d) with 0.1 mg/kg/d Decitabine.html" class="link-product" target="_blank">Decitabine (HY-A0004) enhances survival of high-risk medulloblastoma-bearing mice[3].
| Animal Model: | Male mice (9-weeks old, 22-30 g) - wild-type (WT) C57BL/6 or homozygous knockout (P2rx7 KO, B6.129P2-P2rx7tm1Gab/J)[2] |
| Dosage: | Route 1: 2.5, 5, and 7.5 μg/mL, 100 μL Route 2: 100 and 200 mg/kg |
| Administration: | Intrascrotal or oral administration for 4 h |
| Result: | Dose-dependently promoted thrombus formation. |
| Animal Model: | NSGTM mice, patient-derived xenograft (PDX) cells of non-WNT/non-SHH, Group 3 and of SHH/ TP53-mutated medulloblastoma[3] |
| Dosage: | 50 mg/kg/d with 0.1 mg/kg/d Decitabine |
| Administration: | Intraperitoneal injection, daily for 14 days |
| Result: | Inhibited tumor growth and enhanced mouse survival. |
References
[1] Carlini F, et al. The reverse transcription inhibitor abacavir shows anticancer activity in prostate cancer cell lines. PLoS One. 2010 Dec 3;5(12):e14221. DOI:10.1371/journal.pone.0014221
[2] Collado-Diaz V, et al. Abacavir Induces Arterial Thrombosis in a Murine Model. J Infect Dis. 2018 Jun 20;218(2):228-233. DOI:10.1093/infdis/jiy001
[3] Gringmuth M, et al. Enhanced Survival of High-Risk Medulloblastoma-Bearing Mice after Multimodal Treatment with Radiotherapy, Decitabine, and Abacavir. Int J Mol Sci. 2022 Mar 30;23(7):3815. DOI:10.3390/ijms23073815
[4] McComsey GA, et al. Improvements in lipoatrophy, mitochondrial DNA levels and fat apoptosis after replacing stavudine with abacavir or zidovudine. AIDS. 2005 Jan 3;19(1):15-23. DOI:10.1097/00002030-200501030-00002
ABACAVIR SULFATE Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from ABACAVIR SULFATE manufacturers
- Product
- ABACAVIR SULFATE 136777-48-5
- Price
- US $1.10/g
- Min. Order
- 1g
- Purity
- 99.9%
- Supply Ability
- 100 Tons Min
- Release date
- 2021-07-15