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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
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
A105048
Product name
AbacavirSulphate
Packaging
1mg
Price
$60
Updated
2021/12/16
American Custom Chemicals Corporation
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
AK Scientific
Product number
V2105
Product name
Abacavirsulphate
Packaging
100mg
Price
$210
Updated
2021/12/16
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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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ABACAVIR SULFATE Suppliers

Hangzhou Yuhao Chemical Technology Co., Ltd
Tel
0571-82693216
Fax
+86-571-82880190
Email
info@yuhaochemical.com
Country
China
ProdList
6387
Advantage
52
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
71826
Advantage
60
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131957
Advantage
58
Hefei TNJ Chemical Industry Co.,Ltd.
Tel
+86-0551-65418684 +8618949823763
Fax
0086-551-65418684
Email
sales@tnjchem.com
Country
China
ProdList
25356
Advantage
58
Dideu Industries Group Limited
Tel
+86-29-89586680 +86-15129568250
Email
1026@dideu.com
Country
China
ProdList
20284
Advantage
58
AFINE CHEMICALS LIMITED
Tel
+86-0571-85134551
Fax
008657185134895
Email
sales@afinechem.com
Country
China
ProdList
15109
Advantage
58
Beijing Qinling Pharmaceutical Co., Ltd.
Tel
010-61241352 18901327973
Email
834537306@qq.com
Country
China
ProdList
5860
Advantage
58
Pushan Industry (Shaanxi) Co., Ltd.
Tel
029-81310890 13571859809
Email
info@pushanshiye.com
Country
China
ProdList
9953
Advantage
58
Shanghai Beiwanta Biotechnology Co., Ltd.
Tel
021-67187366 19901745723
Email
info@bwtlab.com
Country
China
ProdList
9650
Advantage
58
SHANGHAI ZZBIO CO., LTD.
Tel
15102117276 19921389125
Email
tech@zzbioco.com
Country
China
ProdList
12064
Advantage
58
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View Lastest Price from ABACAVIR SULFATE manufacturers

Dideu Industries Group Limited
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

136777-48-5, ABACAVIR SULFATERelated Search:


  • ABACAVIR SULPHATE
  • ((1S,4R)-4-(2-amino-6-(cyclopropylamino)-9H-purin-9-yl)cyclopent-2-enyl)methano
  • Abacavir & Abacavir Sulfate
  • Abacavir (hydrochloride)
  • (1S-cis)-4-[2-Amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol monohydrochloride
  • ZIAGEN
  • (4S)-4-[2-amino-6-(cyclopropylamino)purin-9-yl]cyclopenten-1-yl]methanol,sulfuricaci
  • 136777-48-5
  • C14H18N6OHCl