成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

ChemicalBook--->CAS DataBase List--->1038620-68-6

1038620-68-6

1038620-68-6 Structure

1038620-68-6 Structure
IdentificationBack Directory
[Name]

Purfalcamine
[CAS]

1038620-68-6
[Synonyms]

Purfalcamine
[Molecular Formula]

C29H33FN8O
[MDL Number]

MFCD32857138
[MOL File]

1038620-68-6.mol
[Molecular Weight]

528.62
Chemical PropertiesBack Directory
[Boiling point ]

784.8±70.0 °C(Predicted)
[density ]

1.42±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[form ]

Solid
[pka]

10.41±0.70(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Biological Activity]

Purfalcamine is an orally active and selective inhibitor of Plasmodium falciparum calcium-dependent protein kinase 1 (PfCDPK1) with IC50 of 17 nM and EC50 of 230 nM. It has antimalarial activity and can cause developmental arrest in the schizont stage of Plasmodium.
[in vitro]

Purfalcamine has low activity against Toxoplasma gondii calcium-dependent protein kinase 3 (TgCDPK3).
Purfalcamine (225, 450 nM) has no effect on the parasitemia in the first 32 hours. After about 40 hours, parasite level remains stable and then begins dropping.
Purfalcamine inhibits proliferation with EC 50 s of 171-259 nM for P. falciparum strains (3D7, Dd2, FCB, HB3 and W2), which indicate effectiveness against drug-resistant parasites.
Given that the EC 50 value for P. falciparum (3D7) is 230 nM, Purfalcamine shows a therapeutic window ranging from 23-fold to 36-fold (EC 50 s for CHO=12.33 μM, HEp2=7.235 μM, HeLa=7.029 μM and Huh7 =5.476 μM).

[in vivo]

Purfalcamine (10 mg/kg; oral gavage; BID; for 6 days) demonstrates a delay in the onset of parasitemia in treated mice.
Purfalcamine (20 mg/kg; orally gavage) exhibits a C max of 2.6 μM with a half-life of 3.1 hours.

Animal Model: Male BALB/c mice, 7 weeks of age with the malaria parasite
Dosage: 10 mg/kg
Administration: Oral gavage; BID; for 6 days
Result: Demonstrated a delay in the onset of parasitemia in treated mice when compared with control mice.
Animal Model: Five- to six-week-ol d male Balb/c mice (22-25 g)
Dosage: 20 mg/kg (Pharmacokinetic Analysis)
Administration: Orally gavage
Result: Exhibited a maximum plasma exposure (C max ) of 2.6 μM with a half-life of 3.1 hours.
[storage]

Store at -20°C
1038620-68-6 suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +8613564774135 , +8613564774135
Website:
Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  
Tel: 18149758185 18149758185
Website: www.caerulumpharma.com
Company Name: DC Chemicals  
Tel: 021-58447131 13564518121
Website: http://m.is0513.com/ShowSupplierProductsList927327/0.htm
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Website: http://www.chemegen.com
Company Name: TargetMol Chemicals Inc.  
Tel: 4008200310
Website: https://www.targetmol.cn/
Company Name: Aikon International Limited  
Tel: 18626450290
Website: http://www.aikonchem.com
Company Name: RD International Technology Co., Limited  
Tel: 18024082417
Website: www.ruidiresearch.com
Company Name: MedChemExpress  
Tel: 021-58955995
Website: www.medchemexpress.com
Tags:1038620-68-6 Related Product Information