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

Home Cart Sign in  
Chemical Structure| 1276110-06-5 Chemical Structure| 1276110-06-5
Chemical Structure| 1276110-06-5

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

{[proInfo.proName]}

CAS No.: 1276110-06-5

,{[proInfo.pro_purity]}

HS-173 is a potent PI3Kα inhibitor with IC50 of 0.8 nM.

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support Online Technical Q&A
Product Citations

Alternative Products

Product Details of HS-173

CAS No. :1276110-06-5
Formula : C21H18N4O4S
M.W : 422.46
SMILES Code : O=C(C1=CN=C2C=CC(C3=CC(NS(=O)(C4=CC=CC=C4)=O)=CN=C3)=CN21)OCC
MDL No. :MFCD28023584
InChI Key :SEKOTFCHZNXZMM-UHFFFAOYSA-N
Pubchem ID :52936849

Safety of HS-173

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of HS-173

PI3K-AKT

Isoform Comparison

Biological Activity

Target
  • p110α

    PI3Kα , IC50:0.8 nM

In Vitro:

Cell Line
Concentration Treated Time Description Reference
MG-63 cells 1 nM 1 hour To investigate the effect of HS-173 on Wnt5a/ROR2-mediated cell migration, the results showed that HS-173 significantly inhibited Wnt5a/ROR2-mediated cell migration. PMC5707918
CT26 cells 0.01 μM to 50 μM 24 hours To evaluate the cytotoxicity of PARP and PI3K inhibitor combinations, results showed that the N-H combination significantly enhanced cytotoxicity after radiation. PMC7689338
KB-3-1 2 μM 24 hours HS-173 significantly induced G2/M cell cycle arrest PMC10093605
KB-V1 2 μM 24 hours G2/M arrest induced by HS-173 was significantly reduced PMC10093605
S1 2 μM 24 hours HS-173 significantly induced G2/M cell cycle arrest PMC10093605
S1-MI-80 2 μM 24 hours G2/M arrest induced by HS-173 was significantly reduced PMC10093605
MG-63 cells 1 nM 30 minutes Wnt5a-induced activation of RhoA was mostly blocked by pretreatment of HS-173 in MG-63 cells PMC5310072
U2OS cells 1 nM 30 minutes Wnt5a-induced activation of RhoA was mostly blocked by pretreatment of HS-173 in U2OS cells PMC5310072
CAL 27 cells 0.125 μM 48 hours HS-173 showed anti-proliferative effects and induced apoptosis in CAL 27 cells. PMC10341739
FaDu cells 0.8 μM 48 hours HS-173 showed anti-proliferative effects and induced apoptosis in FaDu cells. PMC10341739
CT26 cells 0.4 μM 6 hours To evaluate the ability of N-H to induce immunogenic cell death, results showed that N-H significantly induced CRT expression. PMC7689338

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description Reference
BALB/c mice CT26 colorectal cancer model Tail vein injection 3.57 mg/kg HS-173, 3.69 mg/kg niraparib Every 2 days, for a total of 3 doses To evaluate the antitumor efficacy of N-H POx in combination with radiotherapy and immunotherapy, results showed that N-H POx significantly enhanced tumor control and increased tumor infiltrating lymphocytes. PMC7689338

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.37mL

0.47mL

0.24mL

11.84mL

2.37mL

1.18mL

23.67mL

4.73mL

2.37mL

References

 

Historical Records

Categories