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  3. LY3177833

LY3177833 

Cat. No.: HY-100023 Purity: 99.76%
COA Handling Instructions

LY3177833 (Example 4) is an orally active CDC7 and pMCM2 inhibitor with IC50 values of 3.3 nM and 290 nM, respectively. LY3177833 is a senescence inducer.

For research use only. We do not sell to patients.

LY3177833 Chemical Structure

LY3177833 Chemical Structure

CAS No. : 1627696-51-8

Size Price Stock Quantity
Solution
10 mM * 1 mL in DMSO USD 145 In-stock
Estimated Time of Arrival: December 31
Solid + Solvent
10 mM * 1 mL
ready for reconstitution
USD 145 In-stock
Estimated Time of Arrival: December 31
Solid
5 mg USD 132 In-stock
Estimated Time of Arrival: December 31
10 mg USD 185 In-stock
Estimated Time of Arrival: December 31
50 mg USD 528 In-stock
Estimated Time of Arrival: December 31
100 mg USD 845 In-stock
Estimated Time of Arrival: December 31
200 mg   Get quote  
500 mg   Get quote  

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Customer Review

Based on 1 publication(s) in Google Scholar

Other Forms of LY3177833:

Top Publications Citing Use of Products
  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

LY3177833 (Example 4) is an orally active CDC7 and pMCM2 inhibitor with IC50 values of 3.3 nM and 290 nM, respectively. LY3177833 is a senescence inducer[1][2].

IC50 & Target[1]

Cdc7

3.3 nM (IC50)

pMCM2

290 nM (IC50)

In Vitro

LY3177833 (10 μM; 4 days) increases SA-β-gal content in Hep3B cells[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[2]

Cell Line: Hep3B cells
Concentration: 10 μM
Incubation Time: 4 days
Result: Increased the expression of human SA-β-gal.
In Vivo

LY3177833 (Example 4; 10.4-31.2 mg/kg; oral gavage; twice a day; for 2 weeks; female athymic Balb/c nude mice with SW620 cells) treatment causes significant tumor regression in a dose-dependent manner. Also, no significant tumor growth is observed for 2 weeks after dosing cessation[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female athymic Balb/c nude mice (5-6 weeks old) with SW620 cells[1]
Dosage: 10.4 mg/kg, 20.8 mg/kg and 31.2 mg/kg
Administration: Oral gavage; twice a day for 2 weeks
Result: Showed dose dependent antitumor activity in SW620 mouse xenograft tumor model.
Molecular Weight

309.30

Formula

C16H12FN5O

CAS No.
SMILES

O=C1N[[email protected]@](C)(C2=NC=NC=C2F)C3=C1C=C(C4=CNN=C4)C=C3

Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : ≥ 30 mg/mL (96.99 mM)

*"≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.2331 mL 16.1655 mL 32.3311 mL
5 mM 0.6466 mL 3.2331 mL 6.4662 mL
10 mM 0.3233 mL 1.6166 mL 3.2331 mL
*Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 2.5 mg/mL (8.08 mM); Clear solution

  • 2.

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (8.08 mM); Clear solution

  • 3.

    Add each solvent one by one:  10% DMSO    90% corn oil

    Solubility: ≥ 2.5 mg/mL (8.08 mM); Clear solution

*All of the co-solvents are available by MCE.
Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
LY3177833
Cat. No.:
HY-100023
Quantity:
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