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Chemical Structure| 1416324-85-0 Chemical Structure| 1416324-85-0

Structure of CU-CPT22
CAS No.: 1416324-85-0

Chemical Structure| 1416324-85-0

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Selective toll-like receptor 1/2 (TLR1/2) inhibitor (IC50 = 0.58 μM). Exhibits no activity at TLR2/TLR6, TLR3, TLR4 and TLR7 or a panel of 10 representative kinases. Inhibits the release of proinflammatory cytokines TNF-α and IL-1β.

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Product Details of CU-CPT22

CAS No. :1416324-85-0
Formula : C19H22O7
M.W : 362.37
SMILES Code : O=C(C(C=C1O)=CC2=CC(OC)=C(O)C(O)=C2C1=O)OCCCCCC
MDL No. :MFCD26406409
InChI Key :UBQFTTUFRSSOHE-UHFFFAOYSA-N
Pubchem ID :71503400

Safety of CU-CPT22

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H334-H410
Precautionary Statements:P261-P273-P342+P311-P501
Class:9
UN#:3077
Packing Group:

Related Pathways of CU-CPT22

pyroptosis
TLR

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Primary mouse microglia 10 µM 2 hours To investigate the effect of CU-CPT22 on SynO-induced NF-κB nuclear translocation, results showed that CU-CPT22 significantly reduced NF-κB nuclear translocation. Sci Signal. 2015 May 12;8(376):ra45.
RAW 264.7 macrophage cells 0.58 ± 0.09 µM Inhibits TLR1/2 signaling, reduces NO production Angew Chem Int Ed Engl. 2012 Dec 3;51(49):12246-9.
HEK293-hTLR2 cells 1, 5, 10, 20 µM 16 hours CU-CPT22 inhibited Pam3CSK4-induced TLR2/1 heterodimerization Nutrients. 2018 Jul 5;10(7):868.
Raw264.7 cells 10 µM and 20 µM 16 hours CU-CPT22 significantly inhibited Pam3CSK4-induced TRL2/1 signaling Nutrients. 2018 Jul 5;10(7):868.

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6 mice MPTP-induced Parkinson's disease model Injection 3 mg/kg Once daily for 35 days To investigate the protective effect of CU-CPT22 on MPTP-induced autonomic dysfunction, results showed that CU-CPT22 improved gastrointestinal symptoms, urinary frequency, and cardiovascular function Cell Death Discov. 2024 Jan 26;10(1):52.
C57BL/6J mice MPTP-induced Parkinson’s disease model Intraperitoneal injection 3 mg/kg Administered 30 min prior to MPTP injection, lasted for 5 weeks CU-CPT22, as a TLR2 antagonist, ameliorated MPTP-induced motor dysfunction and nerve conduction damage, reduced p-α-syn accumulation and TLR2/NF-κB pathway activation Cell Death Discov. 2021 Oct 12;7(1):289
CD-1 male mice Cecal ligation and puncture (CLP) model Intraperitoneal injection 3 mg/kg/day 2 days CU-CPT22 attenuated sepsis-induced neuroinflammation and cognitive dysfunction J Mol Med (Berl). 2018 May;96(5):391-402

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.76mL

0.55mL

0.28mL

13.80mL

2.76mL

1.38mL

27.60mL

5.52mL

2.76mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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