1. Stem Cell/Wnt JAK/STAT Signaling Immunology/Inflammation Apoptosis
  2. STAT Interleukin Related TNF Receptor
  3. ER-464195-01

ER-464195-01 is an orally active calreticulin (CRT) and integrin α subunits (ITGAs) binding inhibitor. ER-464195-01 inhibits leukocyte infiltration and subsequent inflammatory cascade reactions by dissociating the binding between CRT and ITGA. ER-464195-01 down-regulates the expression of pro-inflammatory genes (such as TNF-α, IL-1β, IL-6, IL-17f) induced by DSS (HY-116282C), and inhibit the phosphorylation of STAT3 and the production of serum amyloid A (SAA). ER-464195-01 can be used for the study of inflammatory bowel disease (IBD).

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

ER-464195-01

ER-464195-01 Chemical Structure

CAS No. : 859218-37-4

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Based on 1 publication(s) in Google Scholar

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Description

ER-464195-01 is an orally active calreticulin (CRT) and integrin α subunits (ITGAs) binding inhibitor. ER-464195-01 inhibits leukocyte infiltration and subsequent inflammatory cascade reactions by dissociating the binding between CRT and ITGA. ER-464195-01 down-regulates the expression of pro-inflammatory genes (such as TNF-α, IL-1β, IL-6, IL-17f) induced by DSS (HY-116282C), and inhibit the phosphorylation of STAT3 and the production of serum amyloid A (SAA). ER-464195-01 can be used for the study of inflammatory bowel disease (IBD)[1].

IC50 & Target[1]

STAT3

 

IL-1β

 

IL-6

 

IL-17F

 

In Vitro

ER-464195-01 (5 μM) effectively inhibits the interaction between CRT and ITGA4 within the Jurkat cells and significantly reduces the level of CRT on the cell surface[1].
ER-464195-01 (0.01-10 μM, 60 min) inhibits the adhesion ability of VCAM-1 cells stimulated by PMA (HY-18739) and ICAM-1 cells stimulated by fMLP (HY-P0224), with IC50 values of 0.15 μM and 0.19 μM respectively, and has no inhibitory effect under MnCl2 stimulation[1].

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

In Vivo

ER-464195-01 (5-10 mg/kg, p.o., once daily for 6-32 days) ameliorates the severity of diseases in IBD mouse models through both prophylactic and therapeutic administration[1].

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

Animal Model: DSS induced IBD model established in female Balb/c mice (9- to 10-week-old)[1]
Dosage: 10 mg/kg (preventive administration) and 5 mg/kg (therapeutic administration)
Administration: Oral administration (p.o.), once daily for 6-7 days
Result: Effectively alleviated the weight loss, increased DAI, and shortened colon in mice under both administration methods.
Reduced the interaction signal between CRT and ITGA4.
Inhibited the upregulation of key pro-inflammatory cytokine mRNAs such as TNF-α, IL1-b, IL-6, and IL-17f induced by DSS.
Inhibited the phosphorylation of STAT3 (p-STAT3) induced by DSS and the production of serum amyloid A (SAA).
Animal Model: CD4+CD45RBhigh T-cell transfer model established in female Balb/c mice (6-week-old)[1]
Dosage: 10 mg/kg
Administration: Oral administration (p.o.), once daily for 32 days
Result: Significantly improved the weight loss in mice and the changes in their fecal characteristics (diarrhea).
Molecular Weight

379.02

Formula

C23H39ClN2

CAS No.
SMILES

CC1(C)CC(C)(C)CC(C2=CC=CC=C2N3CCN(CCC)CC3)C1.Cl

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    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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ER-464195-01
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HY-124686
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