Structure of ATN-161
CAS No.: 262438-43-7
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
ATN-161 is a five-amino-acid peptide derived from the synergy region of fibronectin and a beta integrin antagonist with antitumor activity.
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CAS No. : | 262438-43-7 |
Formula : | C23H35N9O8S |
M.W : | 597.64 |
SMILES Code : | O=C(N)C[C@@H](C(N)=O)NC([C@H](CS)NC([C@H](CO)NC([C@H](CC1=CNC=N1)NC([C@H]2N(C(C)=O)CCC2)=O)=O)=O)=O |
MDL No. : | MFCD30478885 |
InChI Key : | MMHDBUJXLOFTLC-WOYTXXSLSA-N |
Pubchem ID : | 9960285 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
Target |
|
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
Human aortic endothelial cells (HAEC) | 100 μg/mL | 6 hours | Evaluate VCAM-1 and ICAM-1 protein expression | PMC4096780 |
Human aortic endothelial cells (HAEC) | 100 μg/mL | 6 hours | Evaluate oxLDL-induced monocyte adhesion | PMC4096780 |
VeroE6 cells | 1 μM to 10 μM | 1 hour | To assess the ability of ATN-161 to inhibit SARS-CoV-2 infection. Results showed that ATN-161 increased cell viability at concentrations as low as 1 μM and reduced cytopathic effects at 10 μM. | PMC7566794 |
DU145 prostate cancer cells | 1 μg/ml | 24 hours | To evaluate the inhibitory effect of PHSCN peptide on the invasive ability of DU145 cells. Results showed that PHSCN peptide significantly reduced the invasive ability of DU145 cells, with a six-fold decrease compared to untreated cells. | PMC1564117 |
Huh7 cells | 10 μmol/ml | 24 hours | Inhibited OCT4 mRNA expression | PMC9719217 |
HCCLM3 cells | 10 μmol/ml | 24 hours | Inhibited NANOG and OCT4 mRNA expression, reduced YAP activation | PMC9719217 |
Human aortic endothelial cells (HAECs) | 50 μM | 30 minutes | To evaluate the effect of ATN-161 on shear stress-induced endothelial cell activation. Results showed that ATN-161 did not affect shear stress-induced activation of FAK, PAK2, and NF-κB. | PMC4597278 |
HEK293T-ACE2 cells | 0.1 mM | 6 hours | Investigate the effect of ATN-161 on rVSV-S infection, results showed that ATN-161 exhibited no inhibition effect on rVSV-S infection | PMC10723138 |
Adult tenocytes | 100 μM | 60 minutes | To study the effect of ATN-161 on Pro-Hyp uptake, results showed ATN-161 significantly inhibited Pro-Hyp uptake | PMC8239475 |
BEnd.3 cells | 5, 10, 25, and 50 µM | 6h OGD/24h reoxygenation | ATN-161 effectively inhibited OGD/R-induced integrin α5, NLRP3 inflammasome, oxidative stress, mitochondrial damage, fibrosis, and tight junction protein loss. | PMC8380192 |
Human aortic endothelial cells (HAEC) | 100 μg/mL | indicated times | Evaluate VCAM-1 and ICAM-1 mRNA expression | PMC4096780 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Mice | CD4/H11001CD45RBhigh T-cell transfer colitis model | Intraperitoneal injection | 1 mg/kg | Three times a week for six weeks | ATN-161 significantly reduced histopathological scores and angiogenic index in CD4/H11001CD45RBhigh colitis, indicating its therapeutic effect by inhibiting angiogenesis during experimental colitis. | PMC1762465 |
Mice | IL10-deficient mice and DSS-induced colitis model | Intraperitoneal injection | 1 mg/kg | Every other day for 6 weeks | To evaluate the therapeutic effect of ATN-161 on experimental colitis. Results showed that ATN-161 significantly reduced the Disease Activity Index (DAI), histological colitis score, and mean vascular density (MVD), and decreased the production of inflammatory cytokines. | PMC1954843 |
K18-hACE2 transgenic mice | SARS-CoV-2 infection model | Intravenous injection | 1 mg/kg | Single or repeated doses within 48 hours post-infection | Reduced lung viral load, viral immunofluorescence, and improved lung histology | PMC8352850 |
Mice | Ischemic stroke model | Intraperitoneal injection | 1 mg/kg | Immediately after reperfusion, on post-stroke day (PSD)1 and PSD2 | To evaluate the therapeutic effects of ATN-161 on ischemic stroke, results showed ATN-161 significantly reduced infarct volume, edema, and functional deficits, while also reducing BBB permeability and inflammatory responses | PMC7370357 |
BALB/c mice | Colorectal cancer liver metastasis model | Intraperitoneal injection | 1 mg/kg | Every two days | ATN-161 inhibits tumor metastasis | PMC10650826 |
Mice | Stroke model | Intraperitoneal injection | 1 mg/kg | Single dose | To test whether combination treatment of ATN-161 with hNSC transplantation further benefits stroke outcome. Results showed that ATN-161 combined with hNSC transplantation reduced infarct size and attenuated the induction of proinflammatory factors and matrix metalloproteases. | PMC8647207 |
ApoE knockout mice | Atherosclerosis model | Intraperitoneal injection | 5 mg/kg | Three times per week for 7 days | To evaluate the effect of ATN-161 on atherosclerotic plaque formation. Results showed that ATN-161 did not affect plaque formation or inflammatory responses. | PMC4597278 |
ApoE-deficient mice | High-fat Western Diet-induced atherosclerosis model | Intraperitoneal injection | 5 mg/kg | Three times a week for 8 weeks | Evaluate the effect of ATN-161 on atherosclerotic plaque development | PMC4096780 |
Athymic nude mice | DU145 prostate cancer xenograft model | Intravenous injection | 50 mg/kg | Three times per week, continued until the end of the experiment | To evaluate the inhibitory effect of PHSCN peptide on DU145 tumor recurrence and metastasis. Results showed that PHSCN peptide significantly inhibited tumor recurrence and metastasis, with all treated mice remaining recurrence- and metastasis-free for 30 weeks post-surgery. | PMC1564117 |
Clinical Trial:
NCT Number | Conditions | Phases | Recruitment | Completion Date | Locations |
NCT00131651 | Carcinoma, Renal Cell | PHASE2 | TERMINATED | - | University of California Irvin... More >>e, Chao Family Comprehensive Cancer Center, Irvine, California, 92868, United States|University of California San Francisco Comprehensive Cancer Center, San Francisco, California, 94115, United States|The Cleveland Clinic Foundation, Cleveland, Ohio, 44165, United States|University of Wisconsin Comprehensive Cancer Center, Madison, Wisconsin, 53792-6164, United States Less << |
Bio Calculators | ||||
Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.67mL 0.33mL 0.17mL |
8.37mL 1.67mL 0.84mL |
16.73mL 3.35mL 1.67mL |
Tags: ATN-161 | ATN161 | ATN 161 | Integrin | integrin α5β1 antagonist | angiogenesis | tumor growth inhibition | integrin αvβ1 | 262438-43-7
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