Structure of NCB-0846
CAS No.: 1792999-26-8
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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.
NCB-0846 is an TNIK inhibitor with IC50 value of 21 nM.
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Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
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CAS No. : | 1792999-26-8 |
Formula : | C21H21N5O2 |
M.W : | 375.42 |
SMILES Code : | O[C@H]1CC[C@@H](OC2=CC=CC3=CN=C(NC4=CC=C5C(NC=N5)=C4)N=C23)CC1 |
MDL No. : | MFCD30749187 |
InChI Key : | FYWRWBSYRGSWIQ-UHFFFAOYSA-N |
Pubchem ID : | 91801204 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
HEK293 | 0.1-0.3 µM | 24 hours | Inhibition of TCF/LEF transcriptional activity | Nat Commun. 2016 Aug 26;7:12586 |
DLD-1 | 0.1-0.3 µM | 24 hours | Inhibition of TCF/LEF transcriptional activity | Nat Commun. 2016 Aug 26;7:12586 |
HCT116 | 0.1-0.3 µM | 24 hours | Inhibition of TCF/LEF transcriptional activity | Nat Commun. 2016 Aug 26;7:12586 |
PDX cells | 0–10 µM | 12 days | To assess the effect of NCB-0846 on colony formation, results showed that NCB-0846 significantly reduced colony formation. | Neoplasia. 2019 Apr;21(4):389-400 |
PDX cells | 0–10 µM | 1-5 days | To assess the effect of NCB-0846 on cell viability, results showed that NCB-0846 significantly reduced cell viability. | Neoplasia. 2019 Apr;21(4):389-400 |
PDX cells | 0–10 µM | 24 hours | To assess the effect of NCB-0846 on TNIK and TNIK (pS764) expression, results showed that NCB-0846 significantly decreased TNIK and TNIK (pS764) levels. | Neoplasia. 2019 Apr;21(4):389-400 |
MC3T3-E1 osteoblasts | 0.2 µM | 24 hours | To study the effect of NCB-0846 on collagen deposition in osteoblasts. Results showed that NCB-0846 treatment did not limit collagen deposition. | Hepatol Commun. 2022 Mar;6(3):593-609 |
Primary human hepatic stellate cells | 0.1 µM | 24 hours | To evaluate the inhibition of TNIK kinase activity by NCB-0846 and its effect on procollagen I secretion. It was found that NCB-0846 treatment reduced secretion of collagen I and fibronectin without affecting procollagen I transcription. | Hepatol Commun. 2022 Mar;6(3):593-609 |
LX-2 cells | 0.1 µM | 24 hours | To investigate the inhibitory effect of NCB-0846 on TNIK kinase activity and its impact on procollagen I secretion. Results showed that NCB-0846 treatment limited TNIK autophosphorylation and reduced secretion of collagen I and fibronectin. | Hepatol Commun. 2022 Mar;6(3):593-609 |
PDX cells | 0–10 µM | 4 weeks | To assess the effect of NCB-0846 on anchorage-independent growth in soft agar, results showed that NCB-0846 significantly reduced colony number and size. | Neoplasia. 2019 Apr;21(4):389-400 |
LUDLU1 | 300 nM | 48 hours | To evaluate the radiosensitizing effect of NCB-0846 on TNIKlow LSCC cells, results showed that NCB-0846 did not significantly reduce the survival of TNIKlow cells. | Mol Cancer Ther. 2024 Apr 27;23(8):1201–11 |
KNS62 | 300 nM | 48 hours | To evaluate the radiosensitizing effect of NCB-0846 on TNIKlow LSCC cells, results showed that NCB-0846 did not significantly reduce the survival of TNIKlow cells. | Mol Cancer Ther. 2024 Apr 27;23(8):1201–11 |
SW900 | 300 nM | 48 hours | To evaluate the radiosensitizing effect of NCB-0846 on TNIKhigh LSCC cells, results showed that pretreatment with NCB-0846 significantly reduced the survival of TNIKhigh cells. | Mol Cancer Ther. 2024 Apr 27;23(8):1201–11 |
H520 | 300 nM | 48 hours | To evaluate the radiosensitizing effect of NCB-0846 on TNIKhigh LSCC cells, results showed that pretreatment with NCB-0846 significantly reduced the survival of TNIKhigh cells. | Mol Cancer Ther. 2024 Apr 27;23(8):1201–11 |
LK2 | 300 nM | 48 hours | To evaluate the radiosensitizing effect of NCB-0846 on TNIKhigh LSCC cells, results showed that pretreatment with NCB-0846 significantly reduced the survival of TNIKhigh cells. | Mol Cancer Ther. 2024 Apr 27;23(8):1201–11 |
NCI-H2228 cells | 1 µM | 48 hours | NCB-0846 modestly inhibited TGF β1-induced EMT in H2228 cells, but the effect on EMT markers was not obvious. | Br J Cancer. 2021 Jan;124(1):228-236 |
A549 cells | 1 µM | 48 hours | NCB-0846 inhibited TGF β1-induced EMT in A549 cells, restored E-cadherin expression, and suppressed mesenchymal markers vimentin and N-cadherin. | Br J Cancer. 2021 Jan;124(1):228-236 |
Aska | >2.0 µM | 72 hours | Evaluate the inhibitory effect of NCB-0846 on Aska cells, results showed IC50 exceeding 2.0 µM, cells were insensitive to the drug | Cancers (Basel). 2020 May 16;12(5):1258 |
Yamato | 767 nM | 72 hours | Evaluate the inhibitory effect of NCB-0846 on Yamato cells, results showed IC50 of 767 nM, significantly inhibiting cell viability | Cancers (Basel). 2020 May 16;12(5):1258 |
SYO-1 | 356 nM | 72 hours | Evaluate the inhibitory effect of NCB-0846 on SYO-1 cells, results showed IC50 of 356 nM, significantly inhibiting cell viability | Cancers (Basel). 2020 May 16;12(5):1258 |
HS-SY-II | 339 nM | 72 hours | Evaluate the inhibitory effect of NCB-0846 on HS-SY-II cells, results showed IC50 of 339 nM, significantly inhibiting cell viability | Cancers (Basel). 2020 May 16;12(5):1258 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
C57BL/6J mice | CCl4-induced liver fibrosis model | Intraperitoneal injection | 10 mg/kg | 5 times per week for 4 weeks | To evaluate the inhibitory effect of NCB-0846 on liver fibrosis in vivo. Results showed that NCB-0846 treatment reduced CCl4-induced fibrosis and decreased expression of collagen I and fibronectin. | Hepatol Commun. 2022 Mar;6(3):593-609 |
NOD-scid IL2Rgammanull mice | Subcutaneous xenograft model | Oral gavage | 100 mg/kg | Administered on days 1, 3, and 5, lasting for 1 week | To evaluate the radiosensitizing effect of NCB-0846 on TNIKhigh LSCC tumors, results showed that pretreatment with NCB-0846 significantly enhanced the efficacy of IR and caused elevated necrosis in TNIKhigh LK2 tumors but not TNIKlow KNS62 tumors. | Mol Cancer Ther. 2024 Apr 27;23(8):1201–11 |
Mice | Apcmin/þ mice | Oral | 22.5-90 mg/kg | BID for 35 days | Suppression of Wnt-driven intestinal tumorigenesis | Nat Commun. 2016 Aug 26;7:12586 |
SCID mice | A549 cell lung metastasis model | Tail vein injection | 3 µM | Single injection, observed for 7 weeks | NCB-0846 significantly reduced the metastatic lesion area in the lungs of SCID mice injected with TGF β1-treated A549 cells. | Br J Cancer. 2021 Jan;124(1):228-236 |
NOD/SCID mice | Subcutaneous xenograft model | Oral | 80 mg/kg | Twice daily for 5 days | Evaluate the inhibitory effect of NCB-0846 on subcutaneous xenografts, results showed significant reduction in tumor volume | Cancers (Basel). 2020 May 16;12(5):1258 |
Tags: NCB-0846 | NCB0846 | NCB 0846 | Wnt signalling pathway | MAP4K | MAPK Kinase Kinase Kinase | inhibitor | 1792999-26-8 |
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