Structure of NG 52
CAS No.: 212779-48-1
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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.
NG 52 is a potent, cell-permeable, reversible, selective, and ATP-compatible inhibitor of the cell cycle-regulating kinase, Cdc28p (IC50 = 7 μM), and the related Pho85p kinase (IC50 = 2 μM).
Synonyms: Compound 52
4.5
*For Research Use Only !
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Batch number can be found on the product's label following the word 'Batch'.
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.
Batch number can be found on the product's label following the word 'Batch'.
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.
Batch number can be found on the product's label following the word 'Batch'.
CAS No. : | 212779-48-1 |
Formula : | C16H19ClN6O |
M.W : | 346.81 |
SMILES Code : | CC(N1C=NC2=C(NC3=CC=CC(Cl)=C3)N=C(NCCO)N=C12)C |
Synonyms : |
Compound 52
|
MDL No. : | MFCD02179196 |
InChI Key : | XZEFMZCNXDQXOZ-UHFFFAOYSA-N |
Pubchem ID : | 2856 |
GHS Pictogram: |
![]() |
Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
MDA-MB-468 | 7 ng/mL | 72 hours | Evaluate cytotoxicity of 806-PE38 on MDA-MB-468 cells, IC50 was 7 ng/mL | PMC5017938 |
HCC70 | 4 ng/mL | 72 hours | Evaluate cytotoxicity of 806-PE38 on HCC70 cells, IC50 was 4 ng/mL | PMC5017938 |
BT-20 | 10 ng/mL | 72 hours | Evaluate cytotoxicity of 806-PE38 on BT-20 cells, IC50 was 10 ng/mL | PMC5017938 |
HiPSC-derived neurons | 20 μM | Evaluate the inhibitory effect of adamantane series inhibitors in cells | PMC7478247 | |
Neuro-2a | 30 μM | Evaluate the inhibitory effect of Fmoc-D-Cys(trt)-OH on BoNT/A LC | PMC7478247 | |
WI-38 | >300 ng/mL | 72 hours | Evaluate cytotoxicity of 806-PE38 on WI-38 cells, IC50>300 ng/mL | PMC5017938 |
HCC1937 | 90 ng/mL | 72 hours | Evaluate cytotoxicity of 806-PE38 on HCC1937 cells, IC50 was 90 ng/mL | PMC5017938 |
HCC1395 | 30 ng/mL | 72 hours | Evaluate cytotoxicity of 806-PE38 on HCC1395 cells, IC50 was 30 ng/mL | PMC5017938 |
MDA-MB-231 | 90 ng/mL | 72 hours | Evaluate the toxicity of HTCG@TA on MDA-MB-231 cells, results showed only 32% cell survival | PMC5017938 |
HER2-A775_G776YVMA-inserted lung adenocarcinoma patient-derived organoids | 180 nM | 72 hours | Evaluate the growth inhibitory effect of pyrotinib on HER2-mutant lung cancer cells, results showed pyrotinib at plasma concentration significantly inhibited cell growth more than afatinib | PMC7360147 |
THP-1 macrophages | 5 μg/cm2 | 24 hours | To evaluate the intracellular antibacterial activity of levofloxacin in THP-1 macrophages. Results showed that 20(S)-Rh2 significantly enhanced the bactericidal effect of levofloxacin against intracellular S. aureus in a concentration- and time-dependent manner. | PMC7776606 |
Primary human mesothelial cells | 5 μg/cm2 | 24 hours | Assessed DNA damage repair, showing delayed H2A.X phosphorylation in BLM-silenced cells | PMC7776606 |
Murine mesothelial cells | 5 μg/cm2 | 8 hours | Assessed genomic instability, showing significantly increased micronuclei frequency in Blm+/− cells | PMC7776606 |
Mouse cortical neurons | 30 ng/ml | 2 hours | To evaluate the neuroprotective effects of leptin against NMDA-induced toxicity, results showed that leptin was protective in Slo1+/+ neurons but ineffective in Slo1+/− and Slo1−/− neurons | PMC4134969 |
Rat cortical neurons | 10–100 ng/ml | 2 hours | To evaluate the neuroprotective effects of leptin against NMDA-induced toxicity, results showed that leptin significantly reduced NMDA-induced cell death when preincubated for 2 hours | PMC4134969 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Female athymic nude mice | MDA-MB-468 or HCC70 xenograft model | Tail vein injection | 5 μg/mouse | Every other day for four times | Evaluate the antitumor efficacy of 806-PE38 in MDA-MB-468 and HCC70 xenograft models, results showed that 806-PE38 significantly reduced tumor burden and prolonged survival time | PMC5017938 |
BALB/c nude mice | HER2-A775_G776YVMA-inserted lung adenocarcinoma patient-derived xenograft model | Oral | 5 mg/kg, 20 mg/kg, 80 mg/kg | Once daily for 24 days | Evaluate the antitumor effect of pyrotinib in vivo, results showed 80 mg/kg pyrotinib significantly reduced tumor volume (mean reduction of 52.2%) and was superior to afatinib and T-DM1 | PMC7360147 |
Mouse | Lethality assay | Intraperitoneal injection | 1 mg/kg | Single dose | Evaluate the protective effect of copper-ligand complexes on BoNT/A intoxicated mice | PMC7478247 |
Mice | Genetically engineered mouse models (GEMM) of small-cell lung cancer (SCLC), pancreatic ductal adenocarcinoma (PDAC), and non-small cell lung cancer (NSCLC) | Blood exchange | Several hours | To measure the kinetics of endogenous CTCs, including their half-life in circulation and generation rate, and to assess the metastatic propensity of CTCs. Results showed that the half-life of CTCs ranged between 40 and 260 seconds, and the generation rate varied between 60 and 107,000 CTCs/hour. Additionally, direct transfer of 1-2% of CTCs generated macrometastases in healthy recipient mice. | PMC8479082 | |
Mice | Blm+/− mice | Intraperitoneal injection | 5 mg | Twice a week for 5 weeks | Assessed inflammatory response and mesothelioma incidence, showing Blm+/? mice had enhanced inflammation and significantly higher mesothelioma incidence | PMC7776606 |
Bio Calculators | ||||
Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.88mL 0.58mL 0.29mL |
14.42mL 2.88mL 1.44mL |
28.83mL 5.77mL 2.88mL |
Tags: NG 52 | Compound 52 | NG52 | NG-52 | Compound52 | Compound-52 | CDK | Cyclin dependent kinase | CDK2 | Cdc28p | Pho85p | ATP-compatible | cdc2-cyclin B | yeast | PGK1 | anti-proliferation | PDHK1 | Warburg | 212779-48-1
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P301 + P312 | IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell. |
P301 + P330 + P331 | IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. |
P302 + P334 | IF ON SKIN: Immerse in cool water/wrap in wet bandages. |
P302 + P350 | IF ON SKIN: Gently wash with plenty of soap and water. |
P303 + P361 + P353 | IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower. |
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P304 + P340 | IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing. |
P304 + P341 | IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. |
P305 + P351 + P338 | IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. |
P306 + P360 | IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes. |
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P308 + P313 | IF exposed or concerned: Get medical advice/attention. |
P309 + P311 | IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician. |
P332 + P313 | IF SKIN irritation occurs: Get medical advice/attention. |
P333 + P313 | IF SKIN irritation or rash occurs: Get medical advice/attention. |
P335 + P334 | Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages. |
P337 + P313 | IF eye irritation persists: Get medical advice/attention. |
P342 + P311 | IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician. |
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H201 | Explosive; mass explosion hazard |
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H231 | May react explosively even in the absence of air at elevated pressure and/or temperature |
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H242 | Heating may cause a fire |
H250 | Catches fire spontaneously if exposed to air |
H251 | Self-heating; may catch fire |
H252 | Self-heating in large quantities; may catch fire |
H260 | In contact with water releases flammable gases which may ignite spontaneously |
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Health hazards | |
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H303 | May be harmful if swallowed |
H304 | May be fatal if swallowed and enters airways |
H305 | May be harmful if swallowed and enters airways |
H310 | Fatal in contact with skin |
H311 | Toxic in contact with skin |
H312 | Harmful in contact with skin |
H313 | May be harmful in contact with skin |
H314 | Causes severe skin burns and eye damage |
H315 | Causes skin irritation |
H316 | Causes mild skin irritation |
H317 | May cause an allergic skin reaction |
H318 | Causes serious eye damage |
H319 | Causes serious eye irritation |
H320 | Causes eye irritation |
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H331 | Toxic if inhaled |
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H333 | May be harmful if inhaled |
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H336 | May cause drowsiness or dizziness |
H340 | May cause genetic defects |
H341 | Suspected of causing genetic defects |
H350 | May cause cancer |
H351 | Suspected of causing cancer |
H360 | May damage fertility or the unborn child |
H361 | Suspected of damaging fertility or the unborn child |
H361d | Suspected of damaging the unborn child |
H362 | May cause harm to breast-fed children |
H370 | Causes damage to organs |
H371 | May cause damage to organs |
H372 | Causes damage to organs through prolonged or repeated exposure |
H373 | May cause damage to organs through prolonged or repeated exposure |
Environmental hazards | |
Code | Phrase |
H400 | Very toxic to aquatic life |
H401 | Toxic to aquatic life |
H402 | Harmful to aquatic life |
H410 | Very toxic to aquatic life with long-lasting effects |
H411 | Toxic to aquatic life with long-lasting effects |
H412 | Harmful to aquatic life with long-lasting effects |
H413 | May cause long-lasting harmful effects to aquatic life |
H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
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