964 Results for "

NSC 127669-13C,15N

" in MedChemExpress (MCE) Product Catalog:
Products (964)

964 Results for "NSC 127669-13C,15N" in MCE Product Catalog:

24
24 Cited Publications
Cat. No.: HY-15037
CAS No.: 15307-79-6
Purity:  99.94%
Synonyms: GP 45840
Target:  

COX Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

Diclofenac Sodium (GP 45840) is a potent and nonselective anti-inflammatory agent, acts as a COX inhibitor, with IC50s of 4 and 1.3 nM for human COX-1 and COX-2 in CHO cells , and 5.1 and 0.84 μM for ovine COX-1 and COX-2, respectively . Diclofenac Sodium induces apoptosis of neural stem cells (NSCs) via the activation of the caspase cascade .
24
24 Cited Publications
Cat. No.: HY-N1150
CAS No.: 50-89-5
Synonyms: DThyd; NSC 21548
Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication .
22
22 Cited Publications
Cat. No.: HY-18980
CAS No.: 82-08-6
Synonyms: Mallotoxin; NSC 56346; NSC 94525
Rottlerin, a natural product purified from Mallotus Philippinensis, is a specific PKC inhibitor, with IC50 values for PKCδ of 3-6 μM, PKCα,β,γ of 30-42 μM, PKCε,η,ζ of 80-100 μM. Rottlerin acts as a direct mitochondrial uncoupler, and stimulates autophagy by targeting a signaling cascade upstream of mTORC1. Rottlerin induces apoptosis via caspase 3 activation . Rottlerin inhibits HIV-1 integration and Rabies virus (RABV) infection .
22
22 Cited Publications
Cat. No.: HY-15457
CAS No.: 35943-35-2
Purity:  98.62%
Synonyms: API-2; NSC 154020; TCN
Target:  

DNA/RNA Synthesis Akt HIV

Research Areas:  

Cancer

Triciribine is a DNA synthesis inhibitor, also inhibits Akt and HIV-1/2 with IC50 of 130 nM, and 0.02-0.46 μM, respectively.
22
22 Cited Publications
Cat. No.: HY-12519
CAS No.: 64224-21-1
Purity:  99.87%
Synonyms: RP 35972; NSC 347901
Research Areas:  

Cancer

Oltipraz has an inhibitory effect on HIF-1α activation in a time-dependent manner, completely abrogating HIF-1α induction at ≥10 μM concentrations, the IC50 of Oltipraz for HIF-1α inhibition is 10 μM. Oltipraz is a potent Nrf2 activator.
20
20 Cited Publications
Cat. No.: HY-101084
CAS No.: 113104-25-9
Purity:  ≥98.0%
NSC 228155 is an activator of EGFR, binds to the extracellular region of EGFR and enhance tyrosine phosphorylation of EGFR . NSC 228155 is also a potent inhibitor of KIX-KID interaction, inhibits kinase-inducible domain (KID) from CREB and KID-interacting domain (KIX) from CBP, with an IC50 of 0.36 μM .
20
20 Cited Publications
Cat. No.: HY-101838
CAS No.: 1799711-21-9
Purity:  98.96%
Research Areas:  

Cancer

dBET1 is a PROTAC connected by ligands for Cereblon and BRD4 with an EC50 of 430 nM. dBET1 is a PROTAC that composes of (+)-JQ1 (HY-13030) linked to NSC 527179 (HY-14658) with a linker .
19
19 Cited Publications
Cat. No.: HY-50909
CAS No.: 157716-52-4
Synonyms: KRX-0401; NSC 639966; D21266
Target:  

Akt Autophagy Apoptosis

Research Areas:  

Cancer

Perifosine is an oral Akt inhibitor which inhibits proliferation of different tumor cell lines with IC50s of 0.6-8.9 μM.
19
19 Cited Publications
Cat. No.: HY-76201
CAS No.: 149003-01-0
Synonyms: ICRF-187 hydrochloride; ADR-529 hydrochloride; NSC-169780 hydrochloride
Dexrazoxane hydrochloride (ICRF-187 hydrochloride) is a heart protectant that can help preserve ovarian function and fertility. Dexrazoxane hydrochloride has antioxidant and anti-inflammatory properties, can cross the blood-brain barrier, improves motor function disorders, and offers neuroprotective effects, making it useful in the study of neurodegenerative diseases .
19
19 Cited Publications
Cat. No.: HY-B0581
CAS No.: 24584-09-6
Synonyms: ICRF-187; ADR-529; NSC-169780
Dexrazoxane, as an intracellular iron chelating agent, reduces the formation of superoxide radicals and has cardioprotective, anti-inflammatory, antioxidant, anti-tumor and neuroprotective activities. Dexrazoxane inhibits ferroptosis of H9c2 cells by inhibiting HMGB1. Dexrazoxane induces DNA damage and apoptosis in human fibrosarcoma cells .
17
17 Cited Publications
Cat. No.: HY-13764
CAS No.: 518-34-3
Purity:  99.90%
Synonyms: NSC-77037; d-Tetrandrine
Tetrandrine (NSC-77037; d-Tetrandrine) is a bis-benzyl-isoquinoline alkaloid, which inhibits voltage-gated Ca 2+ current (ICa) and Ca 2+-activated K + current.
17
17 Cited Publications
Cat. No.: HY-B0246
CAS No.: 298-46-4
Synonyms: CBZ; NSC 169864
Carbamazepine is an orally active pressure-sensitive sodium ion channel blocker with an IC50 of 131 μM. Carbamazepine blocks voltage gated Na +, Ca 2+, and K + channels, and is also a HDAC inhibitor (IC50: 2 μM). Carbamazepine is an anticonvulsant and can be used for research of epilepsy and neuropathic pain .
16
16 Cited Publications
Cat. No.: HY-N0054
CAS No.: 484-12-8
Synonyms: Osthol; NSC 31868
Osthole (Osthol) is a natural antihistamine alternative. Osthole may be a potential inhibitor of histamine H1 receptor activity. Osthole also suppresses the secretion of HBV in cells.
16
16 Cited Publications
Cat. No.: HY-10389
CAS No.: 467214-20-6
Purity:  99.59%
Synonyms: 17-DMAG; KOS-1022; NSC 707545
Target:  

HSP

Research Areas:  

Cancer

Alvespimycin (17-DMAG) is a potent inhibitor of Hsp90, binding to Hsp90 with an EC50 of 62 nM.
15
15 Cited Publications
Cat. No.: HY-N0133
CAS No.: 481-53-8
Synonyms: Tangeritin; NSC53909; NSC618905
Tangeretin (Tangeritin), a flavonoid from citrus fruit peels, has been proven to play an important role in anti-inflammatory responses and neuroprotective effects in several disease models, and is a Notch-1 inhibitor.
15
15 Cited Publications
Cat. No.: HY-B0217
CAS No.: 55981-09-4
Synonyms: NTZ; NSC 697855
Research Areas:  

Infection Cancer

Nitazoxanide (NTZ), an anthelmintic agent, exhibits a broad spectrum of activities against a wide variety of helminths, protozoa, and enteric bacteria infecting animals and humans. Nitazoxanide inhibits Giardia lamblia trophozoite proliferation in axenic culture with an IC50 of 2.4 μM . Nitazoxanide can be used for the research of parasitic gastroenteritis. Nitazoxanide shows anti-Japanese encephalitis virus (JEV) activity in a mouse model .
15
15 Cited Publications
Cat. No.: HY-14394
CAS No.: 17374-26-4
Purity:  98.54%
Synonyms: NSC 231634; Casein Kinase II Inhibitor I
Target:  

Casein Kinase

Research Areas:  

Cancer

TBB is a cell-permeable and ATP-competitive CK2 inhibitor with an IC50 of 0.15 μM for rat liver CK2.
15
15 Cited Publications
Cat. No.: HY-12302
CAS No.: 142273-20-9
Purity:  98.20%
Synonyms: 9-Bromopaullone; NSC-664704
Target:  

CDK GSK-3

Research Areas:  

Cancer

Kenpaullone is a potent inhibitor of CDK1/cyclin B and GSK-3β, with IC50s of 0.4 μM and 23 nM, and also inhibits CDK2/cyclin A, CDK2/cyclin E, and CDK5/p25 with IC50s of 0.68 μM, 7.5 μM, 0.85 μM, respectively. Kenpaullone, a small molecule inhibitor of KLF4, reduces self-renewal of breast cancer stem cells and cell motility in vitro.
14
14 Cited Publications
Cat. No.: HY-10475
CAS No.: 102121-60-8
Purity:  98.38%
Synonyms: CD336; NSC608001; Ro 40-6055
Target:  

RAR/RXR Autophagy

Research Areas:  

Cancer

AM580 is a selective RARα agonist with IC50 and EC50 of 8 nM and 0.36 nM, respectively.
13
13 Cited Publications
Cat. No.: HY-19387
CAS No.: 69839-83-4
Synonyms: NSC-324360
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Didox (NSC-324360) is a synthetic ribonucleotide reductase (RR) inhibitor.