1060 Results for "

Novel

" in MedChemExpress (MCE) Product Catalog:
Products (1060)

1060 Results for "Novel" in MCE Product Catalog:

138
138 Publications Verification
Cat. No.: HY-B0075
CAS No.: 73-31-4
Synonyms: N-Acetyl-5-methoxytryptamine
Melatonin is a hormone made by the pineal gland that can activate melatonin receptor and inhibit PANoptosis. Melatonin plays a role in sleep and possesses important antioxidative and anti-inflammatory properties . Melatonin is a novel selective ATF-6 inhibitor and induces human hepatoma cell apoptosis through COX-2 downregulation . Melatonin attenuates palmitic acid-induced (HY-N0830) mouse granulosa cells apoptosis via endoplasmic reticulum stress .
138
138 Publications Verification
Cat. No.: HY-B0075R
CAS No.: 73-31-4
Synonyms: N-Acetyl-5-methoxytryptamine (standard); Melatonin
Melatonin (Standard) is the analytical standard of Melatonin. This product is intended for research and analytical applications. Melatonin is a hormone made by the pineal gland that can activates melatonin receptor. Melatonin plays a role in sleep and possesses important antioxidative and anti-inflammatory properties . Melatonin is a novel selective ATF-6 inhibitor and induces human hepatoma cell apoptosis through COX-2 downregulation . Melatonin attenuates palmitic acid-induced (HY-N0830) mouse granulosa cells apoptosis via endoplasmic reticulum stress .
104
104 Cited Publications
Cat. No.: HY-108413
CAS No.: 1373431-65-2
Purity:  99.95%
Synonyms: BMN 673ts
Target:  

PARP

Research Areas:  

Cancer

Talazoparib tosylate (BMN 673ts) is a novel, potent and orally available PARP1/2 inhibitor with an IC50 of 0.57 nM for PARP1.
63
63 Cited Publications
Cat. No.: HY-13064A
CAS No.: 1369665-02-0
Purity:  99.73%
Synonyms: GDC-0973 hemifumarate; XL-518 hemifumarate
Target:  

MEK Apoptosis

Research Areas:  

Cancer

Cobimetinib hemifumarate is a novel selective MEK1 inhibitor, and the IC50 value against MEK1 is 4.2 nM.
59
59 Cited Publications
Cat. No.: HY-13671
CAS No.: 934593-90-5
Purity:  98.47%
Synonyms: HIF-1α inhibitor; LW8
Research Areas:  

Cancer

LW6 (HIF-1α inhibitor) is a novel HIF-1 inhibitor with an IC50 value of 4.4 μM, and it is also an inhibitor of MDH2. LW6 decreases HIF-1α protein expression without affecting HIF-1β expression.
58
58 Cited Publications
Cat. No.: HY-12289
CAS No.: 1073154-85-4
Purity:  99.87%
Synonyms: VS-6063; PF-04554878
Target:  

FAK

Research Areas:  

Cancer

Defactinib (VS-6063; PF-04554878) is a novel FAK inhibitor with potential antiangiogenic and antineoplastic activities.
58
58 Cited Publications
Cat. No.: HY-12289A
CAS No.: 1073160-26-5
Purity:  99.35%
Synonyms: VS-6063 hydrochloride; PF 04554878 hydrochloride
Target:  

FAK

Research Areas:  

Cancer

Defactinib hydrochloride (VS-6063 hydrochloride; PF 04554878 hydrochloride) is a novel FAK inhibitor, which inhibits FAK phosphorylation at the Tyr397 site in a time- and dose-dependent manner.
44
44 Cited Publications
Cat. No.: HY-B0099
CAS No.: 89-25-8
Synonyms: MCI-186
Target:  

MMP Apoptosis

Research Areas:  

Neurological Disease

Edaravone is a strong novel free radical scavenger, and inhibits MMP-9-related brain hemorrhage in rats treated with tissue plasminogen activator.
41
41 Cited Publications
Cat. No.: HY-125033
CAS No.: 3258-02-4
Purity:  99.96%
Synonyms: β-D-N4-hydroxycytidine; NHC
Research Areas:  

Infection

EIDD-1931 (Beta-d-N4-hydroxycytidine; NHC) is a novel nucleoside analog and behaves as a potent anti-virus agent. EIDD-1931 effectively inhibits the replication activity of venezuelan equine encephalitis virus (VEEV), Chikungunya virus (CHIKV) and hepatitis C virus (HCV) .
40
40 Cited Publications
Cat. No.: HY-10820B
CAS No.: 357166-29-1
Purity:  99.46%
Synonyms: LY231514 disodium heptahydrate
Target:  

Antifolate Autophagy

Research Areas:  

Cancer

Pemetrexed disodium heptahydrate is a novel antifolate, the Ki values of the pentaglutamate of LY231514 are 1.3, 7.2, and 65 nM for inhibits thymidylate synthase (TS), dihydrofolate reductase (DHFR), and glycinamide ribonucleotide formyltransferase (GARFT), respectively.
26
26 Cited Publications
Cat. No.: HY-15192
CAS No.: 890842-28-1
Purity:  99.76%
Target:  

SGK Influenza Virus

Research Areas:  

Infection Cancer

GSK 650394 is a novel SGK inhibitor with IC50 of 62 nM and 103 nM for SGK1 and SGK2 in the SPA assay respectively. GSK 650394 also inhibits influenza virus replication.
25
25 Cited Publications
Cat. No.: HY-12009
CAS No.: 635702-64-6
Purity:  99.99%
Synonyms: GW786034 Hydrochloride
Research Areas:  

Cancer

Pazopanib Hydrochloride (GW786034 Hydrochloride) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with an IC50 of 10, 30, 47, 84, 74, 140 and 146 nM, respectively.
25
25 Cited Publications
Cat. No.: HY-10208
CAS No.: 444731-52-6
Purity:  99.91%
Synonyms: GW786034
Research Areas:  

Cancer

Pazopanib (GW786034) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ, c-Kit, FGFR1, and c-Fms with IC50s of 10, 30, 47, 84, 74, 140 and 146 nM, respectively.
20
20 Cited Publications
Cat. No.: HY-16665
CAS No.: 677331-12-3
Target:  

Wnt

Research Areas:  

Cancer

iCRT 14 is a novel potent inhibitor of β-catenin-responsive transcription (CRT), with IC50 of 40.3 nM against Wnt responsive STF16 luciferase.
20
20 Cited Publications
Cat. No.: HY-18360
CAS No.: 1314890-29-3
Target:  

HDAC

Research Areas:  

Cancer

TMP269 is a novel and selective class IIa histone deacetylase (HDAC) inhibitor with IC50s of 157 nM, 97 nM, 43 nM and 23 nM for HDAC4, HDAC5, HDAC7 and HDAC9, respectively.
19
19 Cited Publications
Cat. No.: HY-14855
CAS No.: 856866-72-3
Purity:  99.03%
Synonyms: TR 700; Torezolid; DA-7157
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Tedizolid (TR 700; Torezolid; DA-7157) is a novel oxazolidinone, acting through inhibition of bacterial protein synthesis by binding to 23S ribosomal RNA (rRNA) of the 50S subunit of the ribosome.
19
19 Cited Publications
Cat. No.: HY-15515
CAS No.: 223104-29-8
Purity:  99.95%
Target:  

Na+/Ca2+ Exchanger

Research Areas:  

Cardiovascular Disease

SEA0400 is a novel and selective inhibitor of the Na +-Ca 2+ exchanger (NCX), inhibiting Na +-dependent Ca 2+ uptake in cultured neurons, astrocytes, and microglia with IC50s of from 5 to 33 nM.
17
17 Cited Publications
Cat. No.: HY-119706
CAS No.: 356568-70-2
Purity:  98.93%
Target:  

Apoptosis Arrestin

Research Areas:  

Others

Barbadin is a novel and selective β-arrestin/β2-adaptin interaction inhibitor, has IC50 values of 19.1 μM for β-arrestin1 and 15.6 μM for β-arrestin2. Barbadin blocks agonist-promoted endocytosis of the prototypical β2-adrenergic, V2-vasopressin and angiotensin-II type-1 receptors. Barbadin can induce apoptosis .
16
16 Cited Publications
Cat. No.: HY-14711
CAS No.: 656820-32-5
Purity:  99.22%
Target:  

Aurora Kinase Autophagy

Research Areas:  

Cancer

Reversine is a novel class of ATP-competitive Aurora kinase inhibitor with IC50s of 400, 500 and 400 nM for Aurora A, Aurora B and Aurora C, respectively.
16
16 Cited Publications
Cat. No.: HY-N0060
CAS No.: 1135-24-6
Synonyms: Coniferic acid
Ferulic acid is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC50s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively.