16 Results for "

METTL3-IN-14

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "METTL3-IN-14" in MCE Product Catalog:

Cat. No.: HY-187208
Target:  

METTL3 SARS-CoV

Research Areas:  

Infection

METTL3-IN-14 is a METTL3 inhibitor with a target IC50 of 6.68 μM and target Kd of 8.7 μM. METTL3-IN-14 binds to the METTL3 active site, inhibits methyltransferase activity, and does not alter METTL3 mRNA or protein expression levels. METTL3-IN-14 acts as an antiviral agent, exerts anti-SARS-CoV-2 activity via non-METTL3 targets. METTL3-IN-14 can be used for the research of covid-19 .
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20
20 Publications Verification
Cat. No.: HY-19528
CAS No.: 979-92-0
Synonyms: SAH (S-AdenosylhomocysteINe)
SAH (S-Adenosylhomocysteine) is an amino acid derivative and a modulartor in several metabolic pathways. It is an intermediate in the synthesis of cysteine and adenosine . SAH is an inhibitor for METTL3-METTL14 heterodimer complex (METTL3-14) with an IC50 of 0.9 µM .
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3
3 Cited Publications
Cat. No.: HY-W037893
CAS No.: 122323-88-0
Synonyms: Methyl piperazINe-2-carboxylate dihydrochloride; METTL3 activator-1
Target:  

METTL3 HIV

Research Areas:  

Infection Neurological Disease

CHMA1004 (Methyl piperazine-2-carboxylate; METTL3 activator-1) dihydrochloride is a METTL3/METTL14/WTAP methyltransferase complex activator. CHMA1004 dihydrochloride exhibits neuroprotective and anxiolytic potential by enhancing m 6A methylation modification of RNA. CHMA1004 dihydrochloride promotes HIV replication in an infection context. CHMA1004 dihydrochloride can be used in studies related to anxiety disorders and HIV-1 infection .
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2
2 Cited Publications
Cat. No.: HY-160415
CAS No.: 3066823-45-5
Target:  

PROTACs METTL3 Apoptosis

Research Areas:  

Cancer

WD6305 is a potent and selective METTL3-METTL14 PROTAC degrader. WD6305 has DC50 values of 140 nM and 194 nM for METTL3 and METTL14, respectively. WD6305 inhibits m 6A modification and proliferation of AML cells, and induces apoptosis.
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2
2 Cited Publications
Cat. No.: HY-160415A
Target:  

PROTACs METTL3 Apoptosis

Research Areas:  

Cancer

WD6305 TFA is a potent and selective METTL3-METTL14 PROTAC degrader. WD6305 TFA has DC50 values of 140 nM and 194 nM for METTL3 and METTL14, respectively. WD6305 TFA inhibits m 6A modification and proliferation of AML cells, and induces apoptosis. WD6305 TFA has antitumor activity .(Pink: UZH2 (HY-115717); Black: Linker; Blue: VHL ligand (HY-150803))
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2
2 Cited Publications
Cat. No.: HY-153625
CAS No.: 2762286-04-2
Purity:  99.92%
Target:  

METTL3

Research Areas:  

Cancer

STM2120 is a METTL3-METTL14 inhibitor with an IC50 of 64.5 μM .
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1
1 Cited Publications
Cat. No.: HY-P10387
Research Areas:  

Cancer

RSM3 is a METTL3-METTL14 complex inhibitor with a Kd of 3.10 μM for the METTL3-METTL14 complex. RSM3 reduces the m 6A modification level of SLC31A1 and the global RNA methylation level. RSM3 upregulates programmed cell death-related genes, enhances cell apoptosis, inhibits pro-cancer signals and suppresses tumor growth. RSM3 is applicable to the research of preeclampsia and cancer .
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1
1 Cited Publications
Cat. No.: HY-P10387A
Target:  

METTL3 Apoptosis

Research Areas:  

Cancer

RSM3 TFA is a METTL3-METTL14 complex inhibitor with a Kd of 3.10 μM for the METTL3-METTL14 complex. RSM3 TFA reduces the m 6A modification level of SLC31A1 and the global RNA methylation level. RSM3 TFA upregulates programmed cell death-related genes, enhances cell apoptosis, inhibits pro-cancer signals and suppresses tumor growth. RSM3 TFA is applicable to the research of preeclampsia and cancer .
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Cat. No.: HY-19528S
Synonyms: SAH (S-AdenosylhomocysteINe)-d4
SAH-d4 is the deuterium labeled SAH. SAH (S-Adenosylhomocysteine) is an amino acid derivative and a modulartor in several metabolic pathways. It is an intermediate in the synthesis of cysteine and adenosine . SAH is an inhibitor for METTL3-METTL14 heterodimer complex (METTL3-14) with an IC50 of 0.9 μM .
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Cat. No.: HY-19528R
CAS No.: 979-92-0
Synonyms: SAH (S-AdenosylhomocysteINe) (Standard)
SAH (Standard) is the analytical standard of SAH. This product is intended for research and analytical applications. SAH (S-Adenosylhomocysteine) is an amino acid derivative and a modulartor in several metabolic pathways. It is an intermediate in the synthesis of cysteine and adenosine . SAH is an inhibitor for METTL3-METTL14 heterodimer complex (METTL3-14) with an IC50 of 0.9 μM .
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Cat. No.: HY-162282
CAS No.: 3039554-79-2
Target:  

PROTACs METTL3

Research Areas:  

Cancer

PROTAC METTL3-14 degrader 1 is a METTL3-METTL14 heterodimer complex PROTAC degrader. PROTAC METTL3-14 degrader 1 binds to the E3 ubiquitin ligase CRBN, forms a ternary complex with METTL3-METTL14, and promotes the ubiquitination and degradation of METTL3. PROTAC METTL3-14 degrader 1 is applicable to the research of acute myeloid leukemia and prostate cancer .
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Cat. No.: HY-151924
CAS No.: 35940-03-5
Target:  

Enterovirus

Research Areas:  

Infection

Antiviral agent 23 (compound 11b) is an antiviral agent to enterovirus 71 (EV71) with an EC50 value of 94 nM. Antiviral agent 23 effectively suppresses the activity of METTL3/METTL14. Antiviral agent 23 can be used for the research of infection .
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Cat. No.: HY-151926
CAS No.: 23661-03-2
Purity:  99.63%
Target:  

Enterovirus

Research Areas:  

Infection

Antiviral agent 24 is a potent antiviral agent with EC50 values of 0.101, 19.9, 91.2 µM for EV71, CVA21, EV68, respectively. Antiviral agent 24 inhibits METTL3/METTL14 activity in a dose-dependent manner .
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Cat. No.: HY-19528S2
CAS No.: 2687960-02-5
SAH- 13C10 is the 13C labeled SAH . SAH (S-Adenosylhomocysteine) is an amino acid derivative and a modulartor in several metabolic pathways. It is an intermediate in the synthesis of cysteine and adenosine . SAH is an inhibitor for METTL3-METTL14 heterodimer complex (METTL3-14) with an IC50 of 0.9 μM .
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Cat. No.: HY-W125425
CAS No.: 2758-98-7
Synonyms: Methyl piperazINe-2-carboxylate; METTL3 activator-1 free base
Target:  

METTL3 HIV

Research Areas:  

Infection Neurological Disease

CHMA1004 (Methyl piperazine-2-carboxylate; METTL3 activator-1 free base) is a METTL3/METTL14/WTAP methyltransferase complex activator . CHMA1004 exhibits neuroprotective and anxiolytic potential by enhancing m 6A methylation modification of RNA. CHMA1004 promotes HIV replication in an infection context. CHMA1004 can be used in studies related to anxiety disorders and HIV-1 infection .
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Cat. No.: HY-183186
CAS No.: 3050818-07-7
Target:  

METTL3 Cytochrome P450

Research Areas:  

Cancer

EP102 is an orally active, selective inhibitor of the METTL3/METTL14 complex with an IC50 of 2 nM. EP102 reduces intracellular N6-methyladenosine levels, inhibits cancer cell proliferation, and thereby suppresses tumor growth in mouse models. EP102 is applicable for the research of acute myeloid leukemia, ovarian solid tumors and advanced solid tumors .
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