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c-Myc

c-Myc

Myc is a family of regulator genes and proto-oncogenes that code for transcription factors. The Myc family consists of three related human genes: c-myc (MYC), l-myc (MYCL), and n-myc (MYCN). c-myc (also sometimes referred to as MYC) was the first gene to be discovered in this family, due to homology with the viral gene v-myc.
TargetMol
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Cat. No. Product Name CAS No. Purity Chemical Structure
T77939 WBC100
化合物 WBC100
2095780-08-6 98%
TargetMol Chemical Structure WBC100
WBC100(14-D-Valine-TPL),一款高效、选择性和具口服活性的c-Myc小分子降解剂,通过针对泛素E3连结酶CHIP介导的26S蛋白酶体途径实现其作用。主要应用于c-Myc过表达肿瘤的研究领域。
T78055 MYC-RIBOTAC
化合物 MYC-RIBOTAC
98%
TargetMol Chemical Structure MYC-RIBOTAC
MYC-RIBOTAC 是一种针对MYC内部核糖体进入位点(IRES)的核糖核酸酶靶向降解剂(RIBOTAC)。该化合物结合了MYC mRNA的靶向组分以及一种可招募并激活RNA酶L1的小分子。通过降低MYC的mRNA和蛋白质表达水平,MYC-RIBOTAC诱导细胞发生凋亡,应用于抗肿瘤治疗的研究。
T78986 MDEG-541
化合物 MDEG-541
98%
TargetMol Chemical Structure MDEG-541
MDEG-541为一有效MYC-MAX降解剂,展现出显著的抗增殖活性,并有效降低GSPT1、MYC、GSPT2、PLK1蛋白表达水平。
T79438 C-Myc inhibitor 11
化合物 c-Myc inhibitor 11
98%
TargetMol Chemical Structure c-Myc inhibitor 11
c-Myc inhibitor11(Compound 67e),一种c-MYC抑制剂(pEC50: 6.4),在大鼠药代动力学评估中表现出高清除率、中等体积分布和短半衰期,适用于癌症研究领域。
T79439 C-Myc inhibitor 12
化合物 c-Myc inhibitor 12
98%
TargetMol Chemical Structure c-Myc inhibitor 12
c-Myc inhibitor12 (compound 67h),作为c-Myc抑制剂,具有pEC50值为6.4。
T79872 M-Se3
化合物 m-Se3
2829939-44-6 98%
TargetMol Chemical Structure m-Se3
m-Se3 为一选择性c-MYC转录抑制剂,有效抑制肿瘤生长且表现出抗癌活性。
T40419 IRES-C11
化合物IRES-C11
342416-30-2 98%
TargetMol Chemical Structure IRES-C11
IRES-C11 is a specific inhibitor of translation that targets the internal ribosome entry site (IRES) of the c-MYC gene. It functions by blocking the interaction ...
TN3708 Coronarin D
化合物 TN3708
119188-37-3 98%
TargetMol Chemical Structure Coronarin D
Coronarin D shows promising antifungal activity against C. albicans in vitro, the minimum inhibitory concentration (MIC) and the minimum fungicidal concentration...
TN2177 Sanggenol L
桑根醇L
329319-20-2 98%
TargetMol Chemical Structure Sanggenol L
Sanggenol L shows higher cytotoxicity against human oral tumor cell lines (HSC-2 and HSG) than against normal human gingival fibroblasts (HGF), it induces apopto...
TN4582 Moracin T
化合物 TN4582
1146113-27-0 98%
TargetMol Chemical Structure Moracin T
Moracin treatment can inhibit the double 12-O-tetradecanoylphorbol 13-acetate (TPA) treatment-induced morphological changes reflecting inflammatory response, inc...
T16839 SAJM589
化合物 T16839
2089-82-9 98%
TargetMol Chemical Structure sAJM589
sAJM589 is a Myc inhibitor(IC50: 1.8 μM).
T11783 KSI-3716
化合物 T11783
1151813-61-4 98%
TargetMol Chemical Structure KSI-3716
KSI-3716 is an inhibitor of c-Myc.
TN1354 Aaptamine
化合物Aaptamine
85547-22-4 98%
TargetMol Chemical Structure Aaptamine
Aaptamine functions as a proteasome inhibitor, it activates p21 promoter in a p53-independent manner.
T10702 CBP/p300-IN-2
化合物 T10702
2158265-96-2 98%
TargetMol Chemical Structure CBP/p300-IN-2
CBP/EP300-IN-2 is an inhibitor of CBP/EP300 (IC50s: 1.07 nM and 5.96 nM for CBP/HTRF and Myc).
TN4581 Moracin D
化合物 TN4581
69120-07-6 98%
TargetMol Chemical Structure Moracin D
Moracin C and moracin D, new phytoalexins from diseased mulberry, are antifungal compounds. Moracin may be protective influence in tumor promotion, utilization o...
T60019 VPC-70063
化合物VPC-70063
13571-44-3 99.93%
TargetMol Chemical Structure VPC-70063
VPC-70063 (Thiourea, N-[3,5-bis(trifluoromethyl)phenyl]-N'-(phenylmethyl)-) 是 c-Myc-MAX 的抑制剂。 VPC-70063 的 Myc-Max 转录活性抑制率为 106%,IC50 为 8.9 μM,Myc-Max/UBE2C 下游通路抑...
T0617 Nicotinamide N-oxide
烟酰胺-N-氧化物
1986-81-8 99.9%
TargetMol Chemical Structure Nicotinamide N-oxide
Nicotinamide N-oxide (Nicotinamide 1-oxide) 是生物体内烟酰胺分解代谢物,是高效选择性CXCR2受体拮抗剂。
T3048 10058-F4
化合物10058-F4
403811-55-2 99.82%
TargetMol Chemical Structure 10058-F4
10058-F4 (c-Myc Inhibitor) 是一种细胞渗透性噻唑烷酮,可特异性抑制 c-Myc-Max 相互作用并防止 c-Myc 靶基因表达的反式激活;诱导细胞周期停滞和凋亡。
T9093 NY2267
化合物NY2267
886053-73-2 99.6%
TargetMol Chemical Structure NY2267
NY2267 (Acetic acid, 2-[[6-[2-(cyclohexylamino)-1-[[(4-methoxyphenyl)methyl](2-pyridinylcarbonyl)amino]-2-oxoethyl]-2-naphthalenyl]oxy]-, 1,1-dimethylethyl ester...
T4367 Mycro 3
化合物Mycro-3
944547-46-0 99.51%
TargetMol Chemical Structure Mycro 3
Mycro 3 在全细胞分析中对 c-Myc 具有强效选择性,可用于胰腺癌的研究。
WBC100
T77939
WBC100(14-D-Valine-TPL),一款高效、选择性和具口服活性的c-Myc小分子降解剂,通过针对泛素E3连结酶CHIP介导的26S蛋白酶体途径实现其作用。主要应用于c-Myc过表达肿瘤的研究领域。
MYC-RIBOTAC
T78055
MYC-RIBOTAC 是一种针对MYC内部核糖体进入位点(IRES)的核糖核酸酶靶向降解剂(RIBOTAC)。该化合物结合了MYC mRNA的靶向组分以及一种可招募并激活RNA酶L1的小分子。通过降低MYC的mRNA和蛋白质表达水平,MYC-RIBOTAC诱导细胞发生凋亡,应用于抗肿瘤治疗的研究。
MDEG-541
T78986
MDEG-541为一有效MYC-MAX降解剂,展现出显著的抗增殖活性,并有效降低GSPT1、MYC、GSPT2、PLK1蛋白表达水平。
c-Myc inhibitor 11
T79438
c-Myc inhibitor11(Compound 67e),一种c-MYC抑制剂(pEC50: 6.4),在大鼠药代动力学评估中表现出高清除率、中等体积分布和短半衰期,适用于癌症研究领域。
c-Myc inhibitor 12
T79439
c-Myc inhibitor12 (compound 67h),作为c-Myc抑制剂,具有pEC50值为6.4。
m-Se3
T79872
m-Se3 为一选择性c-MYC转录抑制剂,有效抑制肿瘤生长且表现出抗癌活性。
IRES-C11
T40419
IRES-C11 is a specific inhibitor of translation that targets the internal ribosome entry site (IRES) of the c-MYC gene. It functions by blocking the interaction ...
Coronarin D
TN3708
Coronarin D shows promising antifungal activity against C. albicans in vitro, the minimum inhibitory concentration (MIC) and the minimum fungicidal concentration...
Sanggenol L
TN2177
Sanggenol L shows higher cytotoxicity against human oral tumor cell lines (HSC-2 and HSG) than against normal human gingival fibroblasts (HGF), it induces apopto...
Moracin T
TN4582
Moracin treatment can inhibit the double 12-O-tetradecanoylphorbol 13-acetate (TPA) treatment-induced morphological changes reflecting inflammatory response, inc...
sAJM589
T16839
sAJM589 is a Myc inhibitor(IC50: 1.8 μM).
KSI-3716
T11783
KSI-3716 is an inhibitor of c-Myc.
Aaptamine
TN1354
Aaptamine functions as a proteasome inhibitor, it activates p21 promoter in a p53-independent manner.
CBP/p300-IN-2
T10702
CBP/EP300-IN-2 is an inhibitor of CBP/EP300 (IC50s: 1.07 nM and 5.96 nM for CBP/HTRF and Myc).
Moracin D
TN4581
Moracin C and moracin D, new phytoalexins from diseased mulberry, are antifungal compounds. Moracin may be protective influence in tumor promotion, utilization o...
VPC-70063
T60019
VPC-70063 (Thiourea, N-[3,5-bis(trifluoromethyl)phenyl]-N'-(phenylmethyl)-) 是 c-Myc-MAX 的抑制剂。 VPC-70063 的 Myc-Max 转录活性抑制率为 106%,IC50 为 8.9 μM,Myc-Max/UBE2C 下游通路抑...
Nicotinamide N-oxide
T0617
Nicotinamide N-oxide (Nicotinamide 1-oxide) 是生物体内烟酰胺分解代谢物,是高效选择性CXCR2受体拮抗剂。
10058-F4
T3048
10058-F4 (c-Myc Inhibitor) 是一种细胞渗透性噻唑烷酮,可特异性抑制 c-Myc-Max 相互作用并防止 c-Myc 靶基因表达的反式激活;诱导细胞周期停滞和凋亡。
NY2267
T9093
NY2267 (Acetic acid, 2-[[6-[2-(cyclohexylamino)-1-[[(4-methoxyphenyl)methyl](2-pyridinylcarbonyl)amino]-2-oxoethyl]-2-naphthalenyl]oxy]-, 1,1-dimethylethyl ester...
Mycro 3
T4367
Mycro 3 在全细胞分析中对 c-Myc 具有强效选择性,可用于胰腺癌的研究。
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