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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
132 Results for "
T4
" in MedChemExpress (MCE) Product Catalog:
Products (132)
132 Results for "T4" in MCE Product Catalog:
Cat. No.: HY-P99436
CAS No.: 1370261-50-9
Synonyms: ABR-214936
Target:
Research Areas:
Cat. No.: HY-12926
CAS No.: 1428535-92-5
Target:
Research Areas:
ST7612AA1 is a histone deacetylase (HDAC) inhibitor that controls chromatin condensation and DNA transcription by removing acetyl groups from histones. ST7612AA1 is also a potent HIV reactivation inducer, and its reactivation activity is exerted without activating or proliferating CD4+T cells, and can be used in the study of HIV reactivation strategies and elimination of viral reservoirs .
Cat. No.: HY-P86915
Synonyms: CD 4 antibody; CD4 (L3T4) antibody; CD4 antibody; CD4 antigen (p55) antibody; CD4 antigen antibody; CD4 molecule antibody; CD4 receptor antibody; CD4+ Lymphocyte deficiency, included antibody; CD4_HUMAN antibody; CD4mut antibody; CD 4 antibody; CD4 (L3T4) antibody; CD4 antibody; CD4 antigen (p55) antibody; CD4 antigen antibody; CD4 molecule antibody; CD4 receptor antibody; CD4+ Lymphocyte deficiency, included antibody; CD4_HUMAN antibody; CD4mut antibody; L3T4 antibody; Leu3 antibody; Ly-4 antibody; Lymphocyte antigen CD4 antibody; MGC165891 antibody; OTTHUMP00000238897 antibody; p55 antibody
Cat. No.: HY-P7630
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: B4GALT4; Beta-1,4-GalTase 4; Beta-1,4-Galactosyltransferase 4; Nal Synthase; Beta4Gal-T4; B4Gal-T4; UDP-Galactose:Beta-N-Acetylglucosamine Beta-1,4-Galactosyltransferase 4; Beta-N-Acetylglucosaminyl-Glycolipid Beta-1,4-Galactosyltransferase 4; UDP-Gal:Bet
Species:
Human
Source:
HEK293
Cat. No.: HY-P72068
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ABAT; GABA-T; 4-Aminobutyrate Aminotransferase; Gamma-Aminobutyrate Aminotransferase; GABAT; 4-Aminobutyrate Transaminase; 4-Aminobutyrate Aminotransferase, Mitochondrial; GABA-AT; (S)-3-Amino-2-Methylpropionate Transaminase; L-AIBAT; Gamma-Amino-N-Butyra
Species:
Human
Source:
E. coli
Cat. No.: HY-150684
CAS No.: 3031654-49-3
Target:
Research Areas:
GXH-II-052 is a potent bivalent bromodomain and extraterminal domain (BET) inhibitor. GXH-II-052 shows binding potential for BRD4-1, BRD4-2, BRD4-T, BRDT-1, BRDT-2, BRDT-T with Kd values of 28, 9.1, 4.8, 0.6, 8.4, 2.6 nM, respectively. GXH-II-052 shows antiproliferative activity. GXH-II-052 decreases the expression of c-Myc .
Cat. No.: HY-150683
CAS No.: 3031654-46-0
Target:
Research Areas:
NC-III-49-1 is a potent bivalent bromodomain and extraterminal domain (BET) inhibitor. NC-III-49-1 shows binding potential for BRD4-1, BRD4-2, BRD4-T, BRDT-1, BRDT-2, BRDT-T with Kd values of 0.095, 0.32, 0.29, 0.089, 5.5, 0.058 nM, respectively. NC-III-49-1 shows antiproliferative activity. NC-III-49-1 decreases the expression of c-Myc .
Cat. No.: HY-W181026
CAS No.: 1197834-98-2
Target:
Research Areas:
KLF10-IN-1 (#48-15) is a KLF10 inhibitor with an IC50 value of 40 μM for KLF10 reporter gene. KLF10-IN-1 can inhibit KLF10-DNA binding and transcriptional activity, block the conversion of CD4+CD25 T cells to CD4+CD25+T regulatory cells, and inhibit the expression of KLF10 target genes. KLF10-IN-1 can be used as a useful mechanistic probe to study KLF10-mediated effects and T regulatory cell biology .
Target:
Research Areas:
Duostatin 5 is a ADC Cytotoxin designed based on MMAF (HY-15579) and can be used to synthesize ADCs. The preparation of Duostatin 5 has the advantages of fewer synthetic steps, simple operation, less difficulty in quality control, and more stable chemical synthesis process. Duostatin 5 can be linked to the antibody targeting 5T4 (ZV05) by cross-linking with interchain cysteines through a disubstituted C-Lock linker. Duostatin 5 is a click chemistry reagent. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-driven alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups[1][2].
Cat. No.: HY-P71142
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: SERPINB3; Serpin Peptidase Inhibitor, Clade B (Ovalbumin), Member 3; Prev. SCCA1; Serpin B3; Prev. SCC; SCCA-1; Squamous Cell Carcinoma Antigen 1; SCCA-PD; HsT1196; SSCA1; T4-A; SCCA; Serine (Or Cysteine) Proteinase Inhibitor, Clade B (Ovalbumin), Member
Species:
Human
Source:
HEK293
Cat. No.: HY-145149S
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
