24 Results for "

L-dC

" in MedChemExpress (MCE) Product Catalog:
Products (24)

24 Results for "L-dC" in MCE Product Catalog:

23
23 Publications Verification
Cat. No.: HY-111674
CAS No.: 2407782-01-6
Purity:  99.51%
Target:  

Pyroptosis

Research Areas:  

Inflammation/Immunology

LDC7559 is a gasdermin D (GSDMD) inhibitor via blocking neutrophil extracellular trap (NET) in the late stages .
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13
13 Cited Publications
Cat. No.: HY-15878
CAS No.: 1073485-20-7
Purity:  98.09%
Synonyms: LdC067
Target:  

CDK Apoptosis

Research Areas:  

Cancer

LDC000067 is a highly specific CDK9 inhibitor with an IC50 value of 44±10 nM in vitro.
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11
11 Cited Publications
Cat. No.: HY-137067
CAS No.: 2304621-06-3
Purity:  99.45%
Synonyms: LdC203974
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

IMT1B (LDC203974) is an orally active, noncompetitive and specific allosteric inhibitor of mitochondrial RNA polymerase (POLRMT) and inhibits mitochondrial DNA (mtDNA) expression. IMT1B has anti-tumour effects .
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11
11 Cited Publications
Cat. No.: HY-12653
CAS No.: 1453834-21-3
Purity:  98.14%
Target:  

CDK HIV HSV

Research Areas:  

Infection

LDC4297 is a selective inhibitor of CDK7 with an IC50 value of 0.13 nM. LDC4297 inhibits human cytomegalovirus (HCMV) replication with an EC50 value of 24.5 nM. LDC4297 shows broad antiviral activities to Herpesviridae, Adenoviridae, Poxviridae, Retroviridae and Orthomyxoviridae with EC50 value of 0.02-1.21 μM. LDC4297 can be used for the research of infection .
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11
11 Cited Publications
Cat. No.: HY-12653A
CAS No.: 2319747-14-1
Purity:  98.23%
Target:  

CDK HIV HSV

Research Areas:  

Infection

LDC4297 hydrochloride is a selective inhibitor of CDK7 with an IC50 value of 0.13 nM. LDC4297 hydrochloride inhibits human cytomegalovirus (HCMV) replication with an EC50 value of 24.5 nM. LDC4297 hydrochloride shows broad antiviral activities to Herpesviridae, Adenoviridae, Poxviridae, Retroviridae and Orthomyxoviridae with EC50 values of 0.02-1.21 μM. LDC4297 hydrochloride can be used for the research of infection .
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10
10 Cited Publications
Cat. No.: HY-12494
CAS No.: 1361030-48-9
Purity:  99.64%
Target:  

TAM Receptor FLT3

Research Areas:  

Neurological Disease Cancer

LDC1267 is a AXL/TAM/FLT3 inhibitor with IC50 values of 42 nM, 130 nM, and 63 nM against AXL, MERTK, and TYRO3, respectively. LDC1267 blocks GAS6-induced AXL phosphorylation and the downstream AKT/ERK1/2 signaling pathway. LDC1267 inhibits cancer cell proliferation, colony formation, and glioblastoma cell invasion, without causing obvious impairment of cytotoxic autophagic flux. LDC1267 exerts a synergistic effect when used in combination with Imatinib (HY-15463) in chronic myeloid leukemia models. LDC1267 can be widely applied in studies related to glioblastoma and chronic myeloid leukemia .
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Cat. No.: HY-P10762
CAS No.: 2082631-84-1
Synonyms: CBP-1008; LdC 10B
Ricorfotide vedotin (CBP-1008) is a dual-ligand peptide-drug conjugate (PDC) conjugated to MMAE (HY-15162), targeting Folate receptor α (FRα) and TRPV6. Ricorfotide vedotin binds to FRα with high affinity and TRPV6 with low affinity. Ricorfotide vedotin has antitumor activity, and can be used in advanced solid tumor research (eg: colorectal cancer, breast cancer, non-small cell lung cancer, ovarian cancer, adrenocortical carcinoma and follicular dendritic cell sarcoma) .
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Cat. No.: HY-121513
CAS No.: 40093-94-5
Purity:  99.61%
Synonyms: 2'-Deoxy-L-cytidine; L-dC
Target:  

HBV

Research Areas:  

Infection

Torcitabine (2'-Deoxy-L-cytidine) is an antiviral agent. Torcitabine has the potential for chronic hepatitis B virus infection treatment .
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Cat. No.: HY-18969
CAS No.: 1453833-30-1
Target:  

CDK

Research Areas:  

Cancer

LDC3140 is a selective CDK7 inhibitor (IC50<5 nM). By inhibiting the activity of CDK7, LDC3140 affects the regulation of the cell cycle, leading to cell cycle arrest and thus inhibiting the proliferation of tumor cells. LDC3140 can be used in the research of cancer treatment .
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Cat. No.: HY-146262
CAS No.: 2411874-83-2
Target:  

EGFR

Research Areas:  

Cancer

LDC0496 is a potent and selective EGFR inhibitor. LDC0496 possesses intense inhibitory potency toward EGFR and Her2 exon20 insertion mutations, as well as selectivity over wild type EGFR and within the kinome .
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Cat. No.: HY-106205
CAS No.: 380886-96-4
Target:  

HBV

Research Areas:  

Infection

Di-Val-L-dC, a prodrug of L-deoxycytidine, is a selective and specific anti-HBV agent .
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Cat. No.: HY-RS07891
Research Areas:  

Others

LUM Human Pre-designed siRNA Set A contains three designed siRNAs for LUM gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS17525
Research Areas:  

Others

Lum Mouse Pre-designed siRNA Set A contains three designed siRNAs for Lum gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-111674R
CAS No.: 2407782-01-6
Research Areas:  

Inflammation/Immunology

LDC7559 (Standard) is the analytical standard of LDC7559 (HY-111674). This product is intended for research and analytical applications. LDC7559 is a gasdermin D (GSDMD) inhibitor via blocKing neutrophil extracellular trap (NET) in the late stages .
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Cat. No.: HY-184315
CAS No.: 2411873-31-7
LDC8201 is a selective, orally active, covalent inhibitor that targets EGFR and Her2 exon 20 insertion mutants. LDC8201 induces tumor shrinkage and regression. LDC8201 is applicable to research related to non-small cell lung cancer carrying EGFR or Her2 exon 20 insertion mutations .
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Cat. No.: HY-P700387
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Constitutive lysine decarboxylase; EC:4.1.1.18; LdCC; ldCC; ldC; ldCH; b0186 ; JW0181
Species:  
Source:  
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Cat. No.: HY-P70369
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: LUM; Keratan Sulfate Proteoglycan Lumican; Prev. LdC; KSPG Lumican; SLRR2D; Epididymis Secretory Sperm Binding Protein; Lumican; Lumican Proteoglycan
Species:  
Source:  
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Cat. No.: HY-P84813
Synonyms: CDSIGN; CLEC4L; dC-SIGN; dC-SIGN1

Host:  

Mouse

Application:  

WB, FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-P84813A
Synonyms: CDSIGN; CLEC4L; dC-SIGN; dC-SIGN1

Host:  

Mouse

Application:  

WB, FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-P70370
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: LUM; Keratan Sulfate Proteoglycan Lumican; Prev. LdC; KSPG Lumican; SLRR2D; Epididymis Secretory Sperm Binding Protein; Lumican; Lumican Proteoglycan
Species:  
Source:  
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