24 Results for "

PAD1

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

24 Results for "PAD1" in MCE Product Catalog:

24
24 Publications Verification
Cat. No.: HY-100574A
CAS No.: 1373232-26-8
Purity:  99.82%
Cl-amidine hydrochloride is an orally active peptidylarginine deminase (PAD) inhibitor, with IC50 values of 0.8 μM, 6.2 μM and 5.9 μM for PAD1, PAD3, and PAD4, respectively. Cl-amidine hydrochloride induces apoptosis in cancer cells. Cl-amidine hydrochloride induces microRNA (miR)-16 (miRNA-16, microRNA-16) expression and causes cell cycle arrest. Cl-Amidine hydrochloride prevents histone 3 citrullination and neutrophil extracellular trap formation, and improves survival in a murine sepsis model [1] .
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24
24 Publications Verification
Cat. No.: HY-100574B
CAS No.: 1043444-18-3
Cl-amidine TFA is an orally active peptidylarginine deminase (PAD) inhibitor, with IC50 values of 0.8 μM, 6.2 μM and 5.9 μM for PAD1, PAD3, and PAD4, respectively. Cl-amidine TFA induces apoptosis in cancer cells. Cl-amidine TFA induces microRNA (miR)-16 (miRNA-16, microRNA-16) expression and causes cell cycle arrest. Cl-Amidine TFA prevents histone 3 citrullination and neutrophil extracellular trap formation, and improves survival in a murine sepsis model [1] .
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1 Cited Publications
Cat. No.: HY-124586
CAS No.: 3930-19-6
Purity:  99.20%
Synonyms: Bruneomycin
Streptonigrin (Bruneomycin) is an orally active antibiotic and pan-PAD inhibitor, inhibiting PAD1, PAD2, PAD3 and PAD4 with IC50 of 48.3 μM, 26.1 μM, 0.43 μM and 2.5 μM, respectively. Streptonigrin inhibits SENP1 (IC50 of 0.518 μM) and reduces HIF1α. Streptonigrin increases p53 and Apoptosis. Streptonigrin shows antiviral activity against Rauscher murine leukemia virus. Streptonigrin has immunosuppressive effects. Streptonigrin has antitumor activity against osteosarcoma [1] .
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1 Cited Publications
Cat. No.: HY-P790098
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PSMD14; 26S Proteasome Regulatory Subunit RPN11; Proteasome 26S Subunit, Non-ATPase 14; Ubiquitin C-Terminal Hydrolase PSMD14; POH1; Testis Tissue Sperm-Binding Protein Li 69n; 26S Proteasome Non-ATPase Regulatory Subunit 14; 26S Proteasome Regulatory Sub
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Cat. No.: HY-176710
PAD-PF2 is a PAD family inhibitor, as well as a κ-opioid receptor agonist (EC50 = 7.55 μM) and an M1 muscarinic acetylcholine receptor antagonist (IC50 = 12.3 μM). The IC50 values of PAD-PF2 against PAD1, PAD2, PAD3 and PAD4 are 109 nM, 27.9 nM, 106 nM and 20.1 nM, respectively. PAD-PF2 binds to the common allosteric pocket of PAD1-4, and its inhibitory effects on PAD2 and PAD4 are Ca 2+-dependent. PAD-PF2 inhibits protein citrullination in neutrophils. PAD-PF2 is applicable to research related to rheumatoid arthritis, neurodegenerative diseases and cancer [1].
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Cat. No.: HY-100574
CAS No.: 913723-61-2
Cl-amidine is an orally active peptidylarginine deminase (PAD) inhibitor, with IC50 values of 0.8 μM, 6.2 μM and 5.9 μM for PAD1, PAD3, and PAD4, respectively. Cl-amidine induces apoptosis in cancer cells. Cl-amidine induces microRNA (miR)-16 (miRNA-16, microRNA-16) expression and causes cell cycle arrest. Cl-Amidine prevents histone 3 citrullination and neutrophil extracellular trap formation, and improves survival in a murine sepsis model [1] .
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Cat. No.: HY-137655
CAS No.: 1549811-36-0
Purity:  99.23%
Research Areas:  

Cancer

BMS-P5 is a selective and orally active peptidylarginine deiminase 4 (PAD4) inhibitor with an IC50 of 98 nM. BMS-P5 shows selective for PAD4 over PAD1, PAD2, and PAD3. BMS-P5 blocks multiple myeloma (MM)-induced neutrophil extracellular trap (NET) formation and delays progression of MM in a syngeneic mouse model [1].
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Cat. No.: HY-137655A
CAS No.: 1550371-22-6
Purity:  99.93%
Research Areas:  

Cancer

BMS-P5 free base is a selective and orally active peptidylarginine deiminase 4 (PAD4) inhibitor with an IC50 of 98 nM. BMS-P5 free base shows selective for PAD4 over PAD1, PAD2, and PAD3. BMS-P5 free base blocks multiple myeloma (MM)-induced neutrophil extracellular trap (NET) formation and delays progression of MM in a syngeneic mouse model [1].
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Cat. No.: HY-100574D
CAS No.: 2985338-61-0
Purity:  99.91%
Research Areas:  

Cancer

D-Cl-amidine hydrochloride is a potent and highly selective PAD1 inhibitor. D-Cl-amidine is well-torelated with no significant toxicity [1].
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Cat. No.: HY-122365R
CAS No.: 6556-11-2
Synonyms: Inositol niacinate (Standard); Hexanicit (Standard)
Inositol nicotinate (Standard) is the analytical standard of Inositol nicotinate. This product is intended for research and analytical applications. Inositol nicotinate, with vasodilatory effect, is used in the study of Peripheral arterial disease (PAD) .
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Cat. No.: HY-174349
PAD-IN-3 (Compound 16) is a potent dual peptidyl arginine deiminases 4 (PAD4) and PAD1 inhibitor with IC50 values of 0.204 μM and 0.273 μM, respectively. PAD-IN-3 is promising for research of citrullination-associated disorders such as cancer and autoimmune diseases [1].
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Cat. No.: HY-100574C
CAS No.: 1404060-15-6
D-Cl-amidine is a potent and highly selective PAD1 inhibitor. D-Cl-amidine is well-torelated with no significant toxicity [1].
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Cat. No.: HY-137124
CAS No.: 2219331-30-1
Research Areas:  

Cancer

BB-F-Yne is a protein arginine deiminase (PAD) inhibitor with Ki values of PAD1-4.are 2050, 1700, 1100, 3100 M -1min -1 respectively. BB-F-Yne can be used as a click probe to label PAD .
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Cat. No.: HY-137125
CAS No.: 2219324-71-5
Research Areas:  

Cancer

BB-Cl-Yne is a protein arginine deiminase (PAD) inhibitor with Ki values of PAD1-4.are 6400, 3600, 10800, 4900 M -1min -1 respectively. BB-Cl-Yne can be used as a click probe to label PAD .
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Cat. No.: HY-139088
CAS No.: 1671088-84-8
Research Areas:  

Neurological Disease

PAD3-IN-1 (compound 14b) is an inhibitor of protein arginine deiminase (PAD) and is more than 10-fold more selective for PAD3 than PAD 1, 2, and 4. The IC50 values ​​of PAD3-IN-1 for PAD 1, 2, 3, and 4 are 120, 27.5, 4.5, and 30.5 μM, respectively. And PAD3 is a PAD isoform associated with neurodegenerative responses to spinal cord injury, and PAD3-IN-1 could be used to study PAD-related neurological diseases [1].
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Cat. No.: HY-178365
PAD-IN-4 is a potent PAD inhibitor (PAD 1/4, IC50 = 0.273/0.24 μM). PAD-IN-4 shows no significant cytotoxicity against A549 or MDA-MB-231 cells. PAD-IN-4 can be used for the study of cancer and autoimmune diseases [1].
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Cat. No.: HY-P703022
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: PADI1; PDI; Peptidyl Arginine Deiminase 1; Peptidyl Arginine Deiminase, Type I; PDI1; Protein-Arginine Deiminase Type I; PAD1; Peptidylarginine Deiminase I; Protein-Arginine Deiminase Type-1; HPAD-Colony 10; HPAD10; Peptidylarginine Deiminase Type I
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Cat. No.: HY-P704834
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: PADI1; PDI; Peptidyl Arginine Deiminase 1; Peptidyl Arginine Deiminase, Type I; PDI1; Protein-Arginine Deiminase Type I; PAD1; Peptidylarginine Deiminase I; Protein-Arginine Deiminase Type-1; HPAD-Colony 10; HPAD10; Peptidylarginine Deiminase Type I
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Cat. No.: HY-P82505
Synonyms: 26S proteasome non-ATPase regulatory subunit 14; PAD1; POH1; Psmd14; RPN11

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-100574DR
CAS No.: 2985338-61-0
D-Cl-amidine (hydrochloride) (Standard) is the analytical standard of D-Cl-amidine (hydrochloride) (HY-100574D). This product is intended for research and analytical applications. D-Cl-amidine hydrochloride is a potent and highly selective PAD1 inhibitor. D-Cl-amidine is well-torelated with no significant toxicity [1].
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