29 Results for "

P15

" in MedChemExpress (MCE) Product Catalog:
Products (29)

29 Results for "P15" in MCE Product Catalog:

21
21 Cited Publications
Cat. No.: HY-108496
CAS No.: 26993-30-6
Purity:  ≥99.0%
Synonyms: S1P
Sphingosine-1-phosphate (S1P) is an agonist of S1P1-5 receptors and a ligand of GPR3, GPR6 and GPR12. Sphingosine-1-phosphate is an intracellular second messenger and mobilizes Ca 2+ as an extracellular ligand for G protein-coupled receptors . Sphingosine-1-phosphate is an important lipid mediator generated from Sphingomyelin (HY-113498) or other membrane phospholipids . Sphingosine-1-phosphate stimulates the DNA synthesis, cell proliferation and migration .
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Cat. No.: HY-P11087
CAS No.: 134335-45-8
Target:  

Collagen

Research Areas:  

Others

P15 is a collagen mimetic peptide with the sequence of GTPGPQGIAGQRGVV. P15 can mimic the cell-binding domain of human type I collagen. P15 is capable of promoting the adhesion, proliferation, and differentiation of osteoblasts. Biomaterials modified with P15 can be used in research related to bone regeneration .
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Cat. No.: HY-P3333
CAS No.: 153049-05-9
Target:  

MHC

Research Areas:  

Inflammation/Immunology Cancer

KSPWFTTL is an immunodominant Kb-restricted epitope from the p15E transmembrane protein. KSPWFTTL can restore susceptibility of a tumor line to anti-AKR/Gross MuLV cytotoxic T lymphocytes .
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Cat. No.: HY-108496S
CAS No.: 2260670-15-1
Purity:  99.00%
Synonyms: S1P-d7
Sphingosine-1-phosphate-d7 is the deuterium labeled Sphingosine-1-phosphate. Sphingosine-1-phosphate (S1P) is an agonist of S1P1-5 receptors and a ligand of GPR3, GPR6 and GPR12.?Sphingosine-1-phosphate is an intracellular second messenger and mobilizes Ca2+ as an extracellular ligand for G protein-coupled receptors . Sphingosine-1-phosphate is an important lipid mediator generated from Sphingomyelin (HY-113498) or other membrane phospholipids .
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Cat. No.: HY-P4056A
Synonyms: P15-Tat acetate
Target:  

Casein Kinase Apoptosis

Research Areas:  

Cancer

CIGB-300 acetate (P15-Tat acetate) is an anti-casein kinase 2 (CK2) peptide that exhibits anticancer properties by interfering with the phosphorylation of protein kinase CK2. CIGB-300 acetate induces apoptosis in multiple tumor cell lines and can be used in cancer research .
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Cat. No.: HY-P10365
Research Areas:  

Others

Vmm-p15 is a peptide agonist optimized for the adhesion G protein-coupled receptor GPR64 (also known as ADGRG2 or HE6). The affinity of VPM-p15 with GPR64 is significantly higher than that of the original p15 peptide. The cAMP level induced by VMM-P15 increased significantly, activated GPR64, and triggered downstream Gs, Gq, and G12/13 signaling. VPM-p15 can be used to study the activation mechanism of adherent GPCR family members .
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Cat. No.: HY-P4056
CAS No.: 1072877-99-6
Synonyms: P15-Tat
Target:  

Casein Kinase Apoptosis

Research Areas:  

Cancer

CIGB-300 (P15-Tat) is an anti-casein kinase 2 (CK2) peptide that exhibits anticancer properties by interfering with the phosphorylation of protein kinase CK2. CIGB-300 induces apoptosis in multiple tumor cell lines and can be used in cancer research .
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Cat. No.: HY-179909
CAS No.: 871701-39-2
Target:  

MEK CDK

Research Areas:  

Cancer

MEK-IN-9 (Compound 4-82) is a MEK inhibitor. MEK-IN-9 induces p15 and p27 protein. MEK-IN-9 can be used in the research of renal adenocarcinoma and colorectal cancer .
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Cat. No.: HY-RS16621
Research Areas:  

Others

Fabp4 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Fabp4 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P3333A
Target:  

MHC

Research Areas:  

Inflammation/Immunology Cancer

KSPWFTTL TFA is an immunodominant Kb-restricted epitope from the p15E transmembrane protein. KSPWFTTL TFA can restore susceptibility of a tumor line to anti-AKR/Gross MuLV cytotoxic T lymphocytes .
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Cat. No.: HY-126048
CAS No.: 871696-49-0
Target:  

MEK

Research Areas:  

Cancer

JTP-70902, a p15 INK4b-inductive compound, is a MEK1/2 inhibitor. JTP-70902 exhibits potent antitumor effect .
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Cat. No.: HY-170970
Target:  

Bacterial

Research Areas:  

Infection

Mtb-IN-10 (Compound P15) is a Rv1625c/Cya activator that regulates cAMP metabolism to influence the growth of Mycobacterium tuberculosis (Mtb). Mtb-IN-10 exhibits an EC50 of 1.96 µM in an Mtb-infected macrophage model and demonstrates 58.0% oral bioavailability in mice at a 20 mg/kg dose. It may regulate intracellular signaling and disrupt cholesterol metabolism in Mtb, thereby inhibiting bacterial proliferation. Mtb-IN-10 holds potential for tuberculosis (TB) research, particularly for combating multidrug-resistant (MDR-TB) and extensively drug-resistant (XDR-TB) Mtb strains .
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Cat. No.: HY-P85850

Host:  

Mouse

Application:  

WB, ICC/IF, ELISA

Reactivity:  

Human

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Cat. No.: HY-RS27622
Research Areas:  

Others

Cdkn2b Rat Pre-designed siRNA Set A contains three designed siRNAs for Cdkn2b gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Cat. No.: HY-P701328
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: BH3-interacting domain death agonist; BID; P15 BID
Species:  
Source:  
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Cat. No.: HY-RS09720
Research Areas:  

Others

NXT1 Human Pre-designed siRNA Set A contains three designed siRNAs for NXT1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P72852
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: BH3-interacting domain death agonist; BID; P15 BID
Species:  
Source:  
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Cat. No.: HY-RS13999
Research Areas:  

Others

SUB1 Human Pre-designed siRNA Set A contains three designed siRNAs for SUB1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS02416
Research Areas:  

Others

CDKN2B Human Pre-designed siRNA Set A contains three designed siRNAs for CDKN2B gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-14433A
CAS No.: 1149727-65-0
Synonyms: (S)-PF-991
Target:  

LPL Receptor

Research Areas:  

Inflammation/Immunology

(S)-PF-462991 is a direct-acting S1P1,5 agonist .
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