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Results for "

NRP1

" in MedChemExpress (MCE) Product Catalog:

28

Inhibitors & Agonists

9

Peptides

2

Inhibitory Antibodies

11

Recombinant Proteins

2

Isotope-Labeled Compounds

5

Antibodies

4

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-P99386

    MNRP-1685A

    Complement System EGFR PDGFR p38 MAPK Cancer
    Vesencumab (MNRP-1685A) is IG1 antibody against neuropilin-1 (NRP-1). Vesencumab binds to NRP-1 and prevents the subsequent coupling of NRP-1 to VEGFR-2. Vesencumab has anti-angiogenic and anti-neoplastic activities. Vesencumab can be used in the research of metastatic solid tumors, including ovarian cancer [1] .
    Vesencumab
  • HY-10799
    EG00229 trifluoroacetate
    Maximum Cited Publications
    11 Publications Verification

    Complement System Cancer
    EG00229 is a neuropilin 1 (NRP1) receptor antagonist. EG00229 selectively inhibits VEGF-A binding to NRP1 b1 domain with an IC50 of 3 μM, but has no effect on VEGFA binding to VEGFR-1 and VEGFR-2 [1].
    EG00229 trifluoroacetate
  • HY-112151
    EG01377
    5 Publications Verification

    Complement System Cancer
    EG01377 is a potent, bioavailable and selective inhibitor of neuropilin-1 (NRP1), with a Kd of 1.32 μM, and IC50s of both 609 nM for NRP1-a1 and NRP1-b1. EG01377 has antiangiogenic, antimigratory, and antitumor effects [1].
    EG01377
  • HY-112151A
    EG01377 dihydrochloride
    5 Publications Verification

    Complement System Cancer
    EG01377 dihydrochloride is a potent, bioavailable and selective inhibitor of neuropilin-1 (NRP1), with a Kd of 1.32 μM, and IC50s of 609 nM for both NRP1-a1 and NRP1-b1. EG01377 dihydrochloride has antiangiogenic, antimigratory, and antitumor effects [1].
    EG01377 dihydrochloride
  • HY-133034

    Complement System Cancer
    NRP1 antagonist 1 (compound 12a) is a potent NRP1 antagonist with an IC50 of 19.1 μM. NRP1 antagonist 1 has the potential for cancer research [1].
    NRP1 antagonist 1
  • HY-P3448

    CEND-1; iRGD; LSTA1

    Integrin Complement System Cancer
    Certepetide (CEND-1) is a bifunctional cyclic peptide (a.k.a. iRGD). Certepetide is a tumor-penetrating enhancer via RGD motif interaction with alphav-integrins and via activating NRP-1, and transforms the solid tumor microenvironment into a temporary agent conduit. Certepetide accumulates in tumors, and is used in the research of pancreatic cancer and other solid tumors [1] .
    Certepetide
  • HY-P10787

    Complement System Cancer
    tLyP-1 peptide is an NRP-1 targeting peptide with an IC50 of 4 μM, and its amino acid sequence is CGNKRTR. tLyP-1 peptide specifically binds to NRP-1 to target tumor cells [1].
    tLyP-1 peptide
  • HY-P1663A
    ATWLPPR Peptide TFA
    1 Publications Verification

    Complement System Cardiovascular Disease Metabolic Disease
    ATWLPPR Peptide TFA, a heptapeptide, acts as a selective neuropilin-1 inhibitor, inhibits VEGF165 binding to NRP-1, used in the research of angiogenesis [1]. ATWLPPR Peptide TFA has potential in reducing the early retinal damage caused by diabetes .
    ATWLPPR Peptide TFA
  • HY-P10097

    VEGFR Others
    Flt2-11 is a anti-angiogenic peptide, and specifically binds NRP-1. Flt2-11 inhibits NRP-1/sVEGFR-1 interaction.
    Flt2-11
  • HY-RS16529

    Small Interfering RNA (siRNA) Others

    Nrp1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Nrp1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Nrp1 Mouse Pre-designed siRNA Set A
    Nrp1 Mouse Pre-designed siRNA Set A
  • HY-RS09579

    Small Interfering RNA (siRNA) Others

    NRP1 Human Pre-designed siRNA Set A contains three designed siRNAs for NRP1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    NRP1 Human Pre-designed siRNA Set A
    NRP1 Human Pre-designed siRNA Set A
  • HY-147762

    Complement System Cancer
    NRP1 antagonist 2 (Compound 1) is an NRP1 antagonist [1].
    NRP1 antagonist 2
  • HY-P11286

    Complement System Cancer
    A7RC is a multifunctional peptide used in tumor-targeted therapy, with Cysteine added to the C-terminal of the A7R peptide (sequence: ATWLPPR). A7R (HY-P1663) is a ligand of the NRP-1 receptor, regulating intracellular signal transduction related to tumor vascularization and tumor growth [1].
    A7RC
  • HY-163062

    Microtubule/Tubulin Apoptosis Complement System Cancer
    Tubulin/NRP1-IN-1 (compound TN-2) is a dual inhibitor of Tubulin and NRP1 with IC50s of 0.71 and 0.85 μM, respectively. Tubulin/NRP1-IN-1 significantly inhibits the viability of prostate tumor cell lines and induces apoptosis [1].
    Tubulin/NRP1-IN-1
  • HY-RS22960

    Small Interfering RNA (siRNA) Others

    Nrp1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Nrp1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Nrp1 Rat Pre-designed siRNA Set A
    Nrp1 Rat Pre-designed siRNA Set A
  • HY-P3448S

    CEND-1-13C6,15N2; iRGD-13C6,15N2; LSTA1-13C6,15N2

    Isotope-Labeled Compounds Complement System Integrin Cancer
    Certepetide- 13C6, 15N2 (CEND-1- 13C6, 15N2) is the 13C- and 15N-labeled Certepetide (HY-P3448). Certepetide (CEND-1) is a bifunctional cyclic peptide (a.k.a. iRGD). Certepetide is a tumor-penetrating enhancer via RGD motif interaction with alphav-integrins and via activating NRP-1, and transforms the solid tumor microenvironment into a temporary agent conduit. Certepetide accumulates in tumors, and is used in the research of pancreatic cancer and other solid tumors [1] .
    Certepetide-13C6,15N2
  • HY-P10788

    Complement System Cancer
    CK3 peptide is an NRP-1 targeting peptide with the amino acid sequence CLKADKAKC. The CK3 peptide specifically binds to NRP-1 to target breast cancer cells. Single-photon emission computed tomography (SPECT) and near-infrared fluorescence (NIRF) imaging show significant accumulation of CK3 peptide in xenograft tumors in nude mice. CK3 peptide can be used for molecular imaging studies of breast cancer.
    CK3 peptide
  • HY-128446

    VEGFR Neurological Disease
    CAY10781 (Compound 11) is an inhibitor of the neuropilin-1 (NRP-1) and VEGF-A interaction. CAY10781 inhibits VEGF-A-induced phosphorylation of VEGFR2 in Catecholamine A-differentiated (CAD) cells [1]< sup>.
    CAY10781
  • HY-P991329

    Complement System Cancer
    ASP-1948 is a human monoclonal antibody (mAb) targeting NRP1/VEGF165R/CD34. ASP-1948 reverses the suppressive effects of regulatory T cells. ASP-1948 can be used in solid tumors research [1].
    ASP-1948
  • HY-18333

    VEGFR Cancer
    EG00229 is an inhibitor for VEGF-A and NRP1 interaction with an IC50 of 8 μM. EG00229 inhibits the migration of HUVECS and the phosphorylation of VEGFR2 in endothelial cells. EG00229 exhibits cytotoxicity in cancer cell A549 [1].
    EG00229
  • HY-179350A

    VEGFR Neurological Disease
    EG01449 is a quinoline-based antagonist of Neuropilin-1 (NRP1) with an Kd of 0.6 µM. EG01449 competitively inhibits the binding of VEGFA to NRP1 with an IC50 of 362 nM. EG01449 prevents VEGFA-induced pain by inhibiting NRP1-dependent signaling and reducing sodium currents in sensory neurons. EG01449 can be used for the research of nociceptive pain [1].
    EG01449
  • HY-179350

    VEGFR Neurological Disease
    EG01449 Free acid is a quinoline-based antagonist of Neuropilin-1 (NRP1) with an Kd of 0.6 µM. EG01449 Free acid competitively inhibits the binding of VEGFA to NRP1 with an IC50 of 362 nM. EG01449 Free acid prevents VEGFA-induced pain by inhibiting NRP1-dependent signaling and reducing sodium currents in sensory neurons. EG01449 Free acid can be used for the research of nociceptive pain [1].
    EG01449 Free acid
  • HY-P3448S1

    CEND-1-13C2,15N; iRGD-13C2,15N; LSTA1-13C2,15N

    Isotope-Labeled Compounds Complement System Integrin Cancer
    Certepetide- 13C2, 15N (CEND-1- 13C2, 15N) is the 13C- and 15N-labeled Certepetide (HY-P3448). Certepetide (CEND-1) is a bifunctional cyclic peptide (a.k.a. iRGD). Certepetide is a tumor-penetrating enhancer via RGD motif interaction with alphav-integrins and via activating NRP-1, and transforms the solid tumor microenvironment into a temporary agent conduit. Certepetide accumulates in tumors, and is used in the research of pancreatic cancer and other solid tumors [1] .
    Certepetide-13C2,15N
  • HY-182700

    Complement System VEGFR Cancer
    NRPa-308 is a potent and orally active Neuropilin-1 (NRP-1) antagonist with an IC50 of 42 μM for inhibiting VEGF-A165 binding to NRP-1. NRPa-308 blocks the specific interaction between VEGF-A165 and NRP-1. NRPa-308 effectively suppresses angiogenesis in vitro and in vivo and reduces the viability of a broad spectrum of human solid and haematological cancer cells. NRPa-308 inhibits tumor growth and prolongs median survival in a human breast cancer xenograft mouse model. NRPa-308 can be used for the research of multiple human malignancies including solid tumors and hematological cancers [1].
    NRPa-308
  • HY-10799R

    Reference Standards Complement System Cancer
    EG00229 trifluoroacetate (Standard) is the analytical standard of EG00229 (trifluoroacetate) (HY-10799). This product is intended for research and analytical applications. EG00229 is a neuropilin 1 (NRP1) receptor antagonist. EG00229 selectively inhibits VEGF-A binding to NRP1 b1 domain with an IC50 of 3 μM, but has no effect on VEGFA binding to VEGFR-1 and VEGFR-2 [1].
    EG00229 trifluoroacetate (Standard)
  • HY-P11647A

    Complement System Cancer
    RPARPAR acetate is a CendR tumor-penetrating peptide. RPARPAR acetate directly binds to the NRP-1 and NRP-2 receptors on the surface of tumor cells, triggering cellular internalization, vascular extravasation, and penetration into tumor tissues. RPARPAR acetate serves as an efficient ligand for targeting nanocarriers to NRP-1-positive tumors. RPARPAR acetate is applicable in research on tumor targeting and drug delivery [1].
    RPARPAR acetate
  • HY-P11647

    Complement System Cancer
    RPARPAR is a CendR tumor-penetrating peptide. RPARPAR directly binds to the NRP-1 and NRP-2 receptors on the surface of tumor cells, triggering cellular internalization, vascular extravasation, and penetration into tumor tissues. RPARPAR serves as an efficient ligand for targeting nanocarriers to NRP-1-positive tumors. RPARPAR is applicable in research on tumor targeting and drug delivery [1].
    RPARPAR
  • HY-RS09204

    Small Interfering RNA (siRNA) Others

    NELL1 Human Pre-designed siRNA Set A contains three designed siRNAs for NELL1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    NELL1 Human Pre-designed siRNA Set A
    NELL1 Human Pre-designed siRNA Set A

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