Ras

Ras inhibitors and related small GTPase modulators act on KRAS and on the Rac, Rho and Cdc42 proteins. Small GTPases of the Ras superfamily work as molecular switches. They cycle between an active form bound to guanosine triphosphate (GTP) and an inactive form bound to guanosine diphosphate (GDP). Oncogenic KRAS mutations such as G12C keep the protein in its signaling state. ARS-853 and KRas G12C inhibitor 4 target the mutant cysteine of KRAS G12C, while Kobe2602 interferes with binding of Ras to Raf. Salirasib, a farnesylcysteine mimetic, disrupts the membrane association of Ras. Rho-family tools include NSC 23766 and EHT 1864, which inhibit Rac, and CASIN, which targets Cdc42.

Items 301-325 of 427

  • KRAS G12D-IN-32
    Cat. No.
    A63657

    KRAS G12D-IN-32

    KRAS G12D-IN-32 is a selective inhibitor of the KRAS G12D mutant protein, which plays a critical role in various oncogenic pathways. This compound is instrumental for investigating the molecular mechanisms underlying adenocarcinoma, colorectal cancer, and non-small cell lung cancer. Researchers can employ KRAS G12D-IN-32 to explore therapeutic strategies targeting KRAS mutations and to evaluate potential treatment responses in cancer models.

    Out of stock

    All 3 sizes
  • 8-pCPT-2′-O-Me-cAMP
    Cat. No.
    A63658

    8-pCPT-2′-O-Me-cAMP

    Synonyms: 8-CPT-2'-O-Me-cAMP

    8-pCPT-2′-O-Me-cAMP is a selective activator of exchange proteins activated by cAMP (Epac), specifically targeting Epac1 with an EC50 of 2.2 μM. This compound does not activate protein kinase A (PKA) with an EC50 greater than 10 μM. 8-pCPT-2′-O-Me-cAMP effectively stimulates Epac-mediated Ca2+ release in pancreatic β-cells in vitro, and it plays a role as a Rap1 activator. Additionally, it enhances the barrier function of retinal pigment epithelium against choroidal endothelial cell invasion, potentially providing insights into therapeutic mechanisms for macular degeneration.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • KRASG12C IN-17
    Cat. No.
    A63659

    KRASG12C IN-17

    KRASG12C IN-17 is an orally active covalent inhibitor targeting the KRASG12C mutation. It demonstrates potent inhibitory effects on KRASG12C-mutant cancer cell lines, with IC50 values of 0.7 nM in NCI-H23 and 0.5 nM in NCI-H358. This compound irreversibly binds to KRASG12C, achieving over 96% modification efficiency in both GDP-bound and GMPPNP-bound states. KRASG12C IN-17 is valuable for research focused on KRAS-driven malignancies, particularly in the context of colorectal cancer.

    Out of stock

    All 3 sizes
  • KRAS G12C inhibitor 35
    Cat. No.
    A63660

    KRAS G12C inhibitor 35

    KRAS G12C inhibitor 35 is a selective inhibitor targeting the KRAS G12C mutation, a driver mutation frequently associated with various cancers. This compound effectively disrupts KRAS signaling pathways, leading to inhibition of tumor cell proliferation. It serves as a valuable tool for research into KRAS G12C-mediated oncogenesis and therapeutic strategies in cancer treatment.

    25 mg
    $1,780.00
    50 mg
    $2,280.00
    All 3 sizes
  • KRAS G12C inhibitor 30
    Cat. No.
    A63662

    KRAS G12C inhibitor 30

    KRAS G12C inhibitor 30 is a selective inhibitor targeting the KRAS G12C mutation. This compound demonstrates significant anti-tumor activity by disrupting the downstream signaling pathways associated with oncogenic KRAS. It is primarily utilized in cancer research, particularly in studies focused on therapies for KRAS-driven malignancies.

    25 mg
    $1,800.00
    50 mg
    $2,285.00
    All 3 sizes
  • PPI stabilizer-1
    Cat. No.
    A63664

    PPI stabilizer-1

    PPI stabilizer-1 is a KRAS dimerizing agent that effectively promotes the dimerization of KRAS with a dissociation constant (KD) of 3.8 µM. This compound has the ability to co-crystallize with GCP-KRASG12D, facilitating structural studies and elucidating the role of KRAS in cellular signaling. PPI stabilizer-1 is valuable for researching KRAS-driven cancers, providing insights into therapeutic strategies targeting this critical pathway.

    Out of stock

    All 3 sizes
  • KRAS ligand 3
    Cat. No.
    A63667

    KRAS ligand 3

    KRAS Ligand 3 is a target-binding ligand for KRAS that interacts with the KRAS inhibitor, enhancing its efficacy. This compound demonstrates synergistic effects in tumor growth inhibition, making it a valuable tool for research in cancer biology and therapeutic development. Its application in studying KRAS-related signaling pathways can provide insights into tumorigenesis and potential treatment strategies.

    Out of stock

    All 3 sizes
  • K-Ras-IN-2
    Cat. No.
    A63669

    K-Ras-IN-2

    K-Ras-IN-2 is a selective antagonist of the K-Ras protein. It has demonstrated significant biological activity in inhibiting K-Ras-driven signaling pathways, making it a valuable tool for researchers studying tumor biology and oncogenic signaling. This compound is particularly useful in cancer research applications focused on K-Ras-related malignancies.

    Out of stock

    All 3 sizes
  • COTI-219
    Cat. No.
    A63671

    COTI-219

    COTI-219 is an orally active inhibitor of the KRAS protein, targeting its role in oncogenic signaling pathways. This compound exhibits significant antitumor activity, making it a valuable tool for cancer research. COTI-219 is utilized in studies aimed at understanding KRAS-related signaling mechanisms and evaluating therapeutic strategies for KRAS-driven tumors.

    Out of stock

    All 3 sizes
  • KRAS G12C inhibitor 48
    Cat. No.
    A63672

    KRAS G12C inhibitor 48

    KRAS G12C Inhibitor 48 is a potent inhibitor targeting the KRAS G12C mutation, with an IC50 of 639.91 nM. This compound demonstrates significant anti-proliferative activity in various cancer cell lines, exhibiting IC50 values of 0.796 µM in H358, 6.33 µM in H23, and 16.14 µM in A549 cells. It serves as a valuable tool for research into KRAS-driven malignancies and therapeutic strategies targeting mutant KRAS.

    Out of stock

    All 3 sizes
  • KRAS G12C inhibitor 59
    Cat. No.
    A63673

    KRAS G12C inhibitor 59

    KRAS G12C inhibitor 59 selectively targets the KRAS G12C mutant protein, inhibiting its downstream signaling pathways. This compound exhibits significant anticancer activity, making it a valuable tool for research focused on KRAS-driven malignancies. It holds potential for further exploration in therapeutic applications against cancers harboring the KRAS G12C mutation.

    Out of stock

    All 3 sizes
  • KRAS G12C inhibitor 23
    Cat. No.
    A63674

    KRAS G12C inhibitor 23

    KRAS G12C inhibitor 23 is a selective inhibitor targeting the KRAS G12C mutation. It effectively inhibits H358 cells with an IC50 value of 491 nM, demonstrating its potential in cancer research. This compound is primarily utilized in studies focused on KRAS-driven cancers for therapeutic development and efficacy evaluation.

    Out of stock

    All 3 sizes
  • KRAS G12C inhibitor 25
    Cat. No.
    A63675

    KRAS G12C inhibitor 25

    KRAS G12C Inhibitor 25 primarily targets the KRAS G12C mutant by inhibiting the SOS1-assisted GDP/GTP exchange activity, demonstrating an IC50 of 0.48 nM. This compound has potential applications in therapeutic research aimed at KRAS-driven cancers, providing a valuable tool for studying the role of KRAS mutations in tumorigenesis and evaluating potential treatment strategies.

    25 mg
    $1,800.00
    50 mg
    $2,285.00
    All 3 sizes
  • KRAS G12D inhibitor 15
    Cat. No.
    A63676

    KRAS G12D inhibitor 15

    KRAS G12D Inhibitor 15 is a selective inhibitor targeting the KRAS G12D mutation, a critical player in various cancer pathways. This compound demonstrates significant potential in studies related to cancer progression and metastasis. Additionally, KRAS G12D Inhibitor 15 features an alkyne moiety, enabling its use in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions, making it a valuable tool for chemical biology applications.

    Out of stock

    All 3 sizes
  • pan-KRAS-IN-17
    Cat. No.
    A63677

    pan-KRAS-IN-17

    pan-KRAS-IN-17 is a potent inhibitor targeting pan-KRAS. This compound effectively disrupts KRAS signaling pathways, demonstrating significant activity in various cancer models characterized by KRAS mutations. It is a valuable tool for research into KRAS-driven malignancies and for investigating therapeutic approaches aimed at inhibiting malignant cell proliferation and survival.

    Out of stock

    All 3 sizes
  • KRAS G12D inhibitor 11
    Cat. No.
    A63678

    KRAS G12D inhibitor 11

    KRAS G12D inhibitor 11 is a potent inhibitor targeting the KRAS G12D mutation, a critical driver of various cancers. This compound interferes with the signaling pathways mediated by the Ras family of proteins, which are essential for cellular proliferation and survival. KRAS G12D inhibitor 11 is applicable in research focused on KRAS G12D-mediated oncogenesis and therapeutic development for related malignancies.

    25 mg
    $2,535.00
    50 mg
    $3,265.00
    All 3 sizes
  • StRIP16
    Cat. No.
    A63679

    StRIP16

    StRIP16 is a bioavailable analogue of StRIP3 that functions as a Ras inhibitor. This double-stapled peptide exhibits high specificity for Rab8a GTPase, with a dissociation constant (Kd) of 12.7 μM. StRIP16 is utilized in research to investigate the role of Rab8a in cellular signaling pathways and its implications in various cancer models.

    Out of stock

    All 3 sizes
  • ISIS 2503
    Cat. No.
    A63682

    ISIS 2503

    ISIS 2503 is a 20-mer antisense oligonucleotide specifically designed to inhibit the expression of Ha-Ras. By targeting the mRNA of Ha-Ras, ISIS 2503 effectively reduces its protein levels, thereby modulating downstream signaling pathways associated with cell proliferation and survival. This reagent is valuable for research applications focused on cancer biology and the study of oncogenic signaling mechanisms.

    Out of stock

    All 3 sizes
  • pan-KRAS-IN-3
    Cat. No.
    A63683

    pan-KRAS-IN-3

    pan-KRAS-IN-3 is a pan-KRAS inhibitor designed to target and inhibit KRAS signaling pathways, which are commonly implicated in various cancers. This compound serves as a useful tool for cancer research by effectively blocking KRAS activity, thereby offering insights into tumor biology and potential therapeutic strategies. Additionally, pan-KRAS-IN-3 features an alkyne group enabling its participation in copper-catalyzed azide-alkyne cycloaddition (CuAAc), facilitating the development of novel chemical probes and conjugates in experimental studies.

    Out of stock

    All 3 sizes
  • KRAS G12D inhibitor 19
    Cat. No.
    A63684

    KRAS G12D inhibitor 19

    KRAS G12D inhibitor 19 is a selective inhibitor targeting the KRAS G12D mutant protein, which plays a pivotal role in driving oncogenic signaling pathways in various cancers. This compound exhibits significant anti-proliferative activity against KRAS G12D-driven tumor cell lines. It serves as a valuable tool in cancer research, particularly for studying the efficacy of KRAS-targeted therapies and understanding the mechanistic pathways involved in KRAS-related malignancies.

    Out of stock

    All 3 sizes
  • Rho GTPase inhibitor 1
    Cat. No.
    A63686

    Rho GTPase inhibitor 1

    Rho GTPase Inhibitor 1 is a selective inhibitor targeting Rho GTPases, with demonstrated high affinity for Cdc42, Rac1, and RhoA, exhibiting KDs of 151, 352, and 232 μM, respectively. This compound effectively reduces cell migration in glioma cell lines, highlighting its potential utility in cancer research and therapeutic development. Its role in modulating Rho GTPase signaling makes it a valuable tool for investigating cellular processes such as motility and invasion.

    Out of stock

    All 3 sizes
  • KRAS-IN-48
    Cat. No.
    A63688

    KRAS-IN-48

    KRAS-IN-48 is a selective inhibitor targeting KRAS mutations, exhibiting Kd values of 2.58 nM for the KRAS-G12D variant and 5.49 μM for KRAS-G12V. This compound demonstrates significant biological activity against KRAS mutant proteins, making it an important tool in cancer research. KRAS-IN-48 is particularly valuable for studies focused on understanding the role of KRAS mutations in tumorigenesis and therapeutic response.

    Out of stock

    All 3 sizes
  • KRAS G12C inhibitor 57
    Cat. No.
    A63689

    KRAS G12C inhibitor 57

    KRAS G12C Inhibitor 57 is a selective and covalent inhibitor targeting the KRAS G12C mutation, exhibiting an IC50 of 0.21 μM in KRAS G12C/SOS1 binding assays. This compound effectively induces apoptosis in cancer cells, making it a valuable tool for studying KRAS-driven malignancies. Its oral bioavailability enhances its suitability for in vivo research applications focused on cancer therapeutics targeting KRAS mutations.

    Out of stock

    All 3 sizes
  • KRAS G12D inhibitor 6
    Cat. No.
    A63690

    KRAS G12D inhibitor 6

    KRAS G12D inhibitor 6 is a selective inhibitor targeting the KRAS G12D mutant, a significant oncogenic driver in various cancers. This compound demonstrates strong inhibitory activity that can facilitate the study of KRAS-mediated signaling pathways and tumor progression. It serves as a valuable tool in cancer research, particularly in developing targeted therapies against KRAS-driven malignancies.

    5 mg
    $795.00
    All 1 sizes
  • KRAS inhibitor-37
    Cat. No.
    A63691

    KRAS inhibitor-37

    KRAS Inhibitor-37 targets the KRAS protein, exhibiting high affinity with KDs of 0.004 nM, 0.041 nM, 0.019 nM, and 0.144 nM for KRAS wild type, G12D, G12C, and G12V variants, respectively, as determined by SPR binding assays. This compound demonstrates significant anti-proliferative activity, with IC50 values ranging from

    Out of stock

    All 3 sizes

Items 301-325 of 427

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