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Ras

Ras

Le proteine Ras sono piccole GTPasi che agiscono come interruttori molecolari nella via di segnalazione MAPK, controllando la crescita, la differenziazione e la sopravvivenza cellulare. Ras attivato avvia una cascata di segnalazione che include Raf, MEK ed ERK, portando a varie risposte cellulari. Le mutazioni nei geni Ras sono comuni nei tumori, rendendo Ras un importante focus della ricerca sul cancro. Presso CymitQuimica, offriamo una gamma di modulatori di Ras per supportare la tua ricerca in biologia del cancro, trasduzione del segnale e sviluppo terapeutico.

Trovati 167 prodotti per "Ras".

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  • pan-KRAS-IN-4

    CAS:
    Pan-KRAS-IN-4 (compound 5) is a potent KRAS inhibitor, demonstrating IC50 values of 0.37 nM for Kras G12C and 0.19 nM for Kras G12V [1].
    Formula:C36H34F2N6O3
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:636.69

    Ref: TM-T79799

    25mg
    1.908,00€
    50mg
    2.502,00€
    100mg
    3.330,00€
  • J-104871

    CAS:
    J-104871 (UNII-6137X5QNJF) is an FTase inhibitor that inhibits tumor growth in nude mice transplanted with activated H-ras-transformed NIH3T3 cells.
    Formula:C38H32N2O12
    Purezza:99.03%
    Colore e forma:Solid
    Peso molecolare:708.67

    Ref: TM-T24188

    1mg
    109,00€
    5mg
    261,00€
    10mg
    374,00€
    25mg
    583,00€
  • KRAS inhibitor-35

    CAS:
    KRAS inhibitor-35 (compound 72) is a KRAS inhibitor with an IC50 of 2 nM, utilized in tumor research.
    Formula:C38H32F4N6O3S
    Colore e forma:Solid
    Peso molecolare:728.76

    Ref: TM-T200557

    25mg
    2.583,00€
    50mg
    3.402,00€
    100mg
    4.680,00€
  • KRAS inhibitor-37

    CAS:
    KRAS inhibitor-37 (compound 2) is a potent inhibitor of KRAS, exhibiting low dissociation constants (KD) with various KRAS mutations: wild type (0.004 nM), G12D (0.041 nM), G12C (0.019 nM), and G12V (0.144 nM). This compound effectively inhibits cell proliferation, demonstrating half-maximal inhibitory concentrations (IC50) ranging from <2 nM to 14 nM in H358, SW620, and PANC08.13 cell lines. KRAS inhibitor-37 holds potential for cancer research applications.
    Formula:C32H33ClFN7O3
    Colore e forma:Solid
    Peso molecolare:618.10

    Ref: TM-T201259

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  • Pan-RAS-IN-7

    CAS:
    Pan-RAS-IN-7 (Compound D101) is a broad-spectrum RAS inhibitor used in the synthesis of antibody-drug conjugates (ADCs). It is also applicable in cancer research.
    Formula:C59H76N8O8
    Colore e forma:Solid
    Peso molecolare:1025.28

    Ref: TM-T201152

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  • KRAS inhibitor-34

    CAS:
    KRAS inhibitor-34 (compound 27) is a KRAS inhibitor with an IC50 of 6.4 nM and is utilized in oncological research.
    Formula:C43H41F3N6O3
    Colore e forma:Solid
    Peso molecolare:746.82

    Ref: TM-T200670

    25mg
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  • SOF-436

    CAS:
    SOF-436 is a KRAS inhibitor that can suppress SOS1-mediated KRAS nucleotide exchange (IC50 = 60 μM) and inhibit the interaction between KRAS and the effector protein RAF. SOF-436 is applicable to cancer research.
    Formula:C15H13F2NO4S2
    Colore e forma:Solid
    Peso molecolare:373.395

    Ref: TM-T206673

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  • KRAS inhibitor-32

    CAS:
    KRAS inhibitor-32 (compound 139A) is a KRAS inhibitor utilized in cancer research.
    Formula:C29H35FN10OS2
    Colore e forma:Solid
    Peso molecolare:622.78

    Ref: TM-T200688

    25mg
    3.348,00€
    50mg
    4.213,00€
    100mg
    5.580,00€
  • KRASG12D-IN-5

    CAS:
    KRASG12D-IN-5 (Compound 241) is an orally active KRAS(G12D) inhibitor with an IC50 of 11 nM. It demonstrates potent anticancer activity without significant cytotoxicity to BxPC-3 cells (wild-type), KRAS-mutant AsPC-1 cells (G12D), and MIAPaCa-2 cells (G12C), with CC50 values of 10.37, 0.76, and 0.3 μM, respectively. KRASG12D-IN-5 is applicable in cancer studies, including lung, pancreatic, and colorectal cancers.
    Formula:C34H31F5N6O2
    Colore e forma:Solid
    Peso molecolare:650.64

    Ref: TM-T211223

    10mg
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  • KRAS-IN-5

    CAS:
    KRAS-IN-5 (Compound Ex 6) is an orally active, selective inhibitor that targets KRAS mutants, including KRASG12D, KRASG12V, and KRASWT, with an impressive GNE IC50 value of 1.3 nM for KRASG12D. By inhibiting KRAS-mediated signaling pathways, such as reducing ERK phosphorylation, KRAS-IN-5 effectively prevents tumor cell proliferation. This compound holds potential for research into cancers associated with KRAS mutations, such as pancreatic cancer, colorectal cancer, and lung cancer.
    Formula:C35H36F3N7O3
    Colore e forma:Solid
    Peso molecolare:659.70

    Ref: TM-T211066

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  • RGT-018

    CAS:
    RGT-018 is a potent oral SOS1 inhibitor with antitumor properties. It exerts its anticancer activity by inhibiting KRAS activation, thereby hindering cancer cell proliferation.
    Formula:C27H24F3N7O2
    Colore e forma:Solid
    Peso molecolare:535.52

    Ref: TM-T89897

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  • KRASG12C IN-18

    CAS:
    KRASG12C IN-18 is an orally active covalent inhibitor of KRASG12C, achieving complete covalent binding to KRASG12C in both GDP- and GMPPNP-bound states. It exhibits significant antiproliferative activity against KRASG12C and its resistant mutations (including KRASG12C/R68S) with an IC50 in the low nanomolar range. KRASG12C IN-18 demonstrates notable in vivo efficacy in KRASG12C-driven solid tumors and KRASG12C/R68S xenograft models, making it applicable for colorectal adenocarcinoma research.
    Formula:C37H32F4N6O2
    Peso molecolare:668.7

    Ref: TM-T214145

    10mg
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  • KRAS inhibitor-31

    CAS:
    KRAS inhibitor-31 (compound 33), a potent agent targeting KRAS, exhibits K D (SPR) values of 0.019 nM for KRas G12D, 0.019 nM for KRas G12C, and 0.096 nM for KRas G12V, illustrating its efficacy across these variants.
    Formula:C33H30F3N5O4
    Colore e forma:Solid
    Peso molecolare:617.62

    Ref: TM-T200064

    25mg
    3.943,00€
    50mg
    5.211,00€
    100mg
    6.759,00€
  • Sosimerasib

    CAS:
    Sosimerasib is an inhibitor of the kirsten rat sarcoma viral oncogene homolog (KRAS) and exhibits antitumor activity.
    Formula:C36H39ClFN7O4
    Colore e forma:Solid
    Peso molecolare:688.191

    Ref: TM-T206171

    10mg
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  • KRAS inhibitor-41

    CAS:
    KRAS inhibitor-41 is a KRAS inhibitor with an IC50 value of less than 0.01 μM for both KRAS G12D and KRAS G12V mutations. It effectively inhibits RAS mutant cell lines GP2D (KRAS-G12D) and SW620 (KRAS-G12V). KRAS inhibitor-41 is applicable for cancer research.
    Formula:C30H37FN10OS
    Colore e forma:Solid
    Peso molecolare:604.745

    Ref: TM-T206791

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  • KRAS G12D inhibitor 28

    CAS:
    KRAS G12D inhibitor 28 (Compound 1) is an inhibitor of KRAS G12D and can be utilized in cancer research.
    Formula:C35H32Cl2FN5O
    Colore e forma:Solid
    Peso molecolare:628.57

    Ref: TM-T207473

    10mg
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  • (+)-Perillyl alcohol

    CAS:
    (+)-Perillyl alcohol (0.25-1 mM) inhibits cell growth in SW480 cells. At a concentration of 1 mM and a duration of 24 hours, (+)-Perillyl alcohol increases the number of cells in the G0/G1 phase and reduces the number in the S phase in SW480 cells.
    Formula:C10H16O
    Colore e forma:Solid
    Peso molecolare:152.23

    Ref: TM-T88792

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  • PAT-IN-1

    CAS:
    PAT-IN-1, a protein acyl transferases (PAT) inhibitor, competitively inhibits Erf2 autopalmitoylation (WO2017011518A1; compound 13) [1].
    Formula:C45H68N4O
    Colore e forma:Solid
    Peso molecolare:681.05

    Ref: TM-T87110

    10mg
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  • KRAS G12C inhibitor 15

    CAS:
    KRAS G12C inhibitor 15 is a potent KRAS G12C inhibitor .
    Formula:C25H21ClF2N4O3
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:498.91

    Ref: TM-T11769

    25mg
    1.908,00€
    50mg
    2.502,00€
    100mg
    3.330,00€
  • KRAS inhibitor-8

    CAS:
    KRAS inhibitor-8 is a potent KRAS G12C inhibitor.
    Formula:C26H24ClF4N5O3
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:565.95

    Ref: TM-T11775

    25mg
    2.313,00€
    50mg
    3.042,00€
    100mg
    4.140,00€