“pb 22”的搜索结果

产品 151 到 200 共 3389个

每页
页面:
  1. 2
  2. 3
  3. 4
  4. 5
  5. 6

设置降序顺序
  1. GDC046

    Catalog No. A22299
    Quick View
    TYK2 inhibitor
    GDC046 (Compound 3) is a potent, selective, and orally bioavailable inhibitor of TYK2 with Ki of 4.8 nM, 83.8 nM, 27.6 nM and 253 nM for TYK2, JAK1, JAK2, and JAK3, respectively. 了解更多
  2. BD750

    Catalog No. A22300
    Quick View
    JAK3/STAT5 inhibitor
    BD750, an effective immunosuppressant and a JAK3/STAT5 inhibitor, inhibits IL-2-induced JAK3/STAT5-dependent T cell proliferation, with IC50 values of 1.5 μM and 1.1 μM in mouse and human T cells, respectively. 了解更多
  3. BioE-1115

    Catalog No. A22301
    Quick View
    PASK inhibitor
    BioE-1115 is a highly selective and potent PAS kinase (PASK) inhibitor with an IC50 of ~4 nM. BioE-1115 is also a potent casein kinase 2α inhibitor with an IC50 of ~10 μM. 了解更多
  4. Homosalate

    Catalog No. A22302
    Quick View
    chemical UV filter
    Homosalate is an organic compound used in some sunscreens, it is used as a chemical UV filter, protecting the skin from sun damage. 了解更多
  5. Ribociclib hydrochloride

    Catalog No. A22303
    Quick View
    CDK4/6 inhibitor
    Ribociclib hydrochloride (LEE011 hydrochloride) is a highly specific CDK4/6 inhibitor with IC50 values of 10 nM and 39 nM, respectively, 了解更多
  6. Gallein

    Catalog No. A22304
    Quick View
    Gβγ subunit signalling inhibitor
    Gallein is a G protein βγ (Gβγ) subunit signalling inhibitor. Gallein disrupts the interaction of Gβγ subunits with the PI3Kγ. Anticancer agent. 了解更多
  7. SRX3207

    Catalog No. A22305
    Quick View
    Syk/PI3K inhibitor
    SRX3207 is an orally active and first-in-class dual Syk/PI3K inhibitor, with IC50 values of 10.7 nM and 861 nM for Syk and PI3Kα, respectively. SRX3207 relieves tumor immunosuppression. 了解更多
  8. BDTX-189

    Catalog No. A22306
    Quick View
    Anticancer agent
    BDTX-189 is a potent, orally active and selective inhibitor of allosteric EGFR and HER2 oncogenic mutations, including EGFR/HER2 exon 20 insertion mutants. BDTX-189 shows KDs of 0.2, 0.76, 13 and 1.2 nM for EGFR, HER2, BLK and RIPK2, reapectively. Anticancer activity. 了解更多
  9. LDN-193189 2HCl

    Catalog No. A22307
    Quick View
    BMP signaling inhibitor
    LDN193189 HCl (DM-3189) is the hydrochloride salt of LDN193189, which is a selective BMP signaling inhibitor, and inhibits the transcriptional activity of the BMP type I receptors ALK2 and ALK3 with IC50 of 5 nM and 30 nM in C2C12 cell lines, respectively, 200-fold selectivity for BMP versus TGF-β. 了解更多
  10. BpV(HOpic)

    Catalog No. A22308
    Quick View
    PTEN inhibitor
    BpV(HOpic) is a potent and selective inhibitor of PTEN with an IC50 of 14 nM. Nanocarrier-BpV(HOpic) has neuroprotective activity. 了解更多
  11. 2-Phospho-L-ascorbic acid trisodium

    Catalog No. A22309
    Quick View
    antioxidant
    2-Phospho-L-ascorbic acid trisodium acts as an antioxidant and a stimulator of hepatocyte growth factor (HGF) production. 了解更多
  12. Ferulic acid sodium

    Catalog No. A22310
    Quick View
    FGFR1 inhibitor
    Ferulic acid sodium is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC50s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively. 了解更多
  13. BL-918

    Catalog No. A22311
    Quick View
    ULK1 activator
    BL-918 is an orally active UNC-51-like kinase 1 (ULK1) activator with an EC50 of 24.14 nM. 了解更多
  14. L-Quebrachitol

    Catalog No. A22312
    Quick View
    natural product
    L-Quebrachitol is a natural product isolated from many plants, promotes osteoblastogenesis by uppregulation of BMP-2, runt-related transcription factor-2 (Runx2), MAPK (ERK, JNK, p38α), and Wnt/β-catenin signaling pathway. 了解更多
  15. Loureirin A

    Catalog No. A22313
    Quick View
    flavonoid
    Loureirin A is a flavonoid extracted from Dragon's Blood, can inhibit Akt phosphorylation, and has antiplatelet activity. 了解更多
  16. Kaempferol 3-neohesperidoside

    Catalog No. A22314
    Quick View
    flavonoid
    Kaempferol 3-neohesperidoside (Kaempferol 3-O-neohesperidoside) is a flavonoid. Kaempferol 3-neohesperidoside exhibits insulinomimetic effect on the rat soleus muscle. 了解更多
  17. Higenamine

    Catalog No. A22315
    Quick View
    β2-AR agonist
    Higenamine (Norcoclaurine), a β2-AR agonist, is a key component of the Chinese herb aconite root that prescribes for treating symptoms of heart failure in the oriental Asian countries. 了解更多
  18. Alflutinib

    Catalog No. A22316
    Quick View
    EGFR inhibitor
    Alflutinib is an EGFR inhibitor that targets both EGFR activating mutations and T790M, thus leading to tumor growth inhibition. 了解更多
  19. MCP110

    Catalog No. A22317
    Quick View
    inhibitor of Ras/Raf-1 interaction
    MCP110 is an inhibitor of Ras/Raf-1 interaction. MCP110 blocks the interaction of Ras with Raf. MCP110 disrupts this interaction might can be used for the research of human tumors. 了解更多
  20. BO-264

    Catalog No. A22318
    Quick View
    TACC3 inhibitor
    BO-264 is a highly potent and orally active transforming acidic coiled-coil 3 (TACC3) inhibitor with an IC50 of 188 nM and a Kd of 1.5 nM. 了解更多
  21. DCLK1-IN-1

    Catalog No. A22319
    Quick View
    chemical probe
    DCLK1-IN-1 is a selective, oral bioavailability in vivo-compatible chemical probe of the doublecortin like kinase 1 (DCLK1 kinase) domain. 了解更多
  22. IM156

    Catalog No. A22320
    Quick View
    AMPK activator
    IM156 (HL156A), a metformin derivative, is a potent activator of AMPK that increases AMPK phosphorylation. 了解更多
  23. ABTL-0812

    Catalog No. A22321
    Quick View
    antineoplastic agent
    ABTL-0812 (α-Hydroxylinoleic acid) induces endoplasmic reticulum (ER) stress-mediated autophagy. ABTL-0812 is a first-in-class small molecule with anti-cancer activity. 了解更多
  24. Remibrutinib

    Catalog No. A22322
    Quick View
    BTK inhibitor
    Remibrutinib, is a potent and orally active bruton tyrosine kinase (BTK) inhibitor with an IC50 value of 1 nM. 了解更多
  25. Benzamidine hydrochloride

    Catalog No. A22323
    Quick View
    trypsin-like serine proteases inhibitor
    Benzamidine hydrochloride is an reversible competitive inhibitor of trypsin-like serine proteases, with Kis of 97 ?M, 21 ?M, 20 ?M and 110 ?M for uPA, trypsin, tryptase and factor Xa, respectively. 了解更多
  26. AG1557

    Catalog No. A22324
    Quick View
    EGFR inhibitor
    AG1557 is a specific and ATP competitive inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase, has a pIC50 value of 8.194. 了解更多
  27. Ehp inhibitor 2

    Catalog No. A22325
    Quick View
    Eph family tyrosine kinase inhibitor
    Ehp inhibitor 2 is a Eph family tyrosine kinase inhibitor. 了解更多
  28. SU5204

    Catalog No. A22326
    Quick View
    tyrosine kinase inhibitor
    SU5204, a tyrosine kinase inhibitor, has IC50s of 4 and 51.5 μM for FLK-1 (VEGFR-2) and HER2, respectively. 了解更多
  29. SYN1143

    Catalog No. A22327
    Quick View
    dual c-Met/RON inhibitor
    SYN1143 is a potent, selective and orally active dual inhibitor of c-Met/RON, with IC50s of 4 and 9 nM, respectively. 了解更多
  30. RO495

    Catalog No. A22328
    Quick View
    Non-receptor TYK2 inhibitor
    RO495 (CS-2667) is a potent inhibitor of Non-receptor tyrosine-protein kinase 2 (TYK2). 了解更多
  31. S6K-18

    Catalog No. A22329
    Quick View
    ribosomal protein S6 kinase beta-1 inhibitor
    S6K-18 is a highly selective inhibitor of ribosomal protein S6 kinase beta-1 (S6K1, p70S6K, p70-S6K). 了解更多
  32. BAY-474

    Catalog No. A22330
    Quick View
    tyrosine-protein kinase c-Met inhibitor
    BAY-474 is a tyrosine-protein kinase c-Met inhibitor. BAY-474 acts as an epigenetics probe. 了解更多
  33. MAZ51

    Catalog No. A22331
    Quick View
    VEGFR-3 (Flt-4) tyrosine kinase inhibitor
    MAZ51 is a selective inhibitor of VEGFR-3 (Flt-4) tyrosine kinase. 了解更多
  34. BRD6989

    Catalog No. A22332
    Quick View
    inhibitor of CDK8 and CDK19
    BRD6989 is a selective inhibitor of CDK8 and CDK19. BRD6989 upregulates IL-10. BRD6989 is an analog of the natural product cortistatin A (dCA). 了解更多
  35. IRAK4-IN-4

    Catalog No. A22333
    Quick View
    IRAK4 inhibitor
    IRAK4-IN-4 is an interleukin-1 receptor-associated kinase 4 (IRAK4) inhibitor extracted from patent CN107163044A, Compound15, has an IC50 of 2.8 nM. 了解更多
  36. Mobocertinib

    Catalog No. A22334
    Quick View
    inhibitor of EGFR and HER2 oncogenic mutants
    Mobocertinib (TAK-788) is a potent and orally active inhibitor of EGFR and HER2 oncogenic mutants, including exon 20 insertions, with selectivity over WT EGFR. Antitumor activity. 了解更多
  37. TH-257

    Catalog No. A22335
    Quick View
    inhibitor of LIMK1 and LIMK2
    TH-257 is a potent inhibitor of LIMK1 and LIMK2 with IC50 values of 84 nM and 39 nM for LIMK1 and LIMK2, respectively, and it can be used as a chemical probe for LIMK1 and LIMK2. 了解更多
  38. BSJ-03-123

    Catalog No. A22336
    Quick View
    CDK6-selective small-molecule degrader
    BSJ-03-123 is a potent and novel CDK6-selective small-molecule degrader (PROTAC). 了解更多
  39. SR-4835

    Catalog No. A22337
    Quick View
    dual inhibitor of CDK12/CDK13
    SR-4835 is a potent, highly selective and ATP competitive dual inhibitor of CDK12/CDK13 (CDK12: IC50=99 nM, Kd=98 nM; CDK13: Kd=4.9 nM). 了解更多
  40. AS2863619

    Catalog No. A22338
    Quick View
    CDK8 and CDK19 inhibitor
    AS2863619 is a potent, orally active cyclin-dependent kinase 8 (CDK8) and CDK19 inhibitor with IC50s of 0.61 nM and 4.28 nM, respectively. 了解更多
  41. ASP4132

    Catalog No. A22339
    Quick View
    AMPK activator
    ASP4132 is an orally active, potent AMPK activator with an EC50 of 18 nM. ASP4132 has anti-cancer activity and makes tumor regression in breast cancer xenograft mouse models. 了解更多
  42. Decursinol angelate

    Catalog No. A22340
    Quick View
    cytotoxic and protein kinase C (PKC) activating agent
    Decursinol angelate, a cytotoxic and protein kinase C (PKC) activating agent from the root of Angelica gigas, possesses anti-tumor and anti-inflammatory activities. 了解更多
  43. 3'-Hydroxypterostilbene

    Catalog No. A22341
    Quick View
    natural pterostilbene analogue
    3'-Hydroxypterostilbene, a natural pterostilbene analogue, effectively inhibits the growth of human colon cancer cells (IC50s of 9.0, 40.2, and 70.9 ?M for COLO 205, HCT-116, and HT-29 cells, respectively) by inducing apoptosis and autophagy. 了解更多
  44. 7-Nitroindazole

    Catalog No. A22342
    Quick View
    neuronal nitric oxide synthase inhibitor
    7-Nitroindazole, a heterocyclic compound, acts as a selective inhibitor for neuronal nitric oxide synthase showing a 10-fold selectivity for neuronal NOS. 了解更多
  45. Chromium picolinate

    Catalog No. A22343
    Quick View
    nutritional supplement
    Chromium picolinate is a coordination complex consisting of chromium(III) and picolinic acid. It is used as a nutritional supplement for optimal insulin function in patients with Type 2 diabetes or promotion of weight loss. 了解更多
  46. Dihydrocaffeic acid

    Catalog No. A22344
    Quick View
    Antioxidant agent
    Dihydrocaffeic acid is a phenolic acid found in Gynura bicolor, reduces phosphorylation of MAPK p38 and prevent UVB-induced skin damage. Antioxidant potential and anti-inflammatory activity. 了解更多
  47. JNJ-38158471

    Catalog No. A22345
    Quick View
    VEGFR-2 inhibitor
    JNJ-38158471 is a well tolerated, orally available, highly selective VEGFR-2 inhibitor, with an IC50 of 40 nM. JNJ-38158471 also inhibits Ret and Kit with IC50s of 180 and 500 nM, respectively. 了解更多
  48. AUDA

    Catalog No. A22346
    Quick View
    sEH inhibitor
    AUDA (compound 43) is a potent soluble epoxide hydrolase (sEH) inhibitor with IC50s of 18 and 69 nM for the mouse and human sEH, respectively. AUDA has anti-inflammatory activity. 了解更多
  49. 3-Deazaadenosine hydrochloride

    Catalog No. A22347
    Quick View
    inhibitor of S-adenosylhomocysteine hydrolase
    3-Deazaadenosine (hydrochloride) is an inhibitor of S-adenosylhomocysteine hydrolase, with a Ki of 3.9 ?M; 3-Deazaadenosine has anti-inflammatory, anti-proliferative and anti-HIV activity. 了解更多
  50. CCG-222740

    Catalog No. A22348
    Quick View
    MRTF pathway inhibitor
    CCG-222740 is an orally active and selective Rho/myocardin-related transcription factor (MRTF) pathway inhibitor. CCG-222740 is also a potent inhibitor of alpha-smooth muscle actin protein expression. 了解更多

产品 151 到 200 共 3389个

每页
页面:
  1. 2
  2. 3
  3. 4
  4. 5
  5. 6

设置降序顺序
Rewards