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Inflammation/Immunology

Chemical structure

Cat.No.

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CAS no.

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  • YN430219 (S,R,S)-AHPC-C6-NH2 ... 2360522-76-3

    (S,R,S)-AHPC-C6-NH2 hydrochloride (VH032-C6-NH2 hydrochloride) is a synthesizedE3 ligase lig and -linker conjugatethat incorporates the VH032 based VHL lig and and a linker used forAKTPROTAC degrader. (S,R...

  • YN290285 RBN012759 2360851-29-0

    RBN012759 is a potent and selective inhibitor of PARP14 with IC50 of <3 nM and 5 nM for human catalytic domain and mouse catalytic domain, respectively. RBN012759 contributes to anti-tumor immune response.

  • YN270060 GSK840 2361146-30-5

    GSK840 (GSK'840) is areceptor-interacting protein kinase 3 (RIP3 or RIPK3)inhibitor, which binds RIP3 kinase domain with an IC50 of 0.9nM, and inhibits kinase activity with an IC50 of 0.3nM.

  • YN410017 GSK8612 2361659-62-1

    GSK8612 is a highly potent and selective inhibitor for TBK1 (Tank-binding Kinase-1) with pKd of 8.0. Within 10-fold affinity with respect to TBK1, no off-targets of GSK8612 could be identified.

  • YN310189 M‑89 2363165-42-6

    M-89 is a highly potent and specificmenininhibitor, with aKdof 1.4nM for binding to menin. M-89 inhibits themenin-mixed lineage leukemia (Menin-MLL) protein-protein interaction and has potential to treat MLL leukemia.

  • YN330140 STING ligand-1 2365039-41-2

    STING lig and -1 is a leadSTINGlig and with an IC50 of 68nM for HAQ STING.

  • YN330214 Complement C5-IN-1 2365402-67-9

    Complement C5-IN-1 (Compound 7) is a small-molecule inhibitor of complement component 5 protein (C5). Complement C5-IN-1 interacts with C5 to prevent its cleavage by the C5 convertase and blocks zymosan-induced the membrane-at...

  • YN330219 G150 2369751-30-2

    G150 is a potent and highly selective human cyclic GMP-AMP synthase (h-cGAS) inhibitor with IC50 of 10.2 nM.

  • YN330241 SR-717 free acid 2375420-34-9

    SR-717 free acid is a non-nucleotideSTINGagonist with EC50s of 2.1μM and 2.2μM in ISG-THP1 (WT) and ISG-THP1 cGAS KO (cGAS KO) cell lines, respectively. SR-717 free acid is a stable cyclic guanosin...

  • YN330240 SR-717 2375421-09-1

    SR-717 is a non-nucleotideSTINGagonist with EC50s of 2.1μM and 2.2μM in ISG-THP1 (WT) and ISG-THP1 cGAS KO (cGAS KO) cell lines, respectively. SR-717 is a stable cyclic guanosine monophosphate-aden...

  • YN330106 Ac-FLTD-CMK 2376255-48-8

    Ac-FLTD-CMK, a gasdermin D (GSDMD)-derived inhibitor, is a specificinflammatory caspasesinhibitor. Ac-FLTD-CMK is effective againstcaspases-1(IC50 of 46.7nM),caspases-4(IC50 of 1.49μM),caspases-5(IC50 of 329nM...

  • YN371048 NPD-1335 2376326-31-5

    NPD1335 is aTrypanosoma brucei phosphodiesterase B1(TbrPDEB1) inhibitor with submicromolar activities againstT. bruceiparasites. NPD1335 displays a greatly improved cytotoxicity profile. NPD1335 increases intracellular cAM...

  • YN250389 ZL0580 2377151-10-3

    ZL0580, a structurally close analog of ZL0590, induces epigenetic suppression ofHIVvia selectively binding to BD1 domain ofBRD4. ZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongati...

  • YN330138 PF-06928215 2378173-15-8

    PF-06928215 is acGAS (cyclic GMP-AMP Synthase)inhibitor with an IC50 of 4.9 μΜ. PF-06928215 has a high binding affinity of 0.2μM (Kd).

  • YN440242 Src Inhibitor 3 2380027-49-4

    Src Inhibitor 3 is a potent, orally activec-terminal Src kinase (CSK)with IC50 values below 3nM and 4nM in CSK HTRF and Caliper assay, respectively. Src Inhibitor 3 shows the ability to increase T cell proliferation...

  • YN480998 NF-56-EJ40 2380230-73-7

    NF-56-EJ40 is a potent, high-affinity, and highly selectivehuman SUCNR1 (GPR91)antagonist with an IC50 of 25nM and a Ki of 33nM, and shows almost no activity towards ratSUCNR1. NF-56-EJ40 has high affinity fo...

  • YN330271 OP-5244 2381268-71-7

    OP-5244 is a potent and orally bioavailable inhibitor ofCD73, with an IC50 of 0.25nM. OP-5244 reverses immunosuppression through blocking of adenosine production, and has the potential for the cancer research.

  • YN270214 Bcl-2-IN-2 2383085-86-5

    Bcl-2-IN-2 is a potent and selectiveBcl-2inhibitor with an IC50 of 0.034nM and also inhibits Bcl-xL with an IC50 of 43nM, showing >1000-fold selectivity for Bcl-2 over Bcl-xL.

  • YN370484 cGAMP disodium 2407516-83-8

    cGAMP disodium (Cyclic GMP-AMP disodium) is the third cyclic dinucleotide (CDN) to be discovered in bacteria. cGAMP disodium is an effective adjuvant for sublingual vaccination capable of promoting broad immunity including...

  • YN480477 LDC7559 2407782-01-6

    LDC7559 is agasdermin D (GSDMD)inhibitor via blocking neutrophil extracellular trap (NET) in the late stages.

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