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  • T77860TCO-PEG4-VC-PAB-MMAE；化合物 TCO-PEG4-VC-PAB-MMAETCO-PEG4-VC-PAB-MMAE

    TCO-PEG4-VC-PAB-MMAE is an agent-linker conjugate utilized in antibody-drug conjugates (ADCs), comprising a cleavable linker (TCO-PEG4-VC-PA) and the potent tubulin inhibitor MMAE [1].

    价 格：￥电议型 号：T77860产 地：中国大陆

  • T7753Thalidomide-O-COOH；化合物Thalidomide-O-COOHinhibit|||Ligands for E3 Ligase|||TCE35031|||ThalidomideOCOO

    Thalidomide-O-COOH (Cereblon ligand 3) is the Thalidomide-based Cereblon ligand used in the recruitment of CRBN protein. It can be connected to the ligand for protein by a linker to form PROTACs.

    价 格：￥电议型 号：T7753产 地：中国大陆

  • T7677JNK Inhibitor VIII；化合物JNK Inhibitor VIIITCS JNK 6o；TCS JNK 6o

    JNK Inhibitor VIII (TCS JNK 6o) is an ATP-competitive selective inhibitor of c-Jun N-terminal kinase (JNK)(IC50 values of 45 nM and 160 nM for JNK-1 and -2, respectively).

    价 格：￥电议型 号：T7677产 地：中国大陆

  • T76692Mosunetuzumab；莫妥珠单抗BTCT-4465A；BTCT-4465A

    Mosunetuzumab (BCT-4465A) is a humanized antibody based on immunoglobulin G1 that targets CD20 (B cells) and CD3 (T cells). Mosunetuzumab redirects T cells to engage and eliminate malignant B cells and can be used to study relapsed or refractory (R/R) B-cell non-Hodgkin lymphoma (B-NHL) and refractory follicular lymphoma.

    价 格：￥电议型 号：T76692产 地：中国大陆

  • T76685Glofitamab；格菲妥单抗RO7082859|||RG 6026|||CD20-TCB；RO7082859|||RG 6026|||CD20-TCB

    Glofitamab (RO7082859) is a novel bivalent antibody directed against CD20-binding T cells.Glofitamab promotes T cell proliferation and activation and tumor cell killing by binding to CD20 on malignant cells.Glofitamab can be used for the palliation of relapsed or refractory B-cell lymphomas.

    价 格：￥电议型 号：T76685产 地：中国大陆

  • T76672Aprutumab阿普卢妥单抗FGFR-moAb|||FGFR2-TTC|||BAY 1179470

    Aprutumab (BAY 1179470) is a human FGFR2 monoclonal antibody with affinity to FGFR2 isoforms FGFR2-IIIB and FGFR2-IIIC. Aprutumab is commonly used to synthesize antibody-drug conjugates.

    价 格：￥电议型 号：T76672产 地：中国大陆

  • T76554FITC-LC-TAT (47-57)；化合物 FITC-LC-TAT (47-57)FITC-LC-TAT (47-57)

    FITC-LC-TAT (47-57) is a fluorescein isothiocyanate (FITC)-labeled trans-activator of transcription (TAT) peptide, which is recognized as a cell-penetrating peptide (CPP). This compound enhances the yield and solubility of heterologous proteins [1].

    价 格：￥电议型 号：T76554产 地：中国大陆

  • T76464FITC-β-Ala-Amyloid β-Protein (1-42) (ammonium)；化合物 FITC-β-Ala-Amyloid β-Protein (1-42) (ammonium)FIT

    FITC-β-Ala-Amyloid β-Protein (1-42) ammonium, a fluorescein isothiocyanate (FITC)-tagged monomer peptide of Aβ1-42, is instrumental in Alzheimer’s disease pathogenesis [1].

    价 格：￥电议型 号：T76464产 地：中国大陆

  • T76366CART (55-76), rat；化合物 CART (55-76), ratCART (55-76), rat

    CART (55-76), rat, a neuropeptide comprising residues 55-76 of the CART peptide and serving as the N-terminal fragments of CART (55-102), functions as a rat satiety factor. It demonstrates potent appetite-suppressing activity and has a close association with leptin and neuropeptide Y. Additionally, CART (55-76), rat is known to induce anxiety and stress-related behavior [1].

    价 格：￥电议型 号：T76366产 地：中国大陆

  • T76365CART (1-39), Human, Rat；化合物 CART (1-39), Human, RatCART (1-39), Human, Rat

    CART (1-39), Human, Rat is a neuropeptide comprising the first 39 residues of the CART peptide. This compound serves as a rat satiety factor, possessing significant appetite-suppressing effects, and demonstrates a close association with leptin and neuropeptide Y. It effectively inhibits regular and starvation-induced feeding and has the capacity to induce anxiety and stress-related behaviors [1].

    价 格：￥电议型 号：T76365产 地：中国大陆

  • T76327CTCE-0214；化合物 CTCE-0214CTCE-0214

    CTCE-0214, a chemokine CXC receptor 4 (CXCR4) agonist and SDF-1α (stromal cell-derived factor-1α) peptide analog, exhibits anti-inflammatory properties. It is applicable in the research of inflammation, sepsis, and systemic inflammatory syndromes [1] [2] [3].

    价 格：￥电议型 号：T76327产 地：中国大陆

  • T76065LOmiganan-FITC TFA；化合物 Omiganan-FITC TFAOmiganan-FITC TFA

    Omiganan-FITC TFA, a compound integrating the bactericidal and fungicidal cationic peptide Omiganan with a fluorescein isothiocyanate (FITC), is under development as a topical gel aimed at preventing catheter-associated infections [1].

    价 格：￥电议型 号：T76065L产 地：中国大陆

  • T76065Omiganan-FITC；化合物 Omiganan-FITCOmiganan-FITC

    Omiganan-FITC is a complex of the cationic peptide Omiganan, which possesses bactericidal and fungicidal properties and is under development as a topical gel for preventing catheter-associated infections, and Fluorescein Isothiocyanate (FITC), a fluorescein derivative used for amine labeling [1].

    价 格：￥电议型 号：T76065产 地：中国大陆

  • T75957Sphistin Synthetic Peptide(12-38,Fitc in N-Terminal-Fluorescently Labeled Peptide)；化合物 Sphistin Synt

    Sphistin Synthetic Peptide (12-38, Fitc in N-Terminal-Fluorescently Labeled Peptide) represents truncated fragments of the parent Sphistin Synthetic Peptide, characterized by the presence of a fluorescent label (Fitc) at the N-terminal.

    价 格：￥电议型 号：T75957产 地：中国大陆

  • T75874tcY-NH2 TFA；化合物 tcY-NH2 TFAtcY-NH2 TFA

    tcY-NH2 (trans-Cinnamoyl)-YPGKF-NH2) TFA is a selective PAR4 antagonist peptide with potent properties. It effectively inhibits thrombin- and AY-NH2-induced platelet aggregation and endostatin release. This compound finds utility in inflammation and immunology research [1] [2] [6].

    价 格：￥电议型 号：T75874产 地：中国大陆

  • T75802CTCE-9908 TFA；化合物 CTCE-9908 TFACTCE-9908 TFA

    CTCE-9908 TFA, a potent and selective CXCR4 antagonist, triggers mitotic catastrophe and cytotoxicity, and suppresses migration in ovarian cancer cells expressing CXCR4 [1] [2].

    价 格：￥电议型 号：T75802产 地：中国大陆

  • T75801TC14012 TFA；化合物 TC14012 TFATC14012 TFA

    TC14012 TFA, a serum-stable derivative of T140, is a selective peptidomimetic CXCR4 antagonist with an IC50 value of 19.3 nM. It also acts as a potent CXCR7 agonist, exhibiting an EC50 of 350 nM for recruiting β-arrestin 2 to CXCR7. This compound demonstrates anti-HIV and anti-cancer activities [1] [2].

    价 格：￥电议型 号：T75801产 地：中国大陆

  • T75614Kouitchenside G；化合物 Kouitchenside GKouitchenside G

    Kouitchenside G, a natural compound extracted from Swertia kouitchensis, demonstrates inhibitory activity against α-Glucosidase, showcasing an IC 50 value of 956 μM [1].

    价 格：￥电议型 号：T75614产 地：中国大陆

  • T75414alpha-1,4-Galactosyltransferase (LgtC)；化合物 alpha-1,4-Galactosyltransferase (LgtC)alpha-1,4-Galactosy

    Alpha-1,4-Galactosyltransferase (LgtC) (A4GALT), a glycosphingolipid-specific glycosyltransferase, catalyzes the transfer of a galactose molecule to the alpha-1,4 position on lactosylceramide, resulting in the formation of globotriaosylceramide. This enzyme plays a crucial role in the synthesis of P1 blood group antigens [1] [2].

    价 格：￥电议型 号：T75414产 地：中国大陆

  • T75388FITC-GW3965；化合物 FITC-GW3965FITC-GW3965

    FITC-GW3965, a fluorescence-labeled liver X receptor β (LXRβ) agonist, is derived from GW3965 by substituting its trifluoromethyl group with an amide linkage to FITC. This tracer facilitates the study of LXRβ function [1].

    价 格：￥电议型 号：T75388产 地：中国大陆

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