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Home >> Proteins

Proteins

Products for  Proteins

  1. Cat.No. Product Name Information
  2. GC48520 Betulonaldehyde

    (+)-Betulonal, Betulonic Aldehyde

     A pentacyclic triterpenoid Betulonaldehyde Chemical Structure
  3. GC60647 Bis(maltolato)oxovanadium(IV) Bis(maltolato)oxovanadium(IV) (BMOV) is a potent, reversible, competitive and orally active pan-PTP (protein tyrosine phosphatases) inhibitor. Bis(maltolato)oxovanadium(IV) Chemical Structure
  4. GC78874 BMMP BMMP is an anti- HIV-1 agent and hnRNP M modulator. BMMP Chemical Structure
  5. GC42951 BMP-22 BMP-22 is an inhibitor of autotaxin (IC50 = 170 nM). BMP-22 Chemical Structure
  6. GC72918 BN-82685

    IRC-083065

     BN-82685 is a a quinone-based CDC25 inhibitor with IC50 of 201 nM, 117 nM, 109 nM, 160 nM, 249 nM, for CDC25C, CDC25C-cat, CDC25A, CDC25B2, CDC25B3, respectively. BN-82685 Chemical Structure
  7. GC63788 BN82002 hydrochloride BN82002 hydrochloride is a potent, selective and irreversible inhibitor of CDC25 phosphatase family. BN82002 hydrochloride inhibits CDC25A, CDC25B2, CDC25B3, CDC25C CDC25A, and 25C-cat with IC50 values of 2.4, 3.9, 6.3, 5.4, and 4.6 ?M, respectively. BN82002 hydrochloride displays ~20-fold greater selectivity over CD45 tyrosine phosphatase. BN82002 hydrochloride Chemical Structure
  8. GC74517 Botensilimab

    AGEN 1181

     Botensilimab (AGEN 1181), a human anti-cytotoxic T-lymphocyte antigen 4 (CTLA-4) monoclonal antibody, is an innate and adaptive immune activator. Botensilimab Chemical Structure
  9. GC74024 BPU BPU arrests cell cycle progression in the sub-G1 phase. BPU Chemical Structure
  10. GC42969 bpV(phen) (potassium hydrate)

    Bisperoxovanadium(phen), Potassium Bisperoxo(1,10phenanthroline) oxovanadate (V)

     bpV(phen) (potassium hydrate), a insulin-mimetic agent, is a potent protein tyrosine phosphatase (PTP) and PTEN inhibitor with IC50s of 38 nM, 343 nM and 920 nM for PTEN, PTP-β and PTP-1B, respectively. bpV(phen) (potassium hydrate) Chemical Structure
  11. GC42975 BRD32048 ETS variant 1 (ETV1) is a transcription factor oncogene implicated in several cancers where it has been altered by chromosomal translocation, gene amplification, or lineage dysregulation. BRD32048 Chemical Structure
  12. GC68296 Brentuximab vedotin Brentuximab vedotin Chemical Structure
  13. GC40824 Brevicompanine B Brevicompanine B is a fungal metabolite originally isolated from P. Brevicompanine B Chemical Structure
  14. GC46106 Butyrolactone V A fungal metabolite Butyrolactone V Chemical Structure
  15. GC48433 BX-320 An inhibitor of PDK1 BX-320 Chemical Structure
  16. GC43042 C17 Lactosylceramide (d18:1/17:0)

    N-Heptadecanoyl Lactosylceramide, LacCer(d18:1/17:0), Lactosylceramide (d18:1/17:0)

     C17 Lactosylceramide is a naturally occurring sphingolipid that has been found in human brain metastases of lung adenocarcinomas but not in healthy brain tissue. C17 Lactosylceramide (d18:1/17:0) Chemical Structure
  17. GC74464 Cadonilimab

    AK104

     Cadonilimab (AK104) is a humanized tetravalent IgG1 bispecific antibody targeting PD1/CTLA4. Cadonilimab Chemical Structure
  18. GC43126 Calcitonin (human) (trifluoroacetate salt)

    Ba 47175, Calcitonin (1-32) (human), hCT, Thyrocalcitonin (human)

     Calcitonin is a peptide hormone that lowers blood calcium levels and inhibits bone resorption. Calcitonin (human) (trifluoroacetate salt) Chemical Structure
  19. GC64161 Calcium glycerophosphate Calcium glycerophosphate is an inhibitor of intestinal alkaline phosphatase F3. Calcium glycerophosphate Chemical Structure
  20. GC74519 Cantuzumab ravtansine

    IMGN242; huC242-DM4

     Cantuzumab ravtansine (IMGN242; huC242-DM4), an ADC, is a humanized monoclonal antibody, huC242, covalently linked via a disulfide bond to DM4 (DM4 ). Cantuzumab ravtansine Chemical Structure
  21. GC48893 Carbazomycin B A bacterial metabolite with diverse biological activities Carbazomycin B Chemical Structure
  22. GC48850 Carbazomycin C A bacterial metabolite with diverse biological activities Carbazomycin C Chemical Structure
  23. GC79138 CAST-calpain-2 stabilizer-1 CAST-calpain-2 stabilizer-1 is a blood-brain barrier permeable stabilizer of CAST-calpain-2 interaction. CAST-calpain-2 stabilizer-1 Chemical Structure
  24. GC26578 Cathepsin L from human liver

    The cathepsin L (CTSL) gene is mapped to human chromosome 9q21.33.CAS Number: 60616-82-2

     Cathepsin L from human liver Chemical Structure
  25. GC74531 Catumaxomab Catumaxomab, a trifunctional IgG2 antibody, is composed of mouse and rat heavy and light chains and binds to human EpCAM and human CD 3 receptors. Catumaxomab Chemical Structure
  26. GC45403 CAY10735   CAY10735 Chemical Structure
  27. GC47062 CAY10766 An antiviral compound CAY10766 Chemical Structure
  28. GC79302 CCKBR agonist-1 CCKBR agonist-1 (Compound 3r1) is a Gq-protein-preferring cholecystokinin B receptor ( CCKBR ) agonist with an EC 50 of 35 pM. CCKBR agonist-1 Chemical Structure
  29. GC64948 CD38 inhibitor 1

    CD38-IN-78c, CD38 Inhibitor 78c

     CD38 inhibitor 1 is a potent CD38 inhibitor with an IC50 value of 1.9nM for mouse CD38. CD38 inhibitor 1 Chemical Structure
  30. GC62892 CDC25B-IN-2 CDC25B-IN-2 is a potent cdc25B inhibitor. CDC25B-IN-2 Chemical Structure
  31. GC79124 CDH11-IN-1 CDH11-IN-1 is a CDH11 inhibitor. CDH11-IN-1 Chemical Structure
  32. GC20109 Cefotiam hexetil hydrochloride

    CTM-HE hydrochloride; SCE-2174 hydrochloride

    Cefotiam hexetil hydrochloride (CTM-HE) is an oral third-generation cephalosporin, which is a prodrug of cefotiam, but has no anti-bacterial property. Cefotiam is an antibiotic.

     Cefotiam hexetil hydrochloride Chemical Structure
  33. GC15892 Cetrimonium Bromide (CTAB)

    Cetyltrimethyl Ammonium Bromide (CTAB)

     Cetrimonium Bromide (CTAB), a common used surfactant, act as a drug solubilizer with intrinsic antibacterial properties. Cetrimonium Bromide (CTAB) Chemical Structure
  34. GC68858 Cevostamab

    BFCR 4350A; RG 6160; RO 7187797

    Cevostamab (BFCR4350A; RG6160; RO7187797) is a humanized, IgG1-based bispecific antibody that targets the near-membrane extracellular domain of FcRH5 on multiple myeloma (MM) cells and CD3 on T cells. Additionally, Cevostamab promotes effective synapse formation, enhancing T cell killing activity against MM tumor cells.

     Cevostamab Chemical Structure
  35. GC52081 Chamazulene

    Dimethulene

    Chamazulene is a terpene that has been found in chamomile (M. recutita) flowers and has anti-inflammatory and antioxidant activities.

     Chamazulene Chemical Structure
  36. GC45885 Chloroquine-d5 (phosphate)

    DL-Chloroquine-d5

     An internal standard for the quantification of chloroquine Chloroquine-d5 (phosphate) Chemical Structure
  37. GC60706 Chrysophanol triglucoside Chrysophanol triglucoside is an anthraquinone isolated from Cassia obtusifolia, inhibits protein tyrosine phosphatases 1B (PTP1B) and α-glucosidase with IC50s of 80.17 and 197.06 ?M, respectively. Chrysophanol triglucoside Chemical Structure
  38. GC92120 CJC-1295 (acetate)

    Modified GRF (1-29); CJC-1295-no DAC; GHRH (1-29)-NH2

     CJC-1295 is a synthetic peptide derivative of growth hormone-releasing hormone (GHRH). CJC-1295 (acetate) Chemical Structure
  39. GC47098 CL2-SN-38 (dichloroacetic acid salt) An antibody-drug conjugate containing SN-38 CL2-SN-38 (dichloroacetic acid salt) Chemical Structure
  40. GC20061 ClAP (Alkaline Phosphatase, Calf intestinal)

    ClAP (Alkaline Phosphatase, Calf intestinal) is a membrane-bound glycoprotein that hydrolyzes a broad range of monophosphate esters at alkaline pH.

     ClAP (Alkaline Phosphatase, Calf intestinal) Chemical Structure
  41. GC49852 Clindamycin (hydrochloride hydrate) Clindamycin (hydrochloride hydrate) is a lincosamide antibiotic used to treat severe infections caused by susceptible anaerobes, streptococci, staphylococci, and pneumococci. Clindamycin primary clinical applications include osteomyelitis, respiratory tract infections, biliary tract infections, endocarditis, otitis media, skin and soft tissue infections, and sepsis. Clindamycin (hydrochloride hydrate) Chemical Structure
  42. GC43278 Clindamycin Sulfoxide

    U-25026A

     Clindamycin sulfoxide is an active metabolite of the antibiotic clindamycin. Clindamycin Sulfoxide Chemical Structure
  43. GC52171 Clindamycin-d3 (hydrochloride) Clindamycin-d3 (hydrochloride) is the deuterium labeled Clindamycin. Clindamycin-d3 (hydrochloride) Chemical Structure
  44. GC74600 Cofetuzumab pelidotin

    PF-06647020; ABBV-647; h6M24-vc0101

     Cofetuzumab pelidotin (PF-06647020) is a PTK7-targeting ADC comprising a humanized anti-PTK7 mAb joined to an auristatin microtubule inhibitor payload, auristatin-0101, by a cleavable valine-citrulline (vc)-based linker. Cofetuzumab pelidotin Chemical Structure
  45. GC20031 Collagen (Type I,From Bovine Achilles Tendon)

    Collagen is the most abundant protein in mammals, which plays an important role in the formation of tissues and organs, and is involved in various functional expressions of cells.This product is a collagen hydrolysate.

     Collagen (Type I,From Bovine Achilles Tendon) Chemical Structure
  46. GC27508 Collagenase (Type D, animal free)

    Collagenase (Type D, animal-free) does not contain animal-derived components and possesses collagenase and secondary protease activity similar to Type 1 and Type 2 collagenases.

     Collagenase (Type D, animal free) Chemical Structure
  47. GC26373 Collagenase D Collagenase D is an enzyme used to digest collagen and extracellular matrix (ECM). Collagenase D Chemical Structure
  48. GC19589 Collagenase I

    Collagenase; collagen hydrolase

     The collagenase currently has approximately four types: Type I collagenase, Type II collagenase, Type III collagenase, and Type IV collagenase, which have specific applications: Type I Collagenase: Contains a relatively uniform variety of enzyme activities (including collagenase, caseinase, clostripain, and trypsin activity). Collagenase I Chemical Structure
  49. GC19593 Collagenase IA

    Collagenase; collagen hydrolase

     Collagenase IA is a proteolytic enzyme commonly used to digest extracellular matrix proteins. Collagenase IA specifically acts on procollagen, breaking it and then hydrolyzing it with other proteases, but does not hydrolyze fibrin and globulin. Collagenase IA Chemical Structure
  50. GC19588 Collagenase II

    Collagenase; collagen hydrolase

     Collagenase Ⅱ is a matrix metalloproteinase (MMPs) used for tissue dissociation and the preparation of liver, bone, thyroid, heart, and salivary gland cells. Collagenase II Chemical Structure
  51. GC19590 Collagenase III

    Collagenase; collagen hydrolase

    Collagenase BR, IA type, >125CDU/mg

     Collagenase III Chemical Structure
  52. GC19591 Collagenase IV

    Collagenase; collagen hydrolase

    Collagenase IV, a member of the mammalian extracellular neutral metalloproteinases family, digests type IV collagen, a major component of the basement membrane derived from Bacillus histolyticus.

     Collagenase IV Chemical Structure
  53. GC19592 Collagenase V

    Collagenase; collagen hydrolase

     Collagenase V is a proteolytic enzyme that is commonly used to digest extracellular matrix proteins and is suitable for the separation of pancreatic islet cells and connective tissue cells. Collagenase V Chemical Structure
  54. GC26859 Collagenase, Type VII

    Type VII collagenase

     Collagenase, Type VII is a protein that catalyzes chemical processes and breaks the peptide bonds in collagen. Collagenase, Type VII Chemical Structure
  55. GC26774 Collagenase, Type VIII

    Collagenase, Type VIII is a mixed enzyme derived from Clostridium histolyticum that contains collagenase, a nonspecific protease, and a clostripain.

     Collagenase, Type VIII Chemical Structure
  56. GC47119 Colletodiol

    (+)-Colletodiol

     A fungal metabolite with immunosuppressive and antiviral activities Colletodiol Chemical Structure
  57. GC43310 Corticostatin (human) (trifluoroacetate salt)

    DEFA4 Protein, α-Defensin 4, Defensin HNP-4, Human Neutrophil Peptide 4, Neutrophil Defensin 4

     Corticostatin is a corticostatic peptide that has been found in human granulocytes. Corticostatin (human) (trifluoroacetate salt) Chemical Structure
  58. GC48954 CP21 An iron chelator CP21 Chemical Structure
  59. GC62909 CPT-157633 CPT-157633, a difluoro-phosphonomethyl phenylalanine derivative, and is a PTP1B inhibitor. CPT-157633 Chemical Structure
  60. GC92092 CTX-1211 (trifluoroacetate salt)

    Acetyl-Arg-cyclo(Cys-D-Ala-Arg-D-Phe-Arg-Trp-Cys)-NH2

     CTX-1211 is a peptide agonist of melanocortin receptors. CTX-1211 (trifluoroacetate salt) Chemical Structure
  61. GC43329 Cu-ATSM

    copper-ATSM, CuII(atsm)

     The metallo-protein Cu/Zn-superoxide dismutase (SOD1) is a ubiquitous enzyme responsible for scavenging superoxide radicals. Cu-ATSM Chemical Structure
  62. GC79043 Cusculine

    FAC21

     Cusculine (FAC21) is an oropouche virus (OROV) endonuclease inhibitor with an IC50 of 1.4 μM. Cusculine Chemical Structure
  63. GC68925 cyclo(RLsKDK) TFA

    BK-1361 TFA

    cyclo(RLsKDK) (TFA) (BK-1361 (TFA)) is a specific inhibitor of the metalloproteinase ADAM8, with an IC50 value of 182 nM. It has potential applications in inflammatory diseases and cancer.

     cyclo(RLsKDK) TFA Chemical Structure
  64. GC47139 Cycloaspeptide A A fungal metabolite Cycloaspeptide A Chemical Structure
  65. GC47142 Cycloguanil-d6 (hydrochloride)

    Chloroguanide Triazine-d6

     A neuropeptide with diverse biological activities Cycloguanil-d6 (hydrochloride) Chemical Structure
  66. GC43346 Cyclopamine-KAAD Cyclopamine-KAAD, a hedgehog signaling inhibitor, is a smoothened antagonist. Cyclopamine-KAAD Chemical Structure
  67. GC11328 Cyclosporine

    CsA; Cyclosporine A; Ciclosporin A

     Cyclosporine (cyclosporin A), a immunosuppressive agent, inhibits phosphatase activity of calcineurin with IC50 value of 5 nM . Cyclosporine Chemical Structure
  68. GC43360 Cytostatin Cytostatin is a natural antitumor inhibitor of cell adhesion to extracellular matrix, blocking adhesion of B16 melanoma cells to laminin and collagen type IV in vitro (IC50s = 1.3 and 1.4 μg/ml, respectively) and B16 cells metastatic activity in mice. Cytostatin Chemical Structure
  69. GC43361 Cytostatin (sodium salt) Cytostatin is a natural antitumor inhibitor of cell adhesion to extracellular matrix, blocking adhesion of B16 melanoma cells to laminin and collagen type IV in vitro (IC50s = 1.3 and 1.4 μg/ml, respectively) and B16 cells metastatic activity in mice. Cytostatin (sodium salt) Chemical Structure
  70. GC92128 Dapiglutide (sodium salt) Dapiglutide is a dual glucagon-like peptide 1 receptor (GLP-1R) and GLP-2R agonist. Dapiglutide (sodium salt) Chemical Structure
  71. GC19785 Daratumumab

    Daremuzumab; Anti-Human CD38, Human Antibody

     Daratumumab (DARA) is a human IgG1 mAb targeting CD38, a 46-kDa type II transmembrane glycoprotein that is expressed at high levels on malignant cells in multiple myeloma (MM). Daratumumab Chemical Structure
  72. GC73079 Datopotamab deruxtecan

    DS-1062; Dato-DXd

    Datopotamab deruxtecan is a TROP2-targeting antibody-drug conjugate (KD=0.74nM).

     Datopotamab deruxtecan Chemical Structure
  73. GC52191 Deacetylanisomycin

    (-)-Deacetylanisomycin, SA 3097D1

     Deacetylanisomycin is a potent growth regulator in plants and an inactive derivative of Anisomycin. Deacetylanisomycin Chemical Structure
  74. GC41151 Decursinol angelate Decursinol angelate is a pyranocoumarin that has been found in the Korean medicinal herb A. Decursinol angelate Chemical Structure
  75. GC18869 Deoxyenterocin

    5-Deoxyenterocin

     Deoxyenterocin is a bacterial metabolite originally isolated from Streptomyces that has diverse biological activities, including antibiotic, antiviral, and antioxidant properties. Deoxyenterocin Chemical Structure
  76. GC73019 Depatuxizumab mafodotin

    ABT-414

     Depatuxizumab mafodotin is an antibody-drug conjugate (ADC) that specifically targets the epidermal growth factor receptor (EGFR). Depatuxizumab mafodotin Chemical Structure
  77. GC73689 Depatuxizumab MMAE Depatuxizumab MMAE is an antibody-drug conjugate (ADC) comprising an anti EGFR monoclonal antibody (Depatuxizumab) and the cytotoxic agent Monometl auristatin E (MMAE). Depatuxizumab MMAE Chemical Structure
  78. GC47193 Desethyl Hydroxychloroquine-d4

    Cletoquine-d4, (±)-Desethylhydroxychloroquine-d4, DHCQ-d4

     An internal standard for the quantification of desethyl hydroxychloroquine Desethyl Hydroxychloroquine-d4 Chemical Structure
  79. GC47195 Desethylchloroquine-d4

    N-Desethylchloroquine-d4

     An internal standard for the quantification of desethylchloroquine Desethylchloroquine-d4 Chemical Structure
  80. GC49459 Desmopressin (trifluoroacetate salt)

    Adiuretin, DDAVP

     A vasopressin receptor agonist Desmopressin (trifluoroacetate salt) Chemical Structure
  81. GC43436 Diacetylcercosporin Diacetylcercosporin is a perylenequinone produced by Cercospora and Septoria that has diverse biological activities. Diacetylcercosporin Chemical Structure
  82. GC45992 Diallyl Tetrasulfide

    ICD-1585

     An organosulfur compound with diverse biological activities Diallyl Tetrasulfide Chemical Structure
  83. GC49153 Didemnin B

    NSC 325319, NSC 333841

     Didemnin B is a cyclic depsipeptide marine natural product with cytotoxicity. Didemnin B Chemical Structure
  84. GC43448 Didymin Didymin is a flavonoid that has been found in citrus fruits with diverse biological activities. Didymin Chemical Structure
  85. GC43451 Dieosinediglutathione

    DiEGSSG

     Dieosinediglutathione is the product of glutathione disulfide and eosin isothiocyanate which has been purified and lyophilized. Dieosinediglutathione Chemical Structure
  86. GC40751 Dihydroartemisinic Acid Dihydroartemisinic acid is a biosynthetic precursor to the antimalarial agent artemisinin and an intermediate in the synthesis of artemisinin from artemisinic acid . Dihydroartemisinic Acid Chemical Structure
  87. GC64039 Disitamab vedotin Disitamab vedotin is an antibody-drug conjugate (ADC) targeting HER2 protein that is comprised of hertuzumab coupling monomethyl auristatin E (MMAE) via a cleavable linker. Disitamab vedotin Chemical Structure
  88. GC39295 DJ001 DJ001 is a highly specific, selective and non-competitive protein tyrosine phosphatase-σ (PTPσ) inhibitor with an IC50 of 1.43 μM. DJ001 Chemical Structure
  89. GC90598 DOG-IM4

    An ionizable cationic lipid

     DOG-IM4 Chemical Structure
  90. GC45767 Dovitinib-d8 An internal standard for the quantification of dovitinib Dovitinib-d8 Chemical Structure
  91. GC45440 Doxycycline-d3 (hyclate)

     An internal standard for quantifying doxycycline

     Doxycycline-d3 (hyclate) Chemical Structure
  92. GC62943 DPM-1001 trihydrochloride DPM-1001 trihydrochloride is a potent, specific, orally active and non-competitive inhibitor of protein-tyrosine phosphatase (PTP1B) with an IC50 of 100 nM. DPM-1001 trihydrochloride Chemical Structure
  93. GP21570 DPP4 Protein Human Dipeptidyl Peptidase-IV DPP4 Protein Chemical Structure
  94. GC45442 DSPE-MPEG(2000) (sodium salt)

    1,2-Distearoyl-rac-glycero-3-PE-N-Polyethyleneglycol-2000, 1,2-Distearoyl-rac-glycerol-3-Phosphatidylethanolamine-N-Polyethyleneglycol-2000, 1,2-Distearoyl-rac-glycerol-3-Phosphoethanolamine-N-Polyethyleneglycol-2000, 1,2-DSPE-MPEG(2000)

       DSPE-MPEG(2000) (sodium salt) Chemical Structure
  95. GC91229 DXR Inhibitor 11a (free acid)

    An inhibitor of P. falciparum DXR

     DXR Inhibitor 11a (free acid) Chemical Structure
  96. GC91141 DXR Inhibitor 11a (sodium salt)

    An inhibitor of P. falciparum DXR

     DXR Inhibitor 11a (sodium salt) Chemical Structure
  97. GC73003 EBNA1-IN-SC7 EBNA1-IN-SC7 (compound SC7) is a selective Epstein-Barr nuclear antigen 1 (EBNA1) inhibitor that interferes with EBNA1-DNA binding activity with an IC50 value of 23 μM. EBNA1-IN-SC7 Chemical Structure
  98. GC73260 EBV lytic cycle inducer-1 Epstein-Barr virus (EBV) lytic cycle inducer-1 Dp44mT (compound C7) is an iron-chelatoe-like compound. EBV lytic cycle inducer-1 Chemical Structure
  99. GC72812 Ecallantide TFA

    DX-88 TFA

     Ecallantide (DX-88) TFA is a specific recombinant plasma kallikrein inhibitor. Ecallantide TFA Chemical Structure
  100. GC65260 EDP-305 EDP-305 is an orally active, potent and selective farnesoid X receptor (FXR) agonist, with EC50 values of 34 nM (chimeric FXR in CHO cells) and 8 nM (full-length FXR in HEK cells). EDP-305 Chemical Structure
  101. GC74613 Eftilagimod alfa

    IMP321; LAG-3Ig

     Eftilagimod alfa (IMP321) is a recombinant LAG-3Ig fusion protein that binds to MHC class II. Eftilagimod alfa Chemical Structure

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