Displaying drugs 151 - 175 of 407 in total
| Name | Weight | Structure | Desription | Categories |
|---|---|---|---|---|
| Laronidase | 69899.4 C3160H4848N898O881S12 |  | A form of recombinant human alpha-L-iduronidase used to treat Hurler and Hurler-Scheie forms of mucopolysaccharidosis, a genetic deficiency of alpha-L-iduronidase. | Enzymes / Glycoside Hydrolases / Hydrolytic Lysosomal Glycosaminoglycan-specific Enzyme / Iduronidase, antagonists & inhibitors |
| Human C1-esterase inhibitor | 68000.0 |  | A C1 inhibitor used to prevent angioedema attacks associated with hereditary angioedema. | Drugs Used in Hereditary Angioedema |
| Conestat alfa | 67000.0 |  | A recombinant C1INH used for the treatment of acute attacks of hereditary angioedema (HAE) due to C1 esterase inhibitor deficiency in adults. | Drugs Used in Hereditary Angioedema |
| Albumin human | 66472.2 C2936H4624N786O889S41 |  | A purified form of human serum albumin used to replace lost albumin in patients with hypoalbuminemia, to treat hypovolemia and ascites, and as a part of some diagnostic imaging kits. | Blood Substitutes and Plasma Protein Fractions |
| Olipudase alfa | 63590.933 C2900H4373N783O791S24 |  | A recombinant human acid sphingomyelinase used to treat Acid Sphingomyelinase Deficiency (ASMD) in children and adults. | Alimentary Tract and Metabolism / Amino Acids, Peptides, and Proteins / Enzyme Replacement Therapy / Enzymes / Enzymes and Coenzymes / Esterases / Hydrolases / Phosphoric Diester Hydrolases / Proteins / Recombinant Proteins |
| Moxetumomab pasudotox | 63500.0 C2804H4339N783O870S14 |  | A CD22-specific antibody conjugated to a truncated exotoxin used to treat relapsed or refractory hairy cell leukemia in patients who have already been treated with a purine nucleoside analog and one other treatment. | CD22 (Clusters of Differentiation 22) inhibitors |
| Velaglucerase alfa | 63000.0 C2532H3850N672O711S16 | | An enzyme replacement therapy used for the long-term treatment of for pediatric and adult patients with type 1 Gaucher disease. | Enzymes / Hydrolytic Lysosomal Glucocerebroside-specific Enzyme |
| Hyaluronidase (human recombinant) | 61000.0 | | An enzyme used to improve the absorption and dispersion of parenterally administered fluids, drugs, and contrast agents. | Glycoside Hydrolases |
| Peginterferon alfa-2a | 60000.0 |  | A modified form of recombinant human interferon used to stimulate the innate antiviral response in the treatment of hepatitis B and C viruses. | Antiviral Agents / Drug Carriers / Interferon alpha / Interferons |
| Ropeginterferon alfa-2b | 60000.0 C16H29N3O6(C2H4O)n(C2H4O)n |  | A mono-pegylated type I interferon used to treat polycythemia vera. | Interferons |
| Dulaglutide | 59669.81 C2646H4044N704O836S18 |  | A GLP-1 agonist used to manage type 2 diabetes mellitus. | Glucagon-like peptide-1 (GLP-1) analogues |
| Anistreplase | 59042.3 C2569H3928N746O781S40 |  | A form of recombinant human tissue plasminogen activator used in the emergency treatment of myocardial infarction and pulmonary emboli. | Enzymes |
| Coagulation factor X human | 59000.0 |  | A coagulation factor used to treat Factor X deficiency to control bleeding. | Blood Coagulation Factors / Enzyme Precursors / Factor X / Factor X, agonists |
| Alteplase | 59000.0 C2569H3928N746O781S40 |  | A recombinant form of human tissue plasminogen activator used in the emergency treatment of myocardial infarction, ischemic stroke, and pulmonary emboli. | Enzymes |
| Romiplostim | 59000.0 C2634H4086N722O790S18 | | A fusion protein thrombopoietin (TPO) peptide analog that increases platelet counts by binding to and activating the human TPO receptor. Used to treat thrombocytopenia associated with chronic immune thrombocytopenia (ITP). | Receptors, Thrombopoietin, agonists / Thrombopoietin Receptor Agonist |
| Tenecteplase | 58951.2 C2561H3919N747O781S40 |  | A modified form of recombinant human tissue plasminogen activator used in the emergency treatment of myocardial infarction and pulmonary emboli. | Enzymes |
| Tagraxofusp | 57695.0 C2553 H4026 N692 O798 S16 |  | A CD123-directed cytotoxin used to treat blastic plasmacytoid dendritic cell neoplasm. | CD123 Interaction / Cytotoxins |
| Denileukin diftitox | 57647.3 C2560H4042N678O799S17 |  | A recombinant cytotoxic protein based on a combination of diphtheria toxin fragments and interleukin-2 used to treat cutaneous T-cell lymphoma by targeting the interleukin-2 receptor. | Antineoplastic Agents |
| Pancrelipase amylase | 57086.0 |  | A lipase used to treat pancreatic exocrine insufficiency. | Amylases / Amylases, antagonists & inhibitors / Glycoside Hydrolases |
| Taliglucerase alfa | 56637.9397 C2580H3918N680O727S17 | | A hydrolytic lysosomal glucocerebroside specific enzyme, used for long term enzyme replacement therapy in patients with Type 1 Gaucher disease. | Enzyme Replacement Therapy / Enzymes / Gaucher Disease / Hydrolytic Lysosomal Glucocerebroside-specific Enzyme |
| Galsulfase | 56012.6 C2534H3851N691O719S16 |  | A recombinant human enzyme used as replacement enzyme therapy for the treatment of of adults and children with Mucopolysaccharidosis VI, a rare genetic disorder caused by a deficiency of a lysosomal enzyme. | Enzymes / Hydrolytic Lysosomal Glycosaminoglycan-specific Enzyme |
| Alglucerase | 55597.4 C2532H3854N672O711S16 |  | A form of recombinant beta-glucocerebrosidase enzyme used to replace the deficient endogenous enzyme in the treatment of Gaucher disease. | Enzymes |
| Imiglucerase | 55597.4 C2532H3854N672O711S16 |  | A form of recombinant human beta-glucocerebrosidase enzyme used to replace the deficient endogenous enzyme in the treatment of Gaucher disease. | Enzyme Replacement Therapy / Enzymes / Gaucher Disease / Hydrolytic Lysosomal Glucocerebroside-specific Enzyme |
| Drotrecogin alfa | 55000.0 C1786H2779N509O519S29 |  | A form of recombinant activated human protein C used to reduce mortality in patients with severe sepsis by inhibiting coagulation Factors V and VIII. | Enzymes |
| Sebelipase alfa | 55000.0 C1968H2945N507O551S15 | | A recombinant lysosomal acid lipase used to treat lysosomal acid lipase deficiency. | Cholesterol Ester Storage Disease, drug therapy / Enzymes / Hydrolytic Lysosomal Cholesteryl Ester-specific Enzyme / Hydrolytic Lysosomal Triacylglycerol-specific Enzyme / Wolman Disease, drug therapy |
Displaying drugs 151 - 175 of 407 in total