Category: 216959-94-3

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 216959-94-3, Name is 4-(2-Amino-4-thiazolyl)benzoic Acid, molecular formula is C10H8N2O2S. In a Patent，once mentioned of 216959-94-3, HPLC of Formula: C10H8N2O2S

Disclosed are compounds having Formula (I) and the compositions and methods thereof for treating or preventing a viral infection mediated at least in part by a virus in the Flaviviridae family of viruses, wherein A, R2, m, R, V, W, T, Z, R1, Y, and p are disclosed herein.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.HPLC of Formula: C10H8N2O2S. In my other articles, you can also check out more blogs about 216959-94-3

Reference：
Thiazole | C3H4570NS – PubChem,
Thiazole | chemical compound | Britannica

216959-94-3, Name is 4-(2-Amino-4-thiazolyl)benzoic Acid, molecular formula is C10H8N2O2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 216959-94-3, name: 4-(2-Amino-4-thiazolyl)benzoic Acid

Disclosed are compounds, stereoisomers, tautomers, pharmaceutically acceptable salts, or prodrugs thereof of having Formula (I), their preparation, use, and compositions thereof for treating an infection mediated at least in part by a virus in the Flaviviridae family of viruses, wherein A, R3, X, V, W, T, Z, R, Y1, and p are as defined herein.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.name: 4-(2-Amino-4-thiazolyl)benzoic Acid. In my other articles, you can also check out more blogs about 216959-94-3

Reference：
Thiazole | C3H4568NS – PubChem,
Thiazole | chemical compound | Britannica

216959-94-3, Name is 4-(2-Amino-4-thiazolyl)benzoic Acid, molecular formula is C10H8N2O2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 216959-94-3, SDS of cas: 216959-94-3

Disclosed are compounds, stereoisomers, tautomers, pharmaceutically acceptable salts, or prodrugs thereof of having Formula (I), their preparation, use, and compositions thereof for treating an infection mediated at least in part by a virus in the Flaviviridae family of viruses, wherein A, L1, V, W, T, Z, R, Y1, and p are as defined herein.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.SDS of cas: 216959-94-3. In my other articles, you can also check out more blogs about 216959-94-3

Reference：
Thiazole | C3H4569NS – PubChem,
Thiazole | chemical compound | Britannica

Electric Literature of 216959-94-3. Let¡¯s face it, organic chemistry can seem difficult to learn. Especially from a beginner¡¯s point of view. Like 216959-94-3, Name is 4-(2-Amino-4-thiazolyl)benzoic Acid. In a document type is Patent, introducing its new discovery.

Sulfonyl derivatives represented by general formula (I), salts of the same, and solvates of both: and application of them as drugs: [wherein R1 is hydrogen, hydroxyl, nitro or the like; R2 and R3 are each independently hydrogen, halogeno or the like; R4 and R5 are each dependently hydrogen, halogeno or the like; Q1 is an optionally substituted saturated or unsaturated 5- or 6-membered cyclic hydrocarbon group or the like; Q2 is a single bond, oxygen or the like; Q3 is, e.g., a group represented by formula (a): T1 is carbonyl or the like; and X1 and X2 are each independently methylidyne or nitrogen]. These compounds exhibit potent Fxa inhibiting activities and serve as excellent anticoagulants which speedily exert satisfactory and persistent anti-thrombotic effects through oral administration and little cause adverse effects.

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Reference£º
Thiazole | C3H4566NS – PubChem,
Thiazole | chemical compound | Britannica

Related Products of 216959-94-3, An article , which mentions 216959-94-3, molecular formula is C10H8N2O2S. The compound – 4-(2-Amino-4-thiazolyl)benzoic Acid played an important role in people’s production and life.

Small molecule inhibitors of the HIV-1 nucleocapsid protein (NC) are considered as promising agents in the treatment of HIV/AIDS. In an effort to exploit the privileged 2-amino-4-phenylthiazole moiety in NC inhibition, here we conceived, synthesized, and tested in vitro 18 NC inhibitors (NCIs) bearing a double functionalization. In these NCIs, one part of the molecule is deputed to interact noncovalently with the NC hydrophobic pocket, while the second portion is designed to interact with the N-terminal domain of NC. This binding hypothesis was verified by molecular dynamics simulations, while the linkage between these two pharmacophores was found to enhance antiretroviral activity both on the wild-type virus and on HIV-1 strains with resistance to currently licensed drugs. The two most interesting compounds 6 and 13 showed no cytotoxicity, thus becoming valuable leads for further investigations.

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Reference£º
Thiazole | C3H4567NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 216959-94-3, Name is 4-(2-Amino-4-thiazolyl)benzoic Acid, molecular formula is C10H8N2O2S. In a Patent£¬once mentioned of 216959-94-3, Recommanded Product: 216959-94-3

A compound represented by the following formula (1):Q1-Q2-To-N(R1)-Q3-N(R2)-T1-Q4 [wherein, R¹ and R² are hydrogen atoms or the like; Q¹ is a saturated or unsaturated, 5- or 6- membered cyclic hydrocarbon group which may have a substituent, or the like; Q² is a single bond or the like; Q³ represents the following group: -C(R^3a)(R^4a)-{C(R^3b)(R^4b)}m¹-{C(R^3c)(R^4c)}m²-{C(R^3d)(R^4d)}m³-{C(R^3e)(R^4e)}m⁴-C(R^3f)(R^4f)- (in which, R^3a to R^4e represent hydrogen or the like); T⁰ represents a carbonyl group or the like; and T¹ represents -COCONR- or the like]; or salt thereof, solvate thereof, or N-oxide thereof.The compound is useful as a preventive and/or therapeutic agent for cerebral infarction, cerebral embolism, myocardial infarction, angina pectoris, pulmonary infarction, pulmonary embolism, Buerger’s disease, deep venous thrombosis, disseminated intravascular coagulation syndrome, thrombus formation after valve or joint replacement, thrombus formation and reocclusion after angioplasty, systemic inflammatory response syndrome (SIRS), multiple organ dysfunction syndrome (MODS), thrombus formation during extracorporeal circulation, or blood clotting upon blood drawing.

A compound represented by the following formula (1):Q1-Q2-To-N(R1)-Q3-N(R2)-T1-Q4 [wherein, R¹ and R² are hydrogen atoms or the like; Q¹ is a saturated or unsaturated, 5- or 6- membered cyclic hydrocarbon group which may have a substituent, or the like; Q² is a single bond or the like; Q³ represents the following group: -C(R^3a)(R^4a)-{C(R^3b)(R^4b)}m¹-{C(R^3c)(R^4c)}m²-{C(R^3d)(R^4d)}m³-{C(R^3e)(R^4e)}m⁴-C(R^3f)(R^4f)- (in which, R^3a to R^4e represent hydrogen or the like); T⁰ represents a carbonyl group or the like; and T¹ represents -COCONR- or the like]; or salt thereof, solvate thereof, or N-oxide thereof.The compound is useful as a preventive and/or therapeutic agent for cerebral infarction, cerebral embolism, myocardial infarction, angina pectoris, pulmonary infarction, pulmonary embolism, Buerger’s disease, deep venous thrombosis, disseminated intravascular coagulation syndrome, thrombus formation after valve or joint replacement, thrombus formation and reocclusion after angioplasty, systemic inflammatory response syndrome (SIRS), multiple organ dysfunction syndrome (MODS), thrombus formation during extracorporeal circulation, or blood clotting upon blood drawing.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 216959-94-3. In my other articles, you can also check out more blogs about 216959-94-3

Reference£º
Thiazole | C3H4572NS – PubChem,
Thiazole | chemical compound | Britannica