79 Results for "

Inactive ,metabolite

" in MedChemExpress (MCE) Product Catalog:
Products (79)

79 Results for "Inactive ,metabolite" in MCE Product Catalog:

Cat. No.: HY-113164
CAS No.: 25486-55-9
Purity:  99.99%
Target:  

Endogenous Metabolite

Research Areas:  

Others

Vitamin K1 2,3-epoxide is an inactive metabolite form of Vitamin K1 (HY-N0684), which is reduced to active vitamin by microsomal epoxide reductase in the vitamin K epoxide cycle. Vitamin K1 2,3-epoxide is involved in blood clotting .
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Cat. No.: HY-126373S1
Synonyms: SN-38G-13C6
SN-38 glucuronide- 13C6 is the 13C labeled SN-38 glucuronide (HY-126373) . SN-38 glucuronide is an inactive metabolite of the cancer agent Irinotecan. Irinotecan is a topoisomerase I inhibitor which can be used for researching colon and rectal cancer .
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Cat. No.: HY-126619
CAS No.: 71968-02-0
Target:  

Bacterial Apoptosis

Research Areas:  

Infection

Aspochalasin D is a co-metabolite originally isolated from A. microcysticus with aspochalasins A, B, and C, that is initially thought to be inactive. It has antibacterial activity against Gram-positive and Gram-negative bacteria at a concentration of 1 mg/ml.2 Aspochalasin D is more cytotoxic, via apoptosis, to Ba/F3-V12 cells in an IL-3-free medium than in an IL-3-containing medium (IC50s=0.49 and 1.9 μg/mL, respectively).
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Cat. No.: HY-W059917
CAS No.: 1300690-48-5
Target:  

Drug Metabolite

Research Areas:  

Others

AP24600 is an inactive metabolite of Ponatinib .
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Cat. No.: HY-N0929R
CAS No.: 36062-05-2
Hexahydrocurcumin (Standard) is the analytical standard of Hexahydrocurcumin. This product is intended for research and analytical applications. Hexahydrocurcumin is one of the major metabolites of curcumin and a selective, orally active COX-2 inhibitor. Hexahydrocurcumin is inactive against COX-1. Hexahydrocurcumin has antioxidant, anticancer and anti-inflammatory activities .
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Cat. No.: HY-137555
CAS No.: 79250-60-5
Purity:  ≥99.0%
Synonyms: 11-dehydro-2,3-dinor TXB2
Target:  

Endogenous Metabolite

Research Areas:  

Metabolic Disease

11-dehydro-2,3-dinor Thromboxane B2 (11-dehydro-2,3-dinor TXB2) is a metabolite of the TXA2 inactive metabolite TXB2 (Item No. 19030). It is formed from TXB2 by cytosolic aldehyde dehydrogenase (ALDH) and β-oxidation. Levels of 11-dehydro-2,3-dinor TXB2 are increased 5.2-fold in a surgery-induced rat model of tendon overuse.
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Cat. No.: HY-W929472
CAS No.: 87984-82-5
13 (S)-HOTrE is an oxylipin metabolite of α-Linolenic acid (HY-N0728). 13 (S)-HOTrE mediates the inactivation of the NLRP3 inflammasome through the PPAR-γ pathway to exert anti-inflammatory effects. 13 (S)-HOTrE inhibits NF-κB nuclear translocation, ROS production, autophagy and IL-1β levels, induces apoptosis, and increases IL-10 levels. 13 (S)-HOTrE alleviates LPS-induced inflammatory responses in macrophages, prolongs the survival time of septic mice, and regulates the immunometabolic phenotype in parenteral nutrition mouse models. 13 (S)-HOTrE can be used in the research of immune and inflammation-related diseases .
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Cat. No.: HY-W704031
CAS No.: 239466-86-5
Target:  

Drug Metabolite

Research Areas:  

Metabolic Disease

Prasugrel metabolite 1 (M7 (R-119251)) is one of the inactive metabolites of Prasugrel (HY-15284) in the human body .
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Cat. No.: HY-135500
CAS No.: 1433875-14-9
Target:  

Endothelin Receptor

Research Areas:  

Endocrinology

ACT-373898 is an inactive carboxylic acid metabolite of Macitentan. Macitentan is an orally active, non-peptide dual ETA and ETB (endothelin receptor) antagonist .
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Cat. No.: HY-Z4483
CAS No.: 104227-86-3
Target:  

Drug Intermediate

Research Areas:  

Others

6-Deoxypenciclovir is an inactive metabolite of the antiviral prodrug Famciclovir. 6-Deoxypenciclovir is a good substrate for rabbit hepatic aldehyde oxidase and can be used to synthesize the prodrug form of penciclovir .
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Cat. No.: HY-13609S
Deflazacort-d5 is the deuterium labeled Deflazacort. Deflazacort, a glucocorticoid, is an inactive proagent and is converted rapidly to the active metabolite 21-desacetyldeflazacort. Deflazacort is used as an anti-inflammatory and immunosuppressant .
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Cat. No.: HY-134520
CAS No.: 13649-88-2
Research Areas:  

Inflammation/Immunology

21-Deacetoxy deflazacort is a dehydrogenated derivative of Deflazacort (HY-13609), a glucocorticoid, an inactive precursor that is rapidly converted to the active metabolite 21-Desacetyldeflazacort. Deflazacort acts as an anti-inflammatory and immunosuppressant .
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Cat. No.: HY-U00199
CAS No.: 59878-63-6
Synonyms: N-Desmethyl zopiclone; RP 32273
Target:  

Drug Metabolite

Research Areas:  

Neurological Disease

Norzopiclone is the inactive metabolite of Zopiclone. Norzopiclone has some anxiolytic properties.
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Cat. No.: HY-125074
CAS No.: 368891-69-4
Target:  

Drug Metabolite

Research Areas:  

Infection

PNU 142300 is an inactive metabolite of the oxazolidinone antibiotic Linezolid (HY-10394).
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Cat. No.: HY-W740674
CAS No.: 27046-19-1
Research Areas:  

Cancer

4-Ketocyclophosphamide is an inactive metabolite of the alkylating agent Cyclophosphamide (HY-17420).
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Cat. No.: HY-118247
CAS No.: 110675-48-4
Target:  

Drug Metabolite

Research Areas:  

Others

Ro 14-6113 is an inactive phenolic metabolite of the "carotenoid" Ro 15-0778, a form of vitamin A.
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Cat. No.: HY-W585982
CAS No.: 267244-08-6
Research Areas:  

Endocrinology

Bisphenol A-β-D-glucuronide is an inactive metabolite of the plasticizer Bisphenol A (HY-18260) .
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Cat. No.: HY-132186
CAS No.: 384380-52-3
Target:  

HIV

Research Areas:  

Infection

Abacavir carboxylate is an inactive metabolite of the HIV-1 reverse transcriptase inhibitor Abacavir (HY-17423) .
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Cat. No.: HY-135580
CAS No.: 84541-38-8
Target:  

Drug Metabolite

Research Areas:  

Endocrinology

Raloxifene Bismethyl Ether is a metabolite of Raloxifene and an estrogen receptor inactive compound on which both hydroxyl groups are absent .
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Cat. No.: HY-135580A
CAS No.: 84541-36-6
Target:  

Drug Metabolite

Research Areas:  

Endocrinology

Raloxifene Bismethyl Ether hydrochloride is a metabolite of Raloxifene and an estrogen receptor inactive compound on which both hydroxyl groups are absent .
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