![3-Oxoacyl-[acyl-carrier-protein] reductase](https://file.medchemexpress.com/product_pic/hy-e71774.gif "Click to View 3-Oxoacyl-[acyl-carrier-protein] reductase Product Detail")
Scientific Reviews
Product Guides
Blogs
Topics
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
35 Results for "
NADPH-dependent 3
" in MedChemExpress (MCE) Product Catalog:
Products (35)
35 Results for "NADPH-dependent 3" in MCE Product Catalog:
Cat. No.: HY-P80590A
Synonyms: 15 hydroxyprostaglandin dehydrogenase [NADP ]; 15-hydroxyprostaglandin dehydrogenase [NADP ]; Carbonyl reductase [NADPH] 1; CBR 1; CBR1; CBR1_HUMAN; CRN; NADPH dependent carbonyl reductase 1; NADPH-dependent carbonyl reductase 1; Prostaglandin 9 ketoreduc
Cat. No.: HY-E71774
Target:
Research Areas:
3-Oxoacyl-[acyl-carrier-protein] reductase (EC 1.1.1.100) is an NADPH-dependent β-ketoacyl-ACP reductase and a key enzyme in the bacterial type II fatty acid synthesis pathway.
Cat. No.: HY-P76172
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: BLVRB; Green Heme-Binding Protein; Prev. FLR; GHBP; S-Nitroso-CoA-Assisted Nitrosyltransferase; FR; Biliverdin-IX Beta-Reductase; Biliverdin Reductase B (Flavin Reductase (NADPH)); NADPH-dependent Diaphorase; Epididymis Secretory Protein Li 10; Flavin Red
Species:
Human
Source:
E. coli
Cat. No.: HY-187119
CAS No.: 158575-73-6
Target:
Research Areas:
CC13401 is an aldose reductase (ALR2) inhibitor with an IC50 of 41.41 μM in rats. CC13401 inhibits the NADPH-dependent reduction reaction catalyzed by ALR2. CC13401 can be used in studies on the mechanisms related to the polyol pathway and diabetic complications .
Cat. No.: HY-P85567
Synonyms: 15 hydroxyprostaglandin dehydrogenase [NADP ]; 15-hydroxyprostaglandin dehydrogenase [NADP ]; Carbonyl reductase [NADPH] 1; CBR 1; CBR1; CBR1_HUMAN; CRN; NADPH dependent carbonyl reductase 1; NADPH-dependent carbonyl reductase 1; Prostaglandin 9 ketoreductase; Prostaglandin 9-ketoreductase; Prostaglandin E; 2; 9 reductase; Prostaglandin-E; 2; 9-reductase; SDR21C1.
Cat. No.: HY-E71567
Target:
Research Areas:
2-Hydroxymethylglutarate dehydrogenase (EC 1.1.1.291) is an NADPH-dependent D-ribulose reductase—a type of oxidoreductase—that catalyzes the reduction of D-ribulose to D-arabitol. It plays a key role in pentose metabolism, sugar alcohol metabolism, and carbon source utilization in microorganisms and fungi.
Cat. No.: HY-E71653
Target:
Research Areas:
3,9-Dihydroxypterocarpan 6a-monooxygenase (EC 1.14.13.28) is a plant cytochrome P450 monooxygenase that hydroxylates 3,9-dihydroxypterocarpan via an NADPH-dependent oxidation reaction, participating in the biosynthesis of glyceollin—a disease-resistance metabolite found in legumes such as soybean.
Cat. No.: HY-187733
CAS No.: 77016-85-4
Target:
Research Areas:
Plomestane is an orally active second-generation steroidal aromatase inhibitor that, as an enzyme-activated pseudosubstrate, is converted via NADPH-dependent catalysis into a reactive intermediate, which covalently binds to aromatase to produce irreversible inhibition, thereby persistently suppressing peripheral aromatase activity. Plomestane can be used for the study of hormone-dependent breast cancer .
Cat. No.: HY-P704102
Purity: ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: VAT1L; Vesicle Amine Transport 1 Like; KIAA1576; Vesicle Amine Transport Protein 1 Homolog (T. California)-Like; Putative NADPH-dependent Quinone Oxidoreductase VAT1L; Synaptic Vesicle Membrane Protein VAT-1 Homolog-Like; Vesicle Amine Transport Protein 1
Species:
Human
Source:
E. coli
Cat. No.: HY-E71772A
Target:
Research Areas:
3-Oxo-5-β-steroid 4-dehydrogenase from human (Recombinant) (EC 1.3.1.3) belongs to the NADPH-dependent short-chain dehydrogenase/reductase superfamily (AKR family). It catalyzes the 5β-reduction of the Δ4 double bond in steroid molecules and is involved in bile acid synthesis and steroid hormone metabolism, serving as a crucial enzyme for maintaining hepatic cholesterol metabolism and endocrine homeostasis.
Cat. No.: HY-P72272
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CBR1; Carbonyl Reductase [NADPH] 1; Prev. CBR; Short Chain Dehydrogenase/Reductase Family 21C, Member 1; SDR21C1; 15-Hydroxyprostaglandin Dehydrogenase [NADP(+)]; Short Chain Dehydrogenase/Reductase Family 21C Member 1; Epididymis Secretory Sperm Binding Protein; 20-Beta-Hydroxysteroid Dehydrogenase; 15-Hydroxyprostaglandin Dehydrogenase; NADPH-dependent Carbonyl Reductase 1; Carbonyl Reductase (NADPH) 1; Alcohol Dehydrogenase [NAD(P)+] CBR1; Carbonyl Reductase (NADPH); Prostaglandin-E(2) 9-Reductase; HCBR1; Prostaglandin 9-Ketoreductase; CRN; Carbonyl Reductase 1; PG-9-KR
Species:
Human
Source:
P. pastoris
Cat. No.: HY-122940R
CAS No.: 644-06-4
Synonyms: Ageratochromene (Standard)
Category:
Cat. No.: HY-187975
CAS No.: 917613-59-3
Target:
Research Areas:
MT-1207 free base is an orally active, selective adrenergic α1 and 5-HT2A receptor antagonist. MT-1207 has IC50 values of <0.1 nM, 0.15 nM, 1.40 nM, and 0.27 nM for α1A, α1B, α1D, and 5-HT2A, respectively. MT-1207 free base induces vasodilation, improves baroreflex sensitivity, and reduces heart rate in isolated hearts. MT-1207 free base lowers blood pressure, protects the heart, brain, and kidneys, improves cognition, delays stroke, reduces mortality, and lowers uric acid without impairing renal function in SHR/2K1C/2K2C models. MT-1207 free base exhibits high plasma protein binding, resistance to plasma esterases, and NADPH-dependent hepatic metabolism. MT-1207 free base can be used for research related to hypertension [3].
Target:
Research Areas:
L-Lactaldehyde ((2S)-Hydroxypropanal) is a chiral aldehyde, metabolic intermediate, and enzyme substrate. L-Lactaldehyde is oxidized to L-lactate by NAD-dependent lactaldehyde dehydrogenase. L-Lactaldehyde is reduced to L-1,2-propanediol by NADH/NADPH-dependent oxidoreductases. L-Lactaldehyde is used in studies of microbial sugar metabolism and carbonyl metabolism [3].
Cat. No.: HY-P701217
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PTGR1; ZADH3; Prev. LTB4DH; D3T-Inducible Gene 1 Protein; Leukotriene B4 12-Hydroxydehydrogenase; DIG-1; NAD(P)H-dependent Alkenal/One Oxidoreductase; PRG-1; Dithiolethione-Inducible Gene 1 Protein; NADP-dependent Leukotriene B4 12-Hydroxydehydrogenase; 1
Species:
Human
Source:
HEK293
- 1
- 2
-
-
Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
