Product Name :
H-PGDS Inhibitor I
Description:
H-PGDS INHIBITOR I is a Prostaglandin D Synthase (hematopoietic-type) Inhibitor. H-PGDS INHIBITOR I has no code name, and has CAS#1033836-12-2. The last 5-digit was used for name for easy communication. H-PGDS INHIBITOR I selectively blocks HPGDS (IC50s = 0.7 and 32 nM in enzyme and cellular assays, respectively) with little activity against the related human enzymes L-PGDS, mPGES, COX-1, COX-2, and 5-LOX.
CAS:
1033836-12-2
Molecular Weight:
381.37
Formula:
C19H19F4N3O
Chemical Name:
6-(3-fluorophenyl)-N-[1-(2,2,2-trifluoroethyl)-4-piperidinyl]-3-pyridinecarboxamide
Smiles :
O=C(NC1CCN(CC(F)(F)F)CC1)C1=CN=C(C=C1)C1=CC(F)=CC=C1
InChiKey:
LPUCBGGXXIUBAZ-UHFFFAOYSA-N
InChi :
InChI=1S/C19H19F4N3O/c20-15-3-1-2-13(10-15)17-5-4-14(11-24-17)18(27)25-16-6-8-26(9-7-16)12-19(21,22)23/h1-5,10-11,16H,6-9,12H2,(H,25,27)
Purity:
≥98% (or refer to the Certificate of Analysis)
Shipping Condition:
Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis
Storage Condition :
Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.
Shelf Life:
≥12 months if stored properly.
Stock Solution Storage:
0 – 4 oC for 1 month or refer to the Certificate of Analysis.
Additional information:
H-PGDS INHIBITOR I is a Prostaglandin D Synthase (hematopoietic-type) Inhibitor. H-PGDS INHIBITOR I has no code name, and has CAS#1033836-12-2. The last 5-digit was used for name for easy communication. H-PGDS INHIBITOR I selectively blocks HPGDS (IC50s = 0.7 and 32 nM in enzyme and cellular assays, respectively) with little activity against the related human enzymes L-PGDS, mPGES, COX-1, COX-2, and 5-LOX.{{Hesperetin} MedChemExpress|{Hesperetin} Autophagy|{Hesperetin} Technical Information|{Hesperetin} Description|{Hesperetin} supplier|{Hesperetin} Cancer} |Product information|CAS Number: 1033836-12-2|Molecular Weight: 381.37|Formula: C19H19F4N3O|Synonym:|MDK36122|MDK-36122|Prostaglandin D Synthase (hematopoietic-type) Inhibitor I|PGDS Inhibitor I|Chemical Name: 6-(3-fluorophenyl)-N-[1-(2,2,2-trifluoroethyl)-4-piperidinyl]-3-pyridinecarboxamide|Smiles: O=C(NC1CCN(CC(F)(F)F)CC1)C1=CN=C(C=C1)C1=CC(F)=CC=C1|InChiKey: LPUCBGGXXIUBAZ-UHFFFAOYSA-N|InChi: InChI=1S/C19H19F4N3O/c20-15-3-1-2-13(10-15)17-5-4-14(11-24-17)18(27)25-16-6-8-26(9-7-16)12-19(21,22)23/h1-5,10-11,16H,6-9,12H2,(H,25,27)|Technical Data|Appearance: Solid Power.|Purity: ≥98% (or refer to the Certificate of Analysis)|Solubility: Soluble in DMSO|Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis|Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.|Shelf Life: ≥12 months if stored properly.|Stock Solution Storage: 0 – 4 oC for 1 month or refer to the Certificate of Analysis.|Drug Formulation: To be determined.|HS Tariff Code: 382200|How to use|In Vitro:|HPGDS inhibitor 1 has equal potency against purified HPGDS from human, rat, dog, and sheep (IC50, 0.5-2.3 nM).|In Vivo:|HPGDS inhibitor 1 (compound 8; 1 mg/kg) has excellent PK characteristics with 76% bioavailability, and the T1/2 is 4.{{Anidulafungin} web|{Anidulafungin} Anti-infection|{Anidulafungin} Protocol|{Anidulafungin} References|{Anidulafungin} supplier|{Anidulafungin} Autophagy} 1 hours in rats.PMID:23771862 Rats dosed orally with 1 mg/kg and 10 mg/kg HPGDS inhibitor 1 (compound 8) are sacrificed at various times. Oral administration of HPGDS inhibitor 1 blocks PGD2 production in the rat spleen; inhibition of PGD2 is inversely correlated with the plasma concentration of HPGDS inhibitor 1 in a time- and dose-dependent manner. HPGDS inhibitor 1 (compound 8; 1 mg/mL) illustrates efficacy in an in vivo sheep model of asthma.|References:|Carron CP, Trujillo JI, Olson KL, Huang W, Hamper BC, Dice T, Neal BE, Pelc MJ, Day JE, Rohrer DC, Kiefer JR, Moon JB, Schweitzer BA, Blake TD, Turner SR, Woerndle R, Case BL, Bono CP, Dilworth VM, Funckes-Shippy CL, Hood BL, Jerome GM, Kornmeier CM, Radabaugh MR, Williams ML, Davies MS, Wegner CD, Welsch DJ, Abraham WM, Warren CJ, Dowty ME, Hua F, Zutshi A, Yang JZ, Thorarensen A. Discovery of an Oral Potent Selective Inhibitor of Hematopoietic Prostaglandin D Synthase (HPGDS). ACS Med Chem Lett. 2010 Feb 2;1(2):59-63. doi: 10.1021/ml900025z. eCollection 2010 May 13. PubMed PMID: 24900177; PubMed Central PMCID: PMC4007851.Products are for research use only. Not for human use.|
