| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V39203 | (R)-SCH 42495 | 156792-25-5 | (R)-SCH 42495 is a less active isomer of SCH 42495. |
|
V30957 | (R)-Serine | 312-84-5 | D-Serine ((R)-Serine) is an endogenous amino acid (AA) with unique neurotransmitter properties involved in glial-synaptic interactions and is a potent co-agonist of NMDA glutamate receptors. |
|
V33207 | (R)-Simurosertib | 1330782-69-8 | (R)-Simurosertib ((R)-TAK-931) is the R-enantiomer of Simurosertib. |
|
V39219 | (R)-TCO-OH | 39637-78-0 | (R)-TCO-OH is a PROTAC (PROteolysis TArgeting Chimera) linker of the alkyl chain category, may be utilized to prepare PROTAC protein degraders. |
|
V40382 | (R)-Terazosin | 109351-34-0 | R)-Terazosin is the R-enantiomer of Terazosin,which is a selective α1-adrenoceptor antagonist approved for use in treatment of symptoms of BPH (benign prostatic hyperplasia, an enlarged prostate). |
|
V40694 | (R)-Thalidomide | 2614-06-4 | (R)-Thalidomide ((R)-(+)-Thalidomide) is the R-enantiomer of Thalidomide. |
|
V31901 | (R)-UT-155 | 2031161-54-1 | (R)-UT-155 (compound 11) is a selective androgen receptor degradant (SARD) ligand. |
|
V41840 | (R)-Valiolamine Voglibose | 1303996-67-9 | (R)-Valiolamine Voglibose, alpha-glucosidase inhibitor; treat diabetes mellitus |
|
|
V40745 | (R)-Verapamil D7 HCl | (R)-Verapamil D7 HCl is a novel and potent euterated form of (R)-Verapamil HCl | |
|
V40744 | (R)-Verapamil HCl | 38176-02-2 | (R)-Verapamil HCl, the hydrochloride salt of Verapamil R-isomer, is a novel and potent P-Glycoprotein(MRP1, efflux pump in multidrug resistant tumor cells)inhibitor. |
|
V38804 | (R,R)-(+)-Hydrobenzoin | 52340-78-0 | (R,R)-(+)-Hydrobenzoin is an organic catalyst. |
|
V40502 | (R,R)-Glycopyrrolate | 475468-09-8 | R,R)-Glycopyrrolate is a novel and potent anticholinergic agent that is able toreduce the frequency of drooling in vivo with developmental disabilities. |
|
V38636 | (Rac)-3′-Hydroxy simvastatin | 126313-98-2 | Rac)-3′-Hydroxy simvastatin is a major metabolite of Simvastatin which isa competitive inhibitor of HMG-CoA reductase with a Ki of 0.2 nM. |
|
V40297 | (Rac)-5-Keto Fluvastatin | 1160169-39-0 | (Rac)-5-Keto Fluvastatin(3-Hydroxy-5-Keto Fluvastatin) is an impurity of Fluvastatin, which is a HMG-CoA reductase inhibitor with an IC50 of 8 nM. |
|
V40511 | (Rac)-ABT-202 diHCl | 1258641-38-1 | (Rac)-ABT-202 diHCl is the racemate of ABT-202. |
|
V40653 | (Rac)-Acolbifene | 151533-34-5 | (Rac)-Acolbifene (EM-343; (Rac)-EM-652) is the racemic form of EM652 (estrogen receptor blocker (antagonist)) with anti-estrogenic and estrogenic activity. |
|
V39059 | (Rac)-AMG8379 | 1641574-26-6 | (Rac)-AMG8379 ((Rac)-AMG8380) is the racemate of AMG8379. |
|
|
V40270 | (Rac)-Atomoxetine D7 HCl | (Rac)-Atomoxetine D7 HCl is a novel and potent deuterated form of (Rac)-Atomoxetine HCl | |
|
V38631 | (Rac)-Azide-phenylalanine | 1822572-56-4 | (Rac)-Azide-phenylalanine is the racemate of Azide-phenylalanine. |
|
V40153 | (Rac)-BAY-985 | 2101925-20-4 | (Rac)-BAY-985 (example compound 100.01) is a potent, ATP-competitive, and selective TBK1 inhibitor (antagonist) with IC50 of 1.5 nM. |
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