CAS 13849-08-6
:Marmesin
Formel:C14H14O4
InChl:InChI=1S/C14H14O4/c1-14(2,16)12-6-9-5-8-3-4-13(15)18-10(8)7-11(9)17-12/h3-5,7,12,16H,6H2,1-2H3/t12-/m0/s1
InChI Key:InChIKey=FWYSBEAFFPBAQU-LBPRGKRZSA-N
SMILES:C(C)(C)(O)[C@@H]1CC=2C(=CC3=C(C2)C=CC(=O)O3)O1
Synonyme:- (2R)-2-(2-hydroxypropan-2-yl)-2,3-dihydro-7H-furo[3,2-g]chromen-7-one
- (2S)-2,3-Dihydro-2-(1-hydroxy-1-methylethyl)-7H-furo[3,2-g][1]benzopyran-7-one
- (2S)-2-(2-hydroxypropan-2-yl)-2,3-dihydro-7H-furo[3,2-g]chromen-7-one
- (S)-Marmesin
- 2-(2-hydroxypropan-2-yl)-2,3-dihydro-7H-furo[3,2-g]chromen-7-one
- 7H-Furo(3,2-g)(1)benzopyran-7-one, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (S)-(+)-
- 7H-Furo[3,2-g][1]benzopyran-7-one, 2,3-dihydro-2-(1-hydroxy-1-methylethyl)-, (2S)-
- Ccris 5728
- Nsc 340840
- Marmesin
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S-(+)-Marmesin
CAS:S-(+)-MarmesinFormel:C14H14O4Reinheit:≥98%Farbe und Form:SolidMolekulargewicht:246.26S-(+)-Marmesin (Standard)
CAS:S-(+)-Marmesin (Standard) is a reference standard for research and analysis in studies involving S-(+)-Marmesin. S-(+)-Marmesin (marmesin) is a coumarin originally isolated from the mature bark of A. marmelos,exhibiting COX-2/5-LOX dual inhibitory activity.Formel:C14H14O4Molekulargewicht:246.2586Marmesin
CAS:(S)-2-(2-Hydroxypropan-2-yl)-2,3-dihydro-7H-furo[3,2-g]chromen-7-oneFormel:C14H14O4Reinheit:98%Molekulargewicht:246.26S-(+)-Marmesin
CAS:S-(+)-Marmesin (marmesin) is a coumarin originally isolated from the mature bark of A. marmelos,exhibiting COX-2/5-LOX dual inhibitory activity.Formel:C14H14O4Reinheit:98.00% - ≥98%Farbe und Form:SolidMolekulargewicht:246.2586(+)-Marmesin
CAS:LactoneFormel:C14H14O4Reinheit:≥ 90.0 % (HPLC)Farbe und Form:PowderMolekulargewicht:246.26Marmesin
CAS:Marmesin is a polymerase chain inhibitor that binds to the DNA-dependent RNA polymerase and prevents transcription and replication. It has been shown to be active against infectious diseases such as HIV, influenza, Ebola, and herpes simplex virus. Marmesin has also been shown to inhibit the production of reactive oxygen species (ROS) in cells by binding to reactive oxygen species and preventing their interactions with cellular components. The drug has been found to have a matrix effect on hl-60 cells, which may be due to its ability to inhibit the apoptosis pathway. In addition, marmesin has been found to have high affinity for molecular docking analysis with oral pathogens such as Streptococcus mutans and Streptococcus sobrinus.Formel:C14H14O4Reinheit:Min. 95%Farbe und Form:White PowderMolekulargewicht:246.26 g/mol(S)-2-(2-Hydroxypropan-2-yl)-2H-furo[3,2-g]chromen-7(3H)-one
CAS:Formel:C14H14O4Reinheit:98%Molekulargewicht:246.2586









