Metabolism
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Products Related to Metabolism(2997)
- GC796871-Palmitoyl-2-oleoyl-sn-glycero-3-PSCAS: 40290-44-6Purity: >99.50%
2-Oleoyl-1-palmitoyl-sn-glycero-3-phospho-L-serine (16:0-18:1 PS (POPS) free acid) is an anionic phospholipid with oleic acid (18:1) and palmitic acid (16:0) tails containing a carboxylic acid (COOH) and amine (NH2) in their head group.
- GC79688MeDZ lipidPurity: >98%
MeDZ lipid is a zwitterion-type ionizable endosomal membrane destabilizer and anti-inflammatory agent that promotes endosomal escape.
- GC79689PI(3,5)P2 diC16CAS: 214282-36-7Purity: >98%
PI(3,5)P2 diC16 is a synthetic inositol phospholipid.
- GC79690AA76-lipidPurity: >99.50%
AA76-lipid (Compound aa76) is a compound with a C-terminal arginine and histidine.
- GC79691mPEG2000-DPGCAS: 162409-28-1Purity: >98.00%
mPEG2000-DPG is a PEG-based lipid that can be used to formulate lipid nanoparticles for drug delivery.
- GC79692DSPE-PEG2000-tetrazineCAS: 3101670-39-4Purity: >98%
DSPE-PEG2000-tetrazine is a synthetic phospholipid modified with PEG2000 and tetrazine moieties.
- GC79693DSG-PEG2000-OHPurity: >95.00%
DSG-PEG2000-OH is a conjugate composed of dimyristic glycerol (DMG), a PEG chain, and terminal hydroxyl groups (-OH).
- GC79694Lipopeptide CPK4 TFAPurity: >98.50%
Lipopeptide CPK4 TFA is a Cholesterol -modified peptide K4 [(KIAALKE) 3 ]. Lipopeptide CPK4 TFA is capable of coiled-coil formation when attached to liposomes.
- GC79695Lipopeptide CPE4 TFAPurity: >98.50%
Lipopeptide CPE4 TFA is a PEG-modified peptide E4 [(EIAALEK) 4 ]. Lipopeptide CPE4 TFA is capable of coiled-coil formation when attached to liposomes.
- GC79696DSPE-PEG3400-MTPPurity: >95.00%
DSPE-PEG3400-MTP is a PEG compound which composed of DSPE and a muscle-targeting peptide (MTP).
- GC79697DSPE-PEG3400-GNYTCEVTELTREGETIIELKPurity: >98.00%
DSPE-PEG3400-GNYTCEVTELTREGETIIELK is a PEG compound which composed of DSPE and a peptide mimicking the function of CD47 (GNYTCEVTELTREGETIIELK).
- GC79698DSPE-PEG2000-VHPKQHRGGSKGCPurity: >95.00%
DSPE-PEG2000-VHPKQHRGGSKGC is a targeted modified phospholipid-polyethylene glycol conjugate covalently coupled to DSPE, PEG, and the vascular-targeting peptide VHPKQHRGGSKGC.
- GC79699DSPE-PEG2000-MTPPurity: >95.00%
DSPE-PEG2000-MTP is a PEG compound which composed of DSPE and a muscle-targeting peptide (MTP).
- GC79700DSPE-PEG2000-Mal-Cys-penetratinPurity: >95.00%
DSPE-PEG2000-Mal-Cys-penetratin is a conjugate composed of DSPE, a PEG chain, and terminal maleimide (Mal).
- GC79701DSPE-PEG2000-KTPPurity: >98%
DSPE-PEG2000-KTP is a PEG compound which composed of DSPE and a Kidney-targeting peptide KTP.
- GC79702DSPE-PEG2000-CTPPurity: >95.00%
DSPE-PEG2000-CTP is a PEG compound which composed of DSPE and a Cardiac-targeting peptide CTP.
- GC79703DSPE-PEG1000-GNYTCEVTELTREGETIIELKPurity: >98.00%
DSPE-PEG1000-GNYTCEVTELTREGETIIELK is a PEG compound which composed of DSPE and a peptide mimicking the function of CD47 (GNYTCEVTELTREGETIIELK).
- GC79704DPPE-PEG2000-MalPurity: >98.00%
DPPE-PEG2000-Mal is a conjugate composed of DPPE, PEG chains, and maleimide (Mal).
- GC79705DMG-PEG2000-Mal-Cys-penetratinPurity: >95.00%
DMG-PEG2000-Mal-Cys-penetratin is a conjugate composed of dimyristoylglycerol (DMG), a PEG chain, and terminal maleimide (Mal).
- GC79723AlofropodectCAS: 1829530-11-1Purity: >98%
Alofropodect is an orally active, blood-brain barrier permeable phosphodiesterase 10A ( PDE10A ) inhibitor with IC 50 values of 1 nM (Reference 1) and 35 nM (Reference 2).
- GC79731Daunorubicin-Cytarabine LiposomeCAS: 1256639-86-7Purity: >98%
Cytarabine -daunorubicin (CPX 351) is a Liposomal formulation prepared from Cytarabine and Daunorubicin at a fixed synergistic molar ratio of 5:1.
- GC79743PDE1-IN-11CAS: 86009-41-8Purity: >99.00%
PDE1-IN-11 (Compound 5cc) is an orally active and highly selective PDE1A1 inhibitor.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC79687 | 1-Palmitoyl-2-oleoyl-sn-glycero-3-PS | 40290-44-6 | >99.50% | |
2-Oleoyl-1-palmitoyl-sn-glycero-3-phospho-L-serine (16:0-18:1 PS (POPS) free acid) is an anionic phospholipid with oleic acid (18:1) and palmitic acid (16:0) tails containing a carboxylic acid (COOH) and amine (NH2) in their head group. | ||||
| GC79688 | MeDZ lipid | - | >98% | |
MeDZ lipid is a zwitterion-type ionizable endosomal membrane destabilizer and anti-inflammatory agent that promotes endosomal escape. | ||||
| GC79689 | PI(3,5)P2 diC16 | 214282-36-7 | >98% | |
PI(3,5)P2 diC16 is a synthetic inositol phospholipid. | ||||
| GC79690 | AA76-lipid | - | >99.50% | |
AA76-lipid (Compound aa76) is a compound with a C-terminal arginine and histidine. | ||||
| GC79691 | mPEG2000-DPG | 162409-28-1 | >98.00% | |
mPEG2000-DPG is a PEG-based lipid that can be used to formulate lipid nanoparticles for drug delivery. | ||||
| GC79692 | DSPE-PEG2000-tetrazine | 3101670-39-4 | >98% | |
DSPE-PEG2000-tetrazine is a synthetic phospholipid modified with PEG2000 and tetrazine moieties. | ||||
| GC79693 | DSG-PEG2000-OH | - | >95.00% | |
DSG-PEG2000-OH is a conjugate composed of dimyristic glycerol (DMG), a PEG chain, and terminal hydroxyl groups (-OH). | ||||
| GC79694 | Lipopeptide CPK4 TFA | - | >98.50% | |
Lipopeptide CPK4 TFA is a Cholesterol -modified peptide K4 [(KIAALKE) 3 ]. Lipopeptide CPK4 TFA is capable of coiled-coil formation when attached to liposomes. | ||||
| GC79695 | Lipopeptide CPE4 TFA | - | >98.50% | |
Lipopeptide CPE4 TFA is a PEG-modified peptide E4 [(EIAALEK) 4 ]. Lipopeptide CPE4 TFA is capable of coiled-coil formation when attached to liposomes. | ||||
| GC79696 | DSPE-PEG3400-MTP | - | >95.00% | |
DSPE-PEG3400-MTP is a PEG compound which composed of DSPE and a muscle-targeting peptide (MTP). | ||||
| GC79697 | DSPE-PEG3400-GNYTCEVTELTREGETIIELK | - | >98.00% | |
DSPE-PEG3400-GNYTCEVTELTREGETIIELK is a PEG compound which composed of DSPE and a peptide mimicking the function of CD47 (GNYTCEVTELTREGETIIELK). | ||||
| GC79698 | DSPE-PEG2000-VHPKQHRGGSKGC | - | >95.00% | |
DSPE-PEG2000-VHPKQHRGGSKGC is a targeted modified phospholipid-polyethylene glycol conjugate covalently coupled to DSPE, PEG, and the vascular-targeting peptide VHPKQHRGGSKGC. | ||||
| GC79699 | DSPE-PEG2000-MTP | - | >95.00% | |
DSPE-PEG2000-MTP is a PEG compound which composed of DSPE and a muscle-targeting peptide (MTP). | ||||
| GC79700 | DSPE-PEG2000-Mal-Cys-penetratin | - | >95.00% | |
DSPE-PEG2000-Mal-Cys-penetratin is a conjugate composed of DSPE, a PEG chain, and terminal maleimide (Mal). | ||||
| GC79701 | DSPE-PEG2000-KTP | - | >98% | |
DSPE-PEG2000-KTP is a PEG compound which composed of DSPE and a Kidney-targeting peptide KTP. | ||||
| GC79702 | DSPE-PEG2000-CTP | - | >95.00% | |
DSPE-PEG2000-CTP is a PEG compound which composed of DSPE and a Cardiac-targeting peptide CTP. | ||||
| GC79703 | DSPE-PEG1000-GNYTCEVTELTREGETIIELK | - | >98.00% | |
DSPE-PEG1000-GNYTCEVTELTREGETIIELK is a PEG compound which composed of DSPE and a peptide mimicking the function of CD47 (GNYTCEVTELTREGETIIELK). | ||||
| GC79704 | DPPE-PEG2000-Mal | - | >98.00% | |
DPPE-PEG2000-Mal is a conjugate composed of DPPE, PEG chains, and maleimide (Mal). | ||||
| GC79705 | DMG-PEG2000-Mal-Cys-penetratin | - | >95.00% | |
DMG-PEG2000-Mal-Cys-penetratin is a conjugate composed of dimyristoylglycerol (DMG), a PEG chain, and terminal maleimide (Mal). | ||||
| GC79710 | ATX-012 | 1777792-44-5 | >98% | |
ATX-012 is an ionizable cationic lipid for the assembly of mRNA -delivering lipid nanoparticles (LNPs). | ||||
| GC79722 | Escholtzine perchlorate | 77790-29-5 | >98.00% | |
Escholtzine perchlorate is an Alkaloid. | ||||
| GC79723 | Alofropodect | 1829530-11-1 | >98% | |
Alofropodect is an orally active, blood-brain barrier permeable phosphodiesterase 10A ( PDE10A ) inhibitor with IC 50 values of 1 nM (Reference 1) and 35 nM (Reference 2). | ||||
| GC79731 | Daunorubicin-Cytarabine Liposome | 1256639-86-7 | >98% | |
Cytarabine -daunorubicin (CPX 351) is a Liposomal formulation prepared from Cytarabine and Daunorubicin at a fixed synergistic molar ratio of 5:1. | ||||
| GC79743 | PDE1-IN-11 | 86009-41-8 | >99.00% | |
PDE1-IN-11 (Compound 5cc) is an orally active and highly selective PDE1A1 inhibitor. | ||||
