40
1
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T28353 | PDP-EA | FAAH | |
PDP-EA is an activator of fatty acid amide hydrolase(FAAH) and enhances the amidohydrolase activity of FAAH. | |||
T18531 | PDP-Pfp | Others | |
PDP-Pfp is a reducible ADC linker primarily utilized for targeting agents aimed at the extracellular loop 1 (ECL1) of TM4SF1, a member of the transmembrane 4 L6 family, as supported by reference [1]. | |||
T18530 | PDP-C1-Ph-Val-Cit | Others | |
PDP-C1-Ph-Val-Cit is a cleavable ADC linker used for antibody-drug conjugates (ADCs). | |||
T74302 | DSPE-PEG-PDP | ||
DSPE-PEG-PDP, a phospholipid-polyethylene glycol (PEG) conjugate, is utilized in drug delivery applications [1]. | |||
T6741 | SPDP | SPDP Crosslinker | Others |
SPDP is a short-chain crosslinker, which is used for amine-to-sulfhydryl conjugation via NHS-ester and pyridyldithiol reactive groups that form cleavable (reducible) disulfide bonds with cysteine sulfhydryls. SPDP could ... | |||
TP2036L | DPDPE TFA (88373-73-3 free base) | DPDPE TFA | Opioid Receptor |
DPDPE TFA is selective δ-opioid receptor agonist peptide. Inhibits electrically stimulated contraction of mouse vas deferens in vitro (EC50 = 5.2 nM), and is antinociceptive in vivo. | |||
T19955 | Biotin-HPDP | Pyridyldisulfide-biotin,Pyridyldithiol-biotin | Others |
Biotin-HPDP (Pyridyldithiol-biotin) is a sulfhydryl reactive biotinylation reagent. | |||
T17834 | DM4-SPDP | Others | |
DM4-SPDP, a drug-linker conjugate, integrates the antitubulin agent DM4 with the linker SMCC, facilitating the creation of antibody drug conjugates[1]. Additionally, SPDP serves as a short-chain crosslinker enabling amin... | |||
T18715 | SPDP-PEG7-acid | Others | |
SPDP-PEG7-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system wi... | |||
T18714 | SPDP-PEG5-acid | Others | |
SPDP-PEG5-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system wi... | |||
T16918 | SPDP-PEG6-NHS ester | Others | |
SPDP-PEG6-NHS ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome syst... | |||
T18712 | SPDP-PEG24-NHS ester | Others | |
SPDP-PEG24-NHS ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome sys... | |||
T35493 | (±)10(11)-EpDPA | ||
Cytochrome P450 metabolism of polyunsaturated fatty acids produces numerous bioactive epoxide regioisomers. (±)10(11)-EpDPA is a docosahexaenoic acid epoxygenase metabolite, derived via epoxidation of the 10,11-double bo... | |||
T37235 | (±)16(17)-EpDPA | (±)16,17-EpDPE,(±)16,17 EDP,(±)16,17-epoxy Docosapentaenoic Acid,(±)16,17-epoxy DPA,(±)16(17)-EpDPA | |
EDHF (endothelium-derived hyperpolarizing factor) is an unidentified mediator released from vascular endothelial cells in response to acetylcholine and bradykinin which is distinct from the NOS- (nitric oxide) and COX-de... | |||
T18535 | PEG4-SPDP | Others | |
PEG4-SPDP is a cleavable ADC linker used for the antibody-drug conjugates (ADCs). | |||
T18733 | Sulfo-SPDP-C6-NHS sodium | Others | |
Sulfo-SPDP-C6-NHS sodium is a sodium salt form of a cleavable ADC linker employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T18709 | SPDP-PEG12-acid | Others | |
SPDP-PEG12-acid is a cleavable 12-unit polyethylene glycol (PEG) linker utilized for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
TP2036 | DPDPE | Opioid Receptor | |
DPDPE is selective δ-opioid receptor agonist peptide. Inhibits electrically stimulated contraction of mouse vas deferens in vitro (EC50 = 5.2 nM), and is antinociceptive in vivo. | |||
T18725 | Sulfo-LC-SPDP | Others | |
Sulfo-LC-SPDP is a heterobifunctional crosslinker characterized by its thiol-cleavable and membrane impermeable properties. | |||
T18711 | SPDP-PEG24-acid | Others | |
SPDP-PEG24-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system w... | |||
T18716 | SPDP-PEG9-acid | Others | |
SPDP-PEG9-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system wi... | |||
T38597 | SPDP-sulfo | ||
SPDP-sulfo is a cleavable linker vital in ADC synthesis. SPDP-sulfo joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing AD... | |||
T16917 | SPDP-PEG4-NHS ester | Others | |
SPDP-PEG4-NHS ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome syst... | |||
T16916 | SPDP-PEG4-acid | Others | |
SPDP-PEG4-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system wi... | |||
T15724 | LC-PEG8-SPDP | Others | |
LC-PEG8-SPDP is a cleavable ADC linker used for the antibody-drug conjugates (ADCs)[1]. | |||
T18708 | SPDP-C6-Gly-Leu-NHS ester | Others | |
SPDP-C6-Gly-Leu-NHS ester is a cleavable linker employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T16915 | SPDP-C6-NHS ester | Others | |
SPDP-C6-NHS ester is an alkyl/ether-based linker utilized in the synthesis of PROTACs[1]. | |||
T35496 | (±)13(14)-EpDPA | ||
Cytochrome P450 metabolism of polyunsaturated fatty acids produces numerous bioactive epoxide regioisomers. (±)13(14)-EpDPA is a docosahexaenoic acid epoxygenase metabolite, derived via epoxidation of the 13,14-double bo... | |||
T35497 | (±)7(8)-EpDPA | ||
Docosahexaenoic acid is the most abundant ω-3 fatty acid in neural tissues, especially in the brain and retina. (±)7(8)-EpDPA is an epoxide derivative of DHA that is generated by the action of cytochrome P450 epoxygenase... | |||
T33904 | PDPH Crosslinker | PDPH Cross linker,SPDP Hydrazide,PDPH Cross-linker | |
PDPH crosslinker(SPDP Hydrazide) is a lytic heterobisfunctional protein crosslinker. | |||
T18525 | PC SPDP-NHS carbonate ester | Others | |
PC SPDP-NHS carbonate ester is a cleavable linker compound utilized in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T60528 | PDPOB | ||
PDPOB is a phenyl carboxylic acid derivative with the potential to be used in the study of cerebral ischemia. PDPOB is shown to be protective against OGD/R-evoked multi-aspect neuronal deterioration in SH-SY5Y cells, as ... | |||
T18710 | SPDP-PEG12-NHS ester | Others | |
SPDP-PEG12-NHS ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome sys... | |||
T36218 | 19R(20S)-EpDPA | ||
19R(20S)-EpDPA is an oxylipin and a metabolite of docosahexaenoic acid .1,2It is formed from DHA by various cytochrome P450 (CYP) isoforms in a stereoselective manner.219R(20S)-EpDPA (30 nM) prevents calcium-induced incr... | |||
T77286 | DSPE-SPDP | ||
DSPE-SPDP, a phospholipid molecule, possesses the ability to form lipid bilayers in water, making it valuable for biochemical research [1]. | |||
T18713 | SPDP-PEG36-NHS ester | Others | |
SPDP-PEG36-NHS ester is a PEG ADC linker consisting of 36 units, characterized by cleavability. It plays a crucial role in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T37238 | (±)19(20)-EpDPA | ||
EDHF (endothelium-derived hyperpolarizing factor) is an unidentified mediator released from vascular endothelial cells in response to acetylcholine and bradykinin which is distinct from the NOS- (nitric oxide) and COX-de... | |||
T37241 | (±)4(5)-EpDPA methyl ester | ||
(±)4(5)-EpDPA methyl ester is a derivative of (±)4(5)-EpDPA which is stable enough to ship and handle routinely. The active free acid can be regenerated from the methyl ester by careful base hydrolysis. (±)4(5)EpDPA is a... | |||
T14908 | CCT367766 | PROTACs | |
CCT367766 is a potent, PROTAC-based, third-generation, iso-functional pirin-targeted protein degradation probe (PDP) that depletes pirin expression at low concentrations.CCT367766 has an IC50 value of 490 nM for the CRBN... | |||
T77915 | CCT367766 formic | PROTACs | |
CCT367766 formic is a potent third-generation heterobifunctional Cereblon-based protein degradation probe (PDP, or PROTAC) that selectively targets pirin for degradation, effectively diminishing its protein expression at... |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-00714 | CD5L Protein, Mouse, Recombinant (His) | Mouse | HEK293 Cells |
CD5L Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 38 kDa and the accession number is Q9QWK4. |