| DC72448 |
Tallimustine |
Tallimustine (FCE 24517), a distamycin-A derivative, is an anticancer agent. |
|
| DC72449 |
MRV03-069 |
MRV03-069 (Compound 3) is a selective colibactin-activated peptidase (ClbP) inhibitor that blocks the genotoxic effect of Colibactin on eukaryotic cells. MRV03-069 can be used in colorectal cancer research. |
|
| DC72450 |
Prohexadione calcium |
Prohexadione (BX-112) calcium is a plant growth regulator. Prohexadione inhibits gibberellin biosynthesis of plants. |
|
| DC72451 |
PBT 1033
Featured
|
PBT 1033 (PBT 2) is an orally active copper/zinc ionophore. PBT 1033 restores cognition in mouse models of Alzheimer's disease (AD). PB 1033 also has antibacterial activity against Gram-positive bacteria. |
|
| DC72452 |
Prohexadione |
Prohexadione (BX-112 free acid) is a plant growth regulator. Prohexadione inhibits gibberellin biosynthesis of plants. |
|
| DC72453 |
ZINC00784494 |
ZINC00784494 is a specific Lipocalin-2 (LCN2) inhibitor. ZINC00784494 inhibits cell proliferation, cell viability and reduces AKT phosphorylation levels in SUM149 cells. ZINC00784494 has good potential for research in inflammatory breast cancer (IBC). |
|
| DC72454 |
ZINC00640089
Featured
|
ZINC00640089 is a specific Lipocalin-2 (LCN2) inhibitor. ZINC00640089 inhibits cell proliferation, cell viability and reduces AKT phosphorylation levels in SUM149 cells. ZINC00640089 has good potential for research in inflammatory breast cancer (IBC). |
|
| DC72455 |
MS47134 |
MS47134 is a potent and selective MRGPRX4 agonist with an EC50 value of 149 nM. MS47134 can be used for research of pain, itch and mast cell-mediated hypersensitivity. |
|
| DC72456 |
(+)SHIN2 |
(+)SHIN2 is a serine hydroxymethyltransferase (SHMT) inhibitor, whose target can be traced with 13C-serine. (+)SHIN2 increases survival in NOTCH1-driven mouse primary acute lymphoblastic leukemia (T-ALL) in vivo with a synergistic effect with Methotrexate. |
|
| DC72457 |
PTB7-Th |
PTB7-Th is a classic organic photovoltaic (OPV) cell donor polymer that can be added as a dielectric to increase the short-circuit current and fill factor of polymer solar cells, improving the photovoltaic efficiency of the device. |
|
| DC72458 |
4-Formylcolchicine |
4-Formylcolchicine is a potent anticancer agent. 4-Formylcolchicine shows cytotoxicity activity with IC50 values of 1.007, 0.128, 0.054 µM for A549, HT-29, HCT116 cells, respectively. |
|
| DC72459 |
LSTc |
LSTc (LS-tetrasaccharide c) is a human lactooligosaccharide presents on glycoproteins and glycolipids. LSTc is also a specific human JC polyomavirus (JCV) recognition motif. LSTc has good potential for the study of progressive multifocal leukoencephalopathy (PML). |
|
| DC72460 |
SRI 6409-94
Featured
|
SRI 6409-94 is an orally active Ro 13-6298 analogue that is teratogenic. SRI 6409-94 serves as a molecular tool to study the effect of the three-dimensional configuration of retinol on teratogenic activity. |
|
| DC72461 |
Dihydrokalafungin |
Dihydrokalafungin (Antibiotic YS-02931K-β) is a benzoisochromanequinone that used as a natural substrate in enzyme assays of the ActVB-ActVA system. |
|
| DC72462 |
JA-ACC |
JA-ACC (Jasmonyl-ACC) is a derivative of 1-aminocyclopropane-1-carboxylic acid (ACC). is ACC is the direct precursor of the plant hormone ethylene. JA-ACC inhibits root growth in Arabidopsis and the inhibition is independent of jasmonic acid (JA) signaling. |
|
| DC72463 |
L1-PEG2-TATE |
L1-PEG2-TATE is a nonadentate ligand. L1-PEG2-TATE can be used for the research of imaging. |
|
| DC72464 |
NCGC00138783 free base |
NCGC00138783 free base is a selective inhibitor targeting CD47/SIRPα axis, with an IC50 of 50 µM. NCGC00138783 free base directly blocks the interaction between CD47 and SIRPα axis. |
|
| DC72465 |
(R)-PF-04991532 |
(R)-PF-04991532 is the R-enantiomer of PF-04991532. PF-04991532 is a potent, hepatoselective glucokinase activator. |
|
| DC72466 |
H-Cys-Val-2-Nal-Met-OH |
H-Cys-Val-2-Nal-Met-OH is a peptide. H-Cys-Val-2-Nal-Met-OH is a peptidomimetic derivative that can be used to label short peptide sequences. |
|
| DC72467 |
5-Oxoprolyltryptophan |
5-Oxoprolyltryptophan is a model substrate for investigating the increase of serotonin at the cerebral level. |
|
| DC72468 |
DBCO-PEG2-NHS ester |
DBCO-PEG2-NHS ester is a click chemistry reagent containing an azide group. DBCO-PEG2-NHS ester is a click chemistry PEG reagent containing NHS ester that is able to react specifically and efficiently with primary amines (e.g. the side chain of lysine residues or aminosilane-coated surfaces) at neutral or slightly basic condition to form a covalent bond. The hydrophilic PEG spacer arm improves water solubility and provides a long and flexible connection that minimizes steric hindrance involved with ligation. DBCO is commonly used for copper-free Click Chemistry reactions. Reagent grade, for research use only. |
|
| DC72469 |
Fmoc-EDA-N3 |
Fmoc-EDA-N3 is a click chemistry reagent containing an azide group. |
|
| DC72470 |
Glp-Trp-OEt |
Glp-Trp-OEt, a pyroglutamyl-tryptophan derivative, is a dipeptide Et ester. |
|
| DC72471 |
Sialylglyco peptide |
Sialylglyco peptide is a N-Glycan and sialate glycopeptide. |
|
| DC72472 |
OSu-PEG4-VC-PAB-MMAE |
OSu-PEG4-VC-PAB-MMAE involves in GDP-FAmP4MMAE (Monomethylauristatin E) synthesis, which is for GDP label via site-specific conjugation. |
|
| DC72473 |
2'-O-MB-cAMP sodium |
2'-O-MB-cAMP (2'-O-Monobutyryl cyclic AM) sodium is an activatable prodrug of Cyclic AMP. |
|
| DC72474 |
Asobamast |
Asobamast is a potent, orally active antiallergic agent that inhibits ige mediated passive pulmonary allergic responses in rats (ED50=4.7 mg/kg) and inhibits antigen-induced mediator release from sensitized guinea pig lung fragments. |
|
| DC72475 |
G0 N-glycan-Asn |
G0 N-glycan-Asn is a glycopeptide. G0 N-glycan-Asn can be used for various biochemical studies. |
|
| DC72476 |
Indole-C2-amide-C2-NH2 |
Indole-C2-amide-C2-NH2 is a potent linker. |
|
| DC72477 |
L-Tryptophanylglycine |
L-Tryptophanylglycine (Trp-gly) is a dipeptide that can inhibit Ceronapril uptake by Caco-2 cells, with a Ki of 7.19 mM. |
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