Scientific Reviews
Product Guides
Blogs
Topics
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
11 Results for "
D-32
" in MedChemExpress (MCE) Product Catalog:
Products (11)
11 Results for "D-32" in MCE Product Catalog:
Cat. No.: HY-173523
CAS No.: 3054009-82-1
KI-CDK9d-32 is a selective CDK9 PROTAC degrader (IC50 = 3 nM; DC50 = 0.89 nM). KI-CDK9d-32 induces CDK9 degradation via the ubiquitin-proteasome pathway to abrogates CDK9 enzymatic and scaffolding functions, downregulates MYC expression and MYC-dependent signaling, represses TNF-alpha signaling pathways activity and pre-rRNA levels. KI-CDK9d-32 disrupts nucleolar homeostasis, blocks cell cycle progression and cellular translation by reducing 4EBP1 phosphorylation, and elicits cancer cell cytotoxicity in a CRBN-dependent manner, while high ABCB1 activity attenuates the efficacy. KI-CDK9d-32 can be used for the research of acute lymphoblastic leukemia, rhabdomyosarcoma, pancreatic adenocarcinoma .
Cat. No.: HY-101431
CAS No.: 15263-30-6
Synonyms: D32 hydrochloride
Target:
Research Areas:
Xibenolol hydrochloride (D32 hydrochloride) is an orally active beta-adrenoceptor blocking agent. Xibenolol hydrochloride can be used in the research of tachycardia and hypotension .
Cat. No.: HY-N7926S
CAS No.: 36340-20-2
Cat. No.: HY-B0712S1
Synonyms: Ro 13-9904-13C2,d32 triethylammonium salt
Cat. No.: HY-153718
CAS No.: 2416873-72-6
Research Areas:
KI-ARv-03 is a potent and selective ATP-competitive CDK9 inhibitor with an IC₅₀ of 0.15 μM (at 45 μM ATP), exhibiting over 130-fold selectivity against other CDKs (including CDK1-7). KI-ARv-03 reduces androgen receptor (AR)-driven transcription and proliferation in prostate cancer cells. KI-ARv-03 can be used for leukemia, pancreatic cancer, alveolar rhabdomyosarcoma (ARMS) and castration-resistant prostate cancer (CRPC) research. KI-ARv-03 is a ligand for target protein for PROTAC. KI-ARv-03 can be used to synthesize PROTAC KI-CDK9d-32 (HY-173523) [1][2].
Cat. No.: HY-178430S
Cat. No.: HY-163233
CAS No.: 2222120-30-9
Target:
Research Areas:
Lenalidomide 5'-piperazine can serve as a Cereblon ligand to recruit CRBN protein. Lenalidomide 5'-piperazine can be linked to target protein ligands via a linker to form PROTAC molecules, such as KI-CDK9d-32 (HY-173523) .
Cat. No.: HY-W259250S
CAS No.: 1093384-99-6
Synonyms: 2-AMino-5-chloropyridine--d3
Cat. No.: HY-W709983
Cat. No.: HY-173525
CAS No.: 3035217-26-3
Research Areas:
E3 Ligase Ligand-linker Conjugate 180 is an E3 ubiquitinase ligand-linker conjugate. E3 Ligase Ligand-linker Conjugate 180 can be used to synthesize KI-CDK9d-32 (HY-173523) .
Cat. No.: HY-P702861
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ATP6V0D1; V-Type Proton ATPase Subunit D 1; Prev. ATP6D; 32 KDa Accessory Protein; VPATPD; V-ATPase AC39 Subunit; P39; V-ATPase Subunit D 1; ATP6DV; ATPase, H+ Transporting, Lysosomal 38kDa, V0 Subunit D Isoform 1; VATX; H(+)-Transporting Two-Sector ATPas
- 1
-
-
Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
