64640-77-3
64640-77-3
Chemical Structure
SD-066-4
- CAS No.: 64640-77-3
- Formula:C18H15N3
- Molecular Weight:273.33
InChIKey: XJUJNQLHZRQSNB-UHFFFAOYSA-N
SMILES: CC(C=C1)=CC=C1C2=CC(C3=CNC4=CC=CC=C43)=NN2
Biological Activity: SD-066-4 is an orally active acyltransferase inhibitor. SD-066-4 can be used in cancer research[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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SD-066-4 | 99.96% | SD-066-4 is an orally active acyltransferase inhibitor. SD-066-4 can be used in cancer research. | ||||||||||||||||||||
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3-(4-Pyridyl)indole | 99.94% | 3-(4-Pyridyl)indole (Rockout; 3-(4-Pyridinyl)-1H-indole; Rho Kinase Inhibitor III, Rockout) is a Rho-kinase inhibitor (IC50 = 25 μM). 3-(4-Pyridyl)indole inhibits cell migration, membrane blebbing, and stress fiber and focal adhesion formation, and induces actin stress fiber disassembly. 3-(4-Pyridyl)indole promotes cell spreading and alters cell morphology and dynamics. 3-(4-Pyridyl)indole inhibits PRK2. 3-(4-Pyridyl)indole is used in wound healing research. | ||||||||||||||||||||
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VRT-532 | 98.98% | VRT-532 (CFpot-532) is a potent is a potent CFTR modulator. VRT-532 enhances channel activity in G551D-CFTR and intrinsic ATPase activity of G551D-CFTR. VRT-532 has the potential for the research of cystic fibrosis. | ||||||||||||||||||||
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VPC-13566 | 99.92% | VPC-13566, a BF3-specific small molecule, is an androgen receptor (AR) inhibitor. VPC-13566 is effective in inhibiting AR transcriptional activity in vitro as well as the growth of AR-dependent PCa cell lines. VPC-13566 can be used as a chemical probe to help identify unknown AR partners.VPC-13566 can be used for the research of cancer. | ||||||||||||||||||||
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Antibacterial agent 82 | Antibacterial agent 82 (compound 7p) is an antibacterial agent. | |||||||||||||||||||||
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QR-0217 | 98.47% | QR-0217 is a potent Aβ1-40 aggregation inhibitor with an IC50 value of 7.5 µM. QR-0217 inhibits α-synuclein aggregation. QR-0217 reduces memory impairments caused by Aβ neurotoxicity. | ||||||||||||||||||||
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VEGFR-2-IN-65 | VEGFR-2-IN-65 (Compound 07) is a VEGFR-2 inhibitor. VEGFR-2-IN-65 has H-bond interactions with Cys180. VEGFR-2-IN-65 inhibits tube formation in HUVECs. | |||||||||||||||||||||
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MLS000099089 | MLS000099089 is a 12/15-lipoxygenase (12/15-LOX) inhibitor with IC50 values of 3.4 μM and 10 μM for human and mice 12/15-LOX, respectively. MLS000099089 displays higher selectivity for 12/15-LOX over 5-LOX and COX-2. MLS000099089 can be used for the study of stroke. | |||||||||||||||||||||
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3-Phenylindole | 3-Phenylindole (3-phenyl-1H-indole) is an indole compound. 3-Phenylindole exhibits weak anti-tuberculosis activity with an MIC of 129.4 μM. 3-Phenylindole can be utilized in anti-tuberculosis research. | |||||||||||||||||||||
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3-(5-(Pyridin-4-yl)-1H-pyrazol-3-yl)pyridine | 3-(5-(Pyridin-4-yl)-1H-pyrazol-3-yl)pyridine is a metal-organic framework (MOF). | |||||||||||||||||||||
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3,3'-Bi[1H-indole] | 3,3'-Bi[1H-indole] is a MtbFtsZ inhibitor. 3,3'-Bi[1H-indole] inhibits the GTPase activity of MtbFtsZ. 3,3'-Bi[1H-indole] increases the cell length of Mycobacterium smegmatis and Bacillus subtilis. 3,3'-Bi[1H-indole] can be used in the research of tuberculosis. | |||||||||||||||||||||
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