Halophenols
- (144)
- (5)
- (41)
- (1)
- (3)
- (4)
- (90)
- (1)
- (12)
- (4)
- (2)
- (1)
- (2)
- (1)
- (1)
- (190)
- (1)
- (3)
- (8)
- (22)
- (1)
- (20)
- (2)
- (1)
- (204)
- (1)
- (3)
- (1)
- (21)
- (3)
- (6)
- (49)
- (1)
- (2)
- (1)
- (2)
- (2)
- (1)
- (2)
- (1)
- (1)
- (5)
- (14)
- (4)
- (1)
- (2)
- (1)
- (2)
- (1)
- (16)
- (2)
- (11)
- (26)
- (2)
- (16)
- (6)
- (1)
- (2)
- (2)
- (1)
- (3)
- (2)
- (1)
- (5)
- (2)
- (1)
- (8)
- (1)
- (1)
- (1)
- (18)
- (1)
- (3)
- (1)
- (1)
- (2)
- (1)
- (7)
- (11)
- (4)
- (5)
- (2)
- (2)
- (1)
- (1)
- (1)
- (4)
- (2)
- (4)
- (1)
- (4)
- (6)
- (1)
- (3)
- (1)
- (1)
- (23)
- (4)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (4)
- (3)
- (30)
- (3)
- (4)
- (1)
- (1)
- (1)
- (1)
- (4)
- (1)
- (10)
- (15)
- (14)
- (12)
- (9)
- (4)
- (1)
- (1)
- (4)
- (1)
- (1)
- (1)
- (1)
- (4)
- (3)
- (2)
- (1)
- (2)
- (2)
- (1)
- (3)
- (8)
- (3)
- (1)
- (2)
- (1)
- (2)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (23)
- (5)
- (2)
- (2)
- (2)
- (1)
- (2)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (7)
- (2)
- (2)
- (1)
- (4)
- (5)
- (1)
- (13)
- (3)
- (1)
- (1)
- (1)
- (13)
- (5)
- (1)
- (4)
- (17)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (3)
- (2)
- (4)
- (6)
- (2)
- (5)
- (22)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (6)
- (3)
- (2)
- (2)
- (2)
- (2)
- (3)
- (1)
- (2)
- (1)
- (2)
- (6)
- (1)
- (1)
- (1)
- (1)
- (2)
- (4)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (9)
- (6)
- (3)
- (2)
- (1)
- (2)
- (2)
- (5)
- (2)
- (2)
- (4)
- (1)
- (1)
- (1)
- (2)
- (1)
- (2)
- (6)
- (1)
- (3)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (2)
- (5)
- (2)
- (1)
- (2)
- (2)
- (3)
- (2)
- (1)
- (1)
- (1)
- (2)
- (7)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (1)
- (5)
- (1)
- (2)
- (1)
- (3)
- (1)
- (4)
- (1)
- (1)
- (5)
- (2)
- (1)
- (3)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (6)
- (1)
- (2)
- (1)
- (1)
- (11)
- (2)
- (1)
- (1)
- (10)
- (11)
- (9)
- (1)
- (2)
- (1)
- (41)
- (75)
- (110)
- (2)
- (1)
- (4)
- (9)
- (2)
- (5)
- (7)
- (7)
- (2)
- (3)
- (2)
- (1)
- (3)
- (2)
- (1)
- (15)
- (2)
- (5)
- (18)
- (92)
- (181)
- (5)
- (86)
- (7)
- (1)
- (3)
- (6)
- (19)
- (2)
- (1)
- (215)
- (3)
- (8)
- (5)
- (2)
- (2)
- (2)
- (11)
- (6)
- (2)
- (47)
- (4)
- (3)
- (3)
- (2)
- (22)
- (1)
- (2)
- (22)
- (2)
- (2)
- (2)
- (3)
- (3)
- (1)
- (2)
- (2)
- (2)
- (1)
- (4)
- (2)
- (3)
- (1)
- (3)
- (1)
- (2)
- (3)
- (2)
- (2)
- (1)
- (4)
- (3)
- (4)
- (2)
- (2)
- (11)
- (1)
- (5)
- (2)
- (2)
- (2)
- (2)
- (5)
- (1)
- (1)
- (2)
- (1)
- (2)
- (1)
- (5)
- (2)
- (2)
- (3)
- (6)
- (2)
- (2)
- (2)
- (3)
- (2)
- (2)
- (2)
- (3)
- (2)
- (5)
- (3)
- (4)
- (2)
- (1)
- (3)
- (2)
- (3)
- (6)
- (2)
- (3)
- (5)
- (4)
- (4)
- (3)
- (1)
- (6)
- (4)
- (3)
- (2)
- (3)
- (2)
- (4)
- (2)
- (2)
- (2)
- (6)
- (5)
- (4)
- (6)
- (3)
- (3)
- (3)
- (5)
- (5)
- (2)
- (1)
- (2)
- (2)
- (3)
- (2)
- (2)
- (2)
- (1)
- (2)
- (3)
- (2)
- (3)
- (2)
- (2)
- (2)
- (4)
- (1)
- (2)
- (2)
- (2)
- (2)
- (3)
- (2)
- (2)
- (2)
- (2)
- (2)
- (2)
- (4)
- (2)
- (1)
- (1)
- (2)
- (3)
- (2)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (3)
- (2)
- (1)
- (3)
- (2)
- (3)
- (2)
- (1)
- (2)
- (3)
- (1)
Filtered Search Results
Medchemexpress LLC MGCD-265 analog | 875337-44-3 | 98.57% | 517.60 | 1 ML
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
MGCD-265 analog is a potent and oral active inhibitor of c-Met and VEGFR2 tyrosine kinases, with IC50s of 29 nM and 10 nM, respectively, and has significant antitumor activity.
- Potent inhibitor of c-Met and VEGFR2 tyrosine kinases.
- Oral active.
- Exhibits significant antitumor activity.
- Inhibits A549 cells migration and DU145 cells scattering.
- Inhibits HUVEC ERK phosphorylation and HUVEC proliferation.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC GSK 1562590 (hydrochloride) | 1003878-07-6 | 99.0% | 617.95 | 50 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
GSK 1562590 hydrochloride is a high affinity and selective antagonist of urotensin-II receptor (UT), with pKis of 9.14-9.66 for mammalian recombinant (mouse, rat, cat, monkey, human) and native UT.
- High affinity and selective antagonist of urotensin-II receptor (UT).
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC SB-772077B dihydrochloride | 607373-46-6 | 99.3% | 415.28 | 1 ML
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
SB-772077B dihydrochloride is an orally active aminofuran-based Rho kinase inhibitor, with IC50 values of 5.6 nM and 6 nM for ROCK1 and ROCK2, respectively. It reduces inflammatory cytokines such as TNF-α and IL-6. This compound also relaxes aortic rings and lowers blood pressure. It can be utilized in the research of inflammatory diseases.
- Orally active.
- Reduces inflammatory cytokines.
- Relaxes aortic rings.
- Lowers blood pressure.
- Useful in inflammatory disease research.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Aobchem 3-Chloro-2-fluorobenzaldehyde | ≥97% | CAS 85070-48-0 | C7H4ClFO | 100g
3-Chloro-2-fluorobenzaldehyde | ≥97% | CAS 85070-48-0 | C7H4ClFO | 100g
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC AZD 6482 | 1173900-33-8 | 99.9% | 408.45 | 25 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
AZD 6482 | 1173900-33-8 | 99.9% | 408.45 | 25 MG
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC AZ10606120 dihydrochloride | 607378-18-7 | 99.93% | 495.48 | 25 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
AZ10606120 dihydrochloride is a selective, high affinity antagonist for the P2X7 receptor (P2X7R) at human and rat with an IC50 of about 10 nM. It exhibits minimal or no effect at other P2XR subtypes and has demonstrated anti-depressant effects and the ability to reduce tumor growth.
- Selective and high-affinity antagonist for P2X7 receptor.
- Little or no effect on other P2XR subtypes.
- Shows anti-depressant effects.
- Reduces tumor growth.
- Depletes tumor cells in patient-derived primary glioblastoma samples.
- Increases Lactate dehydrogenase (LDH) levels in human primary glioblastoma cultures.
- Reduces proliferation, cell migration, and invasion in PDAC cell lines.
- Reverses Streptozotocin-induced VEGF and IL-6 expression in rat retinae.
- Exhibits antidepressant phenotype in LPS-induced anhedonia mice.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC SB-772077B (dihydrochloride) | 607373-46-6 | 99.33% | 415.28 | 25 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
SB-772077B dihydrochloride is an orally active aminofuran-based Rho kinase (ROCK) inhibitor. It has IC50 values of 5.6 nM for ROCK1 and 6 nM for ROCK2, reduces inflammatory cytokines, relaxes aortic rings, and lowers blood pressure. It is used in inflammatory disease research.
- Reduces LPS-induced inflammatory cytokines (TNF-α and IL-6) in primary human macrophages.
- Induces dose-dependent relaxation of Phenylephrine-precontracted rat aortic rings (IC50 of 39 nM).
- Significantly reduces blood pressure in spontaneously hypertensive and deoxycorticosterone acetate-induced hypertensive rats.
- Abolishes Angiotensin II-induced actin stress fiber formation in human primary aortic smooth muscle cells at 3 μM.
- Intended for research use only.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC 4'-(Imidazol-1-yl) acetophenone | 10041-06-2 | 99.9% | 186.21 | 25 G
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
The product is a selective thromboxane synthetase inhibitor. It is also known by its synonym, (4'-(Imidazol-1-yl) acetophenone).
- Provided as a solid, white to off-white in appearance.
- High purity, typically 99.91%.
- Stable for 3 years at room temperature in continental US.
- Can be stored in solvent for 2 years at -80°C and 1 year at -20°C.
- Available in various quantities, from 5 g to 50 g.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC Parsaclisib hydrochloride | 1995889-48-9 | 99.3% | 469.34 | 25 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Parsaclisib hydrochloride is a potent, selective, and orally active inhibitor of PI3Kδ, with an IC50 of 1 nM at 1 mM ATP. It exhibits approximately 20000-fold selectivity over other PI3K class I isoforms. It is used for the research of relapsed or refractory B-cell malignancies.
- Potent, selective, and orally active PI3Kδ inhibitor
- Exhibits approximately 20000-fold selectivity over other PI3K class I isoforms
- Inhibits proliferation of MCL and DLBCL cell lines
- Inhibits anti-IgM-induced pAKT (Ser473) in Ramos Burkitt's lymphoma cell line
- Inhibits proliferation of human, dog, rat, and mouse primary B cells
- Inhibits tumor growth in BALB/c mice bearing A20 murine lymphoma cells
- Slows Pfeiffer xenograft tumor growth in a dose-dependent manner
- Reduces percentage of Tregs (CD4+CD25+FOXP3+) in tumors and spleens
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC NH-bis PEG2-propargy | 50MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
NH-bis PEG2-propargy | 50MG
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC (S)-UFR2709 hydrochloride | 2934318-93-9 | 98.1% | 255.74 | 1 ML
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
(S)-UFR2709 (hydrochloride) is a competitive nAChR antagonist that shows higher affinity for α4β2 nAChRs than for α7 nAChRs. It has been observed to decrease anxiety and reduce ethanol consumption and preference in alcohol-preferring rats. (S)-UFR2709 (hydrochloride) acts as an anxiolytic agent and can be utilized in the study of nicotine addiction.
- Competitive nAChR antagonist
- Shows higher affinity for α4β2 nAChRs than for α7 nAChRs
- Decreases anxiety and reduces ethanol consumption
- Utilized in the study of nicotine addiction
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC Avotaciclib hydrochloride | 1983983-41-0 | 99.75% | 317.73 | 100 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Avotaciclib hydrochloride (Synonyms: BEY1107 hydrochloride) is an orally active cyclin-dependent kinase 1 (CDK1) inhibitor. It can inhibit the proliferation and induce apoptosis of tumor cells, making it suitable for cancer research, including pancreatic cancer and lung cancer.
- Orally active CDK1 inhibitor.
- Inhibits proliferation of tumor cells.
- Induces apoptosis in tumor cells.
- Applicable in research for various cancers like pancreatic cancer and lung cancer.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC Icapamespib hydrochloride | 2267287-26-1 | 98.74% | 599.32 | 100 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Icapamespib hydrochloride | 2267287-26-1 | 98.74% | 599.32 | 100 MG
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC Avotaciclib hydrochloride | 1983983-41-0 | 99.75% | 317.73 | 50 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Avotaciclib hydrochloride is an orally active cyclin-dependent kinase 1 (CDK1) inhibitor. It inhibits the proliferation and induces apoptosis of tumor cells, and can be used in the research of cancers such as pancreatic cancer and lung cancer. This potent compound targets CDK1 activity, which may inhibit cancer stem cell division, lead to cell cycle arrest, and induce apoptosis, thereby inhibiting tumor cell proliferation.
- Orally active CDK1 inhibitor
- Inhibits proliferation and induces apoptosis of tumor cells
- Useful in research for cancers such as pancreatic cancer and lung cancer
- Targets and inhibits CDK1 activity
- May inhibit cancer stem cell division
- Leads to cell cycle arrest
- Induces apoptosis
- Potential antitumor activity
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Medchemexpress LLC Bis-PEG23-endo-BCN | ≥98.0% | 1425.73 | 25 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Small and/or specialty supplier based on Federal laws and SBA requirements.
Learn More
Bis-PEG23-endo-BCN is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent, featuring a BCN group capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing azide groups.
- PEG-based PROTAC linker
- Used for synthesis of PROTACs
- Click chemistry reagent
- Features a BCN group
- Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC)
- For research use only
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More