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Filtered Search Results
Aobchem 4-Chloro- -ethyl-2-fluorobenzenemethanol | ≥95% | CAS 1427380-66-2 | C9H10ClFO | 500mg
4-Chloro- -ethyl-2-fluorobenzenemethanol | ≥95% | CAS 1427380-66-2 | C9H10ClFO | 500mg
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Medchemexpress LLC 2-chloro-6-fluorobenzaldehyde | 387-45-1 | MFCD00003306 | 99.7% | 158.56 g/mol | C7H4ClFO | 1 KG
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2-Chloro-6-fluorobenzaldehyde is an aromatic aldehyde used as a synthetic building block in organic chemistry and research. It is employed in condensation reactions and other transformations to introduce a 2-chloro-6-fluorophenyl-CHO motif; consult the batch COA for exact specifications.
- High reported purity; verify batch COA for exact value.
- Available in multiple sizes including kilo-scale for scale-up work.
- Supplied with certificate of analysis and safety data sheet.
- Solid at ambient temperatures below ~32°C; may liquefy above ~35°C.
- Useful building block for pharmaceutical and agrochemical synthesis.
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Selleck Chemical LLC NPS-1034 5mg 1221713-92-3
NPS-1034 is a dual Met (c-Met)/Axl inhibitor with IC50 of 48 nM and 10.3 nM, respectively. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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Medchemexpress LLC HY-N1984 5mg Medchemexpress, Artemisic acid CAS:80286-58-4 Purity:>98%
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Medchemexpress, HY-N1984 5mg Artemisic acid CAS:80286-58-4 Artemisinic acid (Qing Hao acid), an amorphane sesquiterpene isolated from Artemisia annua L., possesses a variety of pharmacological activity, such as antimalarial activity, anti-tumor activity, antipyretic effect, antibacterial activity, allelopathy effect and anti-adipogenesis effect. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Aobchem 1-Bromo-3 4-difluorobenzene | ≥97% | CAS 348-61-8 | C6H3BrF2 | 100g
1-Bromo-3 4-difluorobenzene | ≥97% | CAS 348-61-8 | C6H3BrF2 | 100g
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Medchemexpress LLC HY-128378 50mg Medchemexpress, 16-Dehydroprogesterone CAS:1096-38-4 Purity:>98%
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Medchemexpress, HY-128378 50mg 16-Dehydroprogesterone CAS:1096-38-4 16-Dehydroprogesterone is a steroidal progestin. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Rieke Metals LLC 2,5-DIFLUOROBENZYL MG BR
2,5-Difluorobenzylmagnesium bromide, 0.25M diethyl ether
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eMolecules 1200-27-7 | 1-(4-Fluorophenyl)-2-methyl-2-propylamine | Activate Scientific | MFCD00075463 | 203.690 | C10H15ClFN | 98.000 | Cl.CC(C)(N)Cc1ccc(F)cc1 | 5g | 602845118
1-(4-Fluorophenyl)-2-methyl-2-propylamine | Activate Scientific | 1200-27-7 | MFCD00075463 | 203.690 | C10H15ClFN | 98.000 | Cl.CC(C)(N)Cc1ccc(F)cc1 | 5g | 602845118
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Selleck Chemical LLC R547 S2688-2mg
R547 (Ro 4584820) is a potent ATP-competitive inhibitor of CDK1/2/4 with Ki of 2 nM/3 nM/1 nM It is less potent to CDK7 and GSK3 / while inactive to other kinases Phase 1
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Selleck Chemical LLC Encorafenib
Encorafenib is a highly potent RAF inhibitor with selective anti-proliferative and apoptotic activity in cells expressing B-RAF(V600E) with EC50 of 4 nM Phase 3
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Medchemexpress LLC HY-111420 5mg Medchemexpress, CBP/EP300-IN-1 CAS: Purity:>98%
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Medchemexpress, HY-111420 5mg CBP/EP300-IN-1 CAS: CBP/EP300-IN-1 is a CBP/EP300 bromodomain inhibitor. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC 4-Chloro-2-fluoroben | 10G
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4-Chloro-2-fluoroben | 10G
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Selleck Chemical LLC ASP5878
ASP5878 is a novel FGFR-selective inhibitor with IC50 values of 0 47 0 60 0 74 and 3 5 nmol/L for recombinant FGFR1 2 3 and 4 respectively
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Medchemexpress LLC Not found on product page (SDS link not accessible) | 2607138-82-7 | MFCD34602688; MFCD33402167 | 99.9% | 461.79 | C19H16ClF4N3O4 | 5 MG
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ART812 is a small-molecule, orally active inhibitor of DNA polymerase theta (Polθ) with high biochemical potency (Polθ IC50 ~7.6 nM). It exhibits cellular activity in microhomology-mediated end joining (MMEJ) assays (IC50 ~240 nM) and has been investigated preclinically for targeting homologous recombination-deficient tumors and for overcoming PARP inhibitor resistance.
- High biochemical potency: Polθ IC50 ~7.6 nM
- Cellular activity in MMEJ assays (IC50 ~240 nM)
- Orally active small molecule suitable for in vivo studies
- Mechanism targets Polθ-mediated DNA repair pathways
- Investigated for synthetic-lethal targeting of HR-deficient tumors
- High reported purity (~99.9%) for research use
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Medchemexpress LLC NaV1.7 inhibitor-1 | 1494585-79-3 | 99.2% | 100 MG
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NaV1.7 inhibitor-1 is a potent research-grade small molecule inhibitor of the voltage-gated sodium channel NaV1.7, reported with sub-nanomolar potency in cellular assays. Supplied as a high-purity solid, it is intended for in vitro pharmacology and electrophysiology studies and is for research use only.
- High potency against human NaV1.7 (IC50 = 0.6 nM).
- Selective over NaV1.5 (~80-fold selectivity).
- High purity (99.17% by LCMS).
- Available in multiple pack sizes, including 100 MG solid and 10 mM DMSO solutions.
- Molecular formula C23H30FNO4S, molecular weight ~435.6 g/mol.
- Intended for laboratory research use only.
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