Phenylpropanoids and polyketides
eMolecules Ambeed / 3-Bromo-4-fluorocinnamic acid / 1g / 527443839 / A579591 / / 160434-49-1 / MFCD00143095 / 245.047 / C9H6BrFO2
Ambeed / 3-Bromo-4-fluorocinnamic acid / 1g / 527443839 / A579591 / / 160434-49-1 / MFCD00143095 / 245.047 / C9H6BrFO2
eMolecules 2-(Trifluoromethyl)cinnamicacid | 2062-25-1 | MFCD00004381 | 25g
Ambeed | 2-(Trifluoromethyl)cinnamicacid | 25g | 589771508 | A698959 | | 2062-25-1 | MFCD00004381 | 216.159 | C10H7F3O2
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eMolecules 4-(4-Fluorobenzyloxy)benzaldehyde | 56442-17-2 | MFCD00173650 | 1g
Oakwood Chemical | 4-(4-Fluorobenzyloxy)benzaldehyde | 1g | 537669239 | 008325 | | 56442-17-2 | MFCD00173650 | 230.238 | C14H11FO2
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eMolecules 2'-(4-Fluorobenzyloxy)acetophenone | 400878-24-2 | MFCD03001269 | 1g
Oakwood Chemical | 2'-(4-Fluorobenzyloxy)acetophenone | 1g | 537671485 | 010106 | | 400878-24-2 | MFCD03001269 | 244.265 | C15H13FO2
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eMolecules 2-Chloro-4-hydroxycinnamic acid | 682804-97-3 | | 1g
WuXi ChemSupply | 2-Chloro-4-hydroxycinnamic acid | 1g | 599170022 | LN02190112 | 95.000 | 682804-97-3 | | 198.600 | C9H7ClO3
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eMolecules 4-(4-Fluorobenzyloxy)chlorobenzene | 332-04-7 | MFCD05105278 | 1g
Oakwood Chemical | 4-(4-Fluorobenzyloxy)chlorobenzene | 1g | 537680719 | 023259 | | 332-04-7 | MFCD05105278 | 236.670 | C13H10ClFO
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eMolecules 5-Bromo-2-methoxycinnamic acid | 40803-53-0 | MFCD00017596 | 1g
Oakwood Chemical | 5-Bromo-2-methoxycinnamic acid | 1g | 537672218 | 011098 | | 40803-53-0 | MFCD00017596 | 257.083 | C10H9BrO3
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Medchemexpress LLC (-)-Epigallocatechin Gallate | 989-51-5 | >98% | 458.37 | 1 G
(-)-Epigallocatechin Gallate (EGCG) is a major polyphenol found in green tea. It inhibits cell proliferation and induces cell apoptosis, and inhibits glutamate dehydrogenase 1/2 (GDH1/2, GLUD1/2) activity. It possesses potent anticancer, antioxidant, and anti-inflammatory properties against various types of cancers, including colorectal cancer, myeloid leukemia, and thyroid carcinoma.
- Inhibits cell proliferation
- Induces cell apoptosis
- Inhibits glutamate dehydrogenase 1/2 activity
- Possesses anticancer, antioxidant, and anti-inflammatory properties
- Effective against various cancers such as colorectal cancer, myeloid leukemia, and thyroid carcinoma
Medchemexpress LLC Xanthohumol D | 274675-25-1 | 370.40 | 1 MG
Xanthohumol D, isolated from hops, is an inhibitor of quinone reductase-2 (QR-2) with an IC50 value of 110 μM. It binds to the active site of QR-2 and shows antiproliferative activity on human cancer cell lines in vitro.
- Inhibitor of quinone reductase-2 (QR-2).
- Binds to the active site of QR-2.
- Shows antiproliferative activity on human cancer cell lines in vitro.
TARGETMOL CHEMICALS INC TANGERETIN 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Tangeretin (NSC-618905) a flavonoid from citrus fruit peels has been proven to play an important role in anti-inflammatory responses and neuroprotective effects in several disease models and was also selected as a Notch-1 inhibitor. purity: 99%
TARGETMOL CHEMICALS INC PUERARIN 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Puerarin (Kakonein) also known as Kakonein is a member of the class of compounds known as isoflavonoid C-glycosides. It is a 5-HT2C receptor antagonist. purity: 99%
Medchemexpress LLC Chlortetracycline (hydrochloride) | 64-72-2 | 95.0% | 5 G
Chlortetracycline hydrochloride is an orally active, effective, and selectively methanogenic bacteria inhibitor with bactericidal effects. It is also an antibiotic that inhibits bacterial protein synthesis. Additionally, it acts as a specific and potent calcium ionophore antibiotic by inhibiting the binding of aminoacyl-tRNA to ribosomes.
- Orally active
- Effective and selectively methanogenic bacteria inhibitor
- Bactericidal effects
- Inhibits bacterial protein synthesis
- Specific and potent calcium ionophore antibiotic
- Inhibits binding of aminoacyl-tRNA to ribosomes
Medchemexpress LLC PI3K/AKT-IN-1 | 3033069-84-7 | 99.6% | C23H23N5O4S | 25 MG
PI3K/AKT-IN-1 is an effective dual inhibitor of PI3K and AKT, exhibiting anticancer activity by inhibiting the PI3K/AKT axis and inducing caspase 3-dependent apoptosis. This compound has high cytotoxic activity against leukemia K562 and breast cancer MCF-7 cell lines, and is intended for research use only.
- Demonstrates high cytotoxic activity, particularly against leukemia cell line K562 (IC50=2.62 μM) and breast cancer cell line MCF-7 (IC50=3.22 μM)
- Promotes S-phase cell cycle arrest and induces apoptosis in K562 cells
- Significantly reduces the expression of PI3K, p-PI3K, AKT, p-AKT, Cyclin D1, and NF-κB
- Found to be non-toxic and well-tolerated in animal studies, with an LD50 greater than 2000 mg/kg
- Soluble in DMSO at 50 mg/mL
- Solid, off-white to light yellow appearance
Medchemexpress LLC Xanthohumol | 6754-58-1 | 354.40 | 100 MG
Xanthohumol | 6754-58-1 | 354.40 | 100 MG
TARGETMOL CHEMICALS INC AKT-I-1 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. AKT-I-1 is a selective and reversible inhibitor of Akt1. purity: 98%