Unsubstituted Phenols
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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences PhenolChloroformIso-amyl
PhenolChloroformIso-amyl alcohol (125241) is used for the purification of total RNA from mixtures of crude cell extracts and can eliminate the need for a time consuming ultracentrifugation step.
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MEDCHEMEXPRESS LLC GENISTEIN 100MG
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501873053 GENISTEIN 100MG
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MEDCHEMEXPRESS LLC ISOGINKGETIN 5MG
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501874639 ISOGINKGETIN 5MG
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Apexbio Technology LLC L-690,330 142523-38-4 10mg
L-690 330 (CAS 142523-38-4) is a competitive inhibitor of inositol monophosphatase (IMPase) exhibiting a Ki between 0 2 and 2 M depending on the enzyme source IMPase catalyzes the hydrolysis of inositol monophosphates yielding free inositol for phosphatidylinositol (PI) cycle signaling In M1 CHO cells L-690 330 did not elevate [3H]InsP1 levels alone but attenuated carbachol-stimulated increases producing effects up to 40% of those observed with lithium In vivo L-690 330 administration led to significant Ins(1)P accumulation in mouse brain following muscarinic agonist stimulation These properties make L-690 330 a valuable tool for probing inositol signaling pathways and studying IMPase-related neurological processes
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Medchemexpress LLC Procyanidin B3 | 23567-23-9 | 5 MG
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Procyanidin B3 is a natural product that exhibits antioxidant activity and oral bioavailability. It has good blood-brain barrier penetration and acts as a selective inhibitor of histone acetyltransferase (HAT). It inhibits p300 HAT-mediated acetylation of the androgen receptor and can alleviate intervertebral disc degeneration (IVDD) by inhibiting the formation of the TLR4/MD-2 complex. Procyanidin B3 is suitable for research related to prostate cancer and arthritis.
- Natural product
- Antioxidant activity
- Oral bioavailability
- Good blood-brain barrier penetration
- Selective inhibitor of histone acetyltransferase (HAT)
- Inhibits p300 HAT-mediated acetylation of the androgen receptor
- Alleviates intervertebral disc degeneration (IVDD) by inhibiting the formation of the TLR4/MD-2 complex
- Can be used in research on prostate cancer and arthritis
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Medchemexpress LLC HY-16950 50mg , 4-Hydroxytamoxifen (Z)-4-Hydroxytamoxifen;trans-4-Hydroxytamoxifen CAS:68047-06-3 Purity:98%
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Medchemexpress, HY-16950 50mg 4-Hydroxytamoxifen (Z)-4-Hydroxytamoxifen;trans-4-Hydroxytamoxifen CAS:68047-06-3 Formula:C26H29NO2 IC50: 3.3 nM (Oestrogen receptor) CRISPR/Cas9 Purity:98% 4-Hydroxytamoxifen, an active metabolite of tamoxifen, is a selective estrogen receptor antagonist, with an IC 50 of 3.3 nM for the [ 3 H]oestradiol binding to oestrogen receptor, widely used to treat breast cancer; 4-Hydroxytamoxifen also increases CRISPR/Cas9 -mediated editing frequency. 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 HY-16561 500mg , Resveratrol trans-Resveratrol CAS:501-36-0 Purity:98%
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Medchemexpress, HY-16561 500mg Resveratrol trans-Resveratrol CAS:501-36-0 Formula:C14H12O3 IC50: 0.8 μM (Adenylyl cyclase), 1 μM (IKKβ), 3.3 and 5 μM (DNA polymerase α and δ) Purity:98% Resveratrol is one of the numerous polyphenolic compounds found in several vegetal sources, has a wide spectrum of targets with IC 50 of 0.8, 1, 3.3 and 5 μM for adenylyl cyclase, IKKβ , DNA polymerase α and δ, respectively. 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 (-)-Catechin | 18829-70-4 | 290.27 | 50 MG
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(-)-Catechin is a structural variation of Catechin. It acts as an inhibitor of enzyme-1 (COX-1) with an IC50 of 1.4 μM. Additionally, (-)-Catechin promotes the differentiation of hBM-MSC adipose cells, leading to increased fat cell differentiation and elevated PPARγ levels.
- Catechin's one kind of different structure.
- Inhibits COX-1 with an IC50 of 1.4 μM.
- Promotes hBM-MSC adipose cell differentiation.
- Increases fat cell differentiation.
- Increases PPARγ level.
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Aobchem 2-(Phenoxymethyl)phenol | 95% | CAS 76176-97-1 | C13H12O2 | 250mg
2-(Phenoxymethyl)phenol | 95% | CAS 76176-97-1 | C13H12O2 | 250mg
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Aobchem Phenol 2 3 4 5 6-pentafluoro- 1-methanesulfonate | 95% | CAS 161912-36-3 | C7H3F5O3S | 5g
Phenol 2 3 4 5 6-pentafluoro- 1-methanesulfonate | 95% | CAS 161912-36-3 | C7H3F5O3S | 5g
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Aobchem Phenol 2 3 4 5 6-pentafluoro- 1-methanesulfonate | 95% | CAS 161912-36-3 | C7H3F5O3S | 250mg
Phenol 2 3 4 5 6-pentafluoro- 1-methanesulfonate | 95% | CAS 161912-36-3 | C7H3F5O3S | 250mg
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Aobchem Phenol 2 3 4 5 6-pentafluoro- 1-methanesulfonate | 95% | CAS 161912-36-3 | C7H3F5O3S | 25g
Phenol 2 3 4 5 6-pentafluoro- 1-methanesulfonate | 95% | CAS 161912-36-3 | C7H3F5O3S | 25g
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Aobchem Phenol 5-bromo-2-methyl- 1-acetate | 95% | CAS 86297-38-3 | C9H9BrO2 | 5g
Phenol 5-bromo-2-methyl- 1-acetate | 95% | CAS 86297-38-3 | C9H9BrO2 | 5g
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Aobchem 2-(Phenoxymethyl)phenol | 95% | CAS 76176-97-1 | C13H12O2 | 10g
2-(Phenoxymethyl)phenol | 95% | CAS 76176-97-1 | C13H12O2 | 10g
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Aobchem 2-Bromo-4-(tert-butyl)phenol | ≥95% | CAS 2198-66-5 | C10H13BrO | 25g
2-Bromo-4-(tert-butyl)phenol | ≥95% | CAS 2198-66-5 | C10H13BrO | 25g
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