Unsubstituted Phenols
eMolecules 5306-98-9 | 5-chloro-2-methyl-phenol | Synthonix | MFCD00060672 | 142.580 | C7H7ClO | 95.000 | Cc1ccc(Cl)cc1O | 25g | 808569714
5-chloro-2-methyl-phenol | Synthonix | 5306-98-9 | MFCD00060672 | 142.580 | C7H7ClO | 95.000 | Cc1ccc(Cl)cc1O | 25g | 808569714
Sigma Aldrich Fine Chemicals Biosciences L-(-)-Norepinephrine (+)-bitartrate salt monohydrate meets USP testing specifications | 108341-18-0 | MFCD00150449 | 5G
L-(-)-Norepinephrine (+)-bitartrate salt monohydrate meets USP testing specifications | Mol Wt: 337.28 | 108341-18-0 | MFCD00150449 | 5G
eMolecules 33576-77-1 | 4-Methylamino-phenol hydrobromide | J & W PharmLab, LLC | MFCD12913690 | 204.067 | C7H10BrNO | 96.000 | Br.CNc1ccc(O)cc1 | 5g | 249975798
4-Methylamino-phenol hydrobromide | J & W PharmLab, LLC | 33576-77-1 | MFCD12913690 | 204.067 | C7H10BrNO | 96.000 | Br.CNc1ccc(O)cc1 | 5g | 249975798
Medchemexpress LLC SN-011 | 2249435-90-1 | C25H19FN2O4S | 10MG
This small-molecule STING inhibitor blocks STING activation by competing with cyclic dinucleotides for the STING binding pocket, reducing downstream interferon signaling. It is reported to inhibit mouse and human STING with an IC50 of 76 nM and is intended for research into STING-driven immune signaling, inflammation, and autoimmunity.
- Potent STING antagonist with reported IC50 of 76 nM.
- Active against mouse and human STING.
- Competitive inhibitor of cyclic dinucleotide binding.
- Provided with analytical data including COA, H NMR, RP-HPLC, and MS.
- Suitable for cell-based and biochemical studies of innate immune signaling.
![eMolecules 31677-74-4 | 2-(6-Benzyloxyindolyl)ethylamine Hemisulfate | Toronto Research Chemicals630.760 | C34H38N4O6SOS(O)(=O)=O.NCCc1c[nH]c2cc(OCc3ccccc3)ccc12.NCCc1c[nH]c2cc(OCc3ccccc3)ccc12 | 100mg | 483383598](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502177644.JPG-250.jpg)
eMolecules 31677-74-4 | 2-(6-Benzyloxyindolyl)ethylamine Hemisulfate | Toronto Research Chemicals630.760 | C34H38N4O6SOS(O)(=O)=O.NCCc1c[nH]c2cc(OCc3ccccc3)ccc12.NCCc1c[nH]c2cc(OCc3ccccc3)ccc12 | 100mg | 483383598
2-(6-Benzyloxyindolyl)ethylamine Hemisulfate | Toronto Research Chemicals | 31677-74-4630.760 | C34H38N4O6SOS(O)(=O)=O.NCCc1c[nH]c2cc(OCc3ccccc3)ccc12.NCCc1c[nH]c2cc(OCc3ccccc3)ccc12 | 100mg | 483383598
Medchemexpress LLC Procyanidin B3 | 23567-23-9 | 1 MG
Procyanidin B3 is a natural product known for its antioxidant activity, oral bioavailability, and ability to penetrate the blood-brain barrier. It acts as a selective inhibitor of histone acetyltransferase (HAT), specifically by inhibiting p300 HAT-mediated acetylation of the androgen receptor. This product also helps alleviate intervertebral disc degeneration (IVDD) by inhibiting the formation of the TLR4/MD-2 complex.
- Exhibits antioxidant activity
- Possesses oral bioavailability and blood-brain barrier penetration
- Functions as a selective histone acetyltransferase (HAT) inhibitor
- Specifically inhibits p300 HAT-mediated acetylation of the androgen receptor
- Alleviates intervertebral disc degeneration (IVDD) by inhibiting TLR4/MD-2 complex formation
- Applicable for research in prostate cancer and arthritis
- Does not affect HDAC or HMT (histone methyltransferase)
Medchemexpress LLC Cardamonin | 18956-16-6 | MFCD00238554 | 98.4% | 270.28 g/mol | C16H14O4 | 10 MG
Cardamonin is a chalcone-class flavonoid research compound supplied for laboratory use. It is provided as a 10 mg pack (C16H14O4, 270.28 g/mol) and is commonly used in cell-based and biochemical studies involving inflammatory and cancer signaling pathways. For research use only.
- Purity of 98.4%.
- Chemical formula C16H14O4 and molecular weight 270.28 g/mol.
- Suitable for cell-based and biochemical assays.
- Provided as a 10 mg pack for laboratory use.
- Synonyms include cardamomin and alpinetin chalcone.
Medchemexpress LLC HY-15237 1mg Medchemexpress, SL 0101-1 CAS:77307-50-7 Purity:>98%
Medchemexpress, HY-15237 1mg SL 0101-1 CAS:77307-50-7 SL 0101-1 (SL0101), a kaempferol glycoside, isolated from the tropical plant F. refracta, is a cell-permeable, selective, reversible, ATP-competitive p90 Ribosomal S6 Kinase (RSK) inhibitor, with an IC 50 of 89 nM. Shows proliferation inhibition in human breast cancer cell line MCF-7 and produces a cell cycle block in G 1 phase [1] . 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.
Medchemexpress LLC HY-103638A 100mg Medchemexpress, 3-Methoxytyramine CAS:554-52-9 Purity:>98%
Medchemexpress, HY-103638A 100mg 3-Methoxytyramine CAS:554-52-9 3-Methoxytyramine, a well known extracellular metabolite of 3-hydroxytyramine/dopamine, is a neuromodulator. 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.
Selleck Chemical LLC Bephenium Hydroxynaphthoate S4389-50mg
Bephenium(NSC 759245) is an activator of B-type Acetylcholine receptor (AChR) Bephenium selectively activates the Hco-L-AChR1 subtype made of Hco-UNC-29 1 Hco-UNC-38 Hco-UNC-63 Hco-ACR-8 subunits Bephenium hydroxynaphthoate is an anthelmintic agent formerly used in the treatment of hookworm infections and ascariasis
Medchemexpress LLC HY-110263 5mg Medchemexpress, EML 425 CAS:1675821-32-5 Purity:>98%
Medchemexpress, HY-110263 5mg EML 425 CAS:1675821-32-5 EML425 is a potent and selective CREB binding protein (CBP)/p300 inhibitor with IC50s of 2.9 and 1.1 μM, respectively. 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.