Acrylic acids and derivatives

Organic compounds that consist of a carboxylic acid with a vinyl functional group substitution; vinyl functional groups are a carbon - carbon double bond. Includes compounds that are derived from acrylic acids.

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1,051 – 1,065 of 2,636 results

1,051

Aobchem AOBCHEM

5001048359 6-BROMO-3-CHLOROPYRIDIN-2 1H -

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1,052

Aobchem AOBCHEM

5001048604 6-BROMO-3-CHLOROPYRIDIN-2 1H -

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1,053

Aobchem AOBCHEM

5001053612 2- 3 5-DIMETHYLPHENOXY ACETONI

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1,054

Aobchem AOBCHEM

5001054413 5-BROMO-6-CHLOROPYRIDIN-2-AMIN

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1,055

Aobchem AOBCHEM

5001054414 5-BROMO-6-CHLOROPYRIDIN-2-AMIN

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1,056

eMolecules 1211530-21-0 | 2-(4-Bromopyridin-2-yl)acetic acid | Ambeed | MFCD09999987 | 216.034 | C7H6BrNO2 | 97.000 | OC(=O)Cc1cc(Br)ccn1 | 100mg | 525115931

2-(4-Bromopyridin-2-yl)acetic acid | Ambeed | 1211530-21-0 | MFCD09999987 | 216.034 | C7H6BrNO2 | 97.000 | OC(=O)Cc1cc(Br)ccn1 | 100mg | 525115931

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1,057

eMolecules 81485-25-8 | Medchem Express | Peretinoin | 5mg | 446254726 | HY-100008 | MFCD01742209 | 302.458 | C20H30O2

Medchem Express | Peretinoin | 5mg | 446254726 | HY-100008 | 81485-25-8 | MFCD01742209 | 302.458 | C20H30O2

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1,058

Medchemexpress LLC TBOPP | 1996629-79-8 | 99.6% | 490.49 | C24H21F3N2O4S | 50MG

TBOPP is a small-molecule research reagent that selectively inhibits DOCK1. It blocks DOCK1-mediated Rac activation with an IC50 of 8.4 μM and binds the DOCK1 DHR-2 domain with a Kd of 7.1 μM. TBOPP has shown anti-tumor activity in preclinical studies and is provided as a high-purity compound with available powder and DMSO solution formats for biochemical and cellular experiments.

High purity suitable for research applications.
Selective inhibitor of DOCK1 with IC50 8.4 μM and Kd 7.1 μM.
Demonstrated anti-tumor activity in preclinical models.
Available as powder and as a DMSO solution for flexible dosing.
Comes with supporting documentation such as datasheet, COA, and SDS.
Stable under recommended cold storage for long-term preservation.

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1,059

Cayman Chemical OlenolIc AcId Acrylate 10mg

An agonist of 5-HT1A and a derivative of oleanolic acid; acts as an agonist at the 5-HT1A receptor in mouse hippocampal homogenates in a [35S]GTPγS binding assay (EC50 = 0.79 µM); a selective inhibitor of MAO-A over MAO-B (IC50s = 48.8 µM and >100 µM, respectively); reduces immobility in the forced swim test and increases the number of crossings and time spent at the center in the open field test, indicating anti-depressant-like and anxiolytic activities in mice at 10 mg/kg