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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Grade
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Physical Form
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Percent Purity
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- (3)
- (4)
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1
Ethyl acrylate, 99%, stab. with ca 20ppm 4-methoxyphenol
CAS: 140-88-5 Molecular Formula: C5H8O2 Molecular Weight (g/mol): 100.12 MDL Number: MFCD00009188 InChI Key: JIGUQPWFLRLWPJ-UHFFFAOYSA-N Synonym: ethyl acrylate,acrylic acid ethyl ester,ethyl propenoate,2-propenoic acid, ethyl ester,ethyl 2-propenoate,ethylacrylaat,ethylakrylat,etil acrilato,acrylic acid, ethyl ester,aethylacrylat PubChem CID: 8821 ChEBI: CHEBI:82327 IUPAC Name: ethyl prop-2-enoate SMILES: CCOC(=O)C=C
| PubChem CID | 8821 |
|---|---|
| CAS | 140-88-5 |
| Molecular Weight (g/mol) | 100.12 |
| ChEBI | CHEBI:82327 |
| MDL Number | MFCD00009188 |
| SMILES | CCOC(=O)C=C |
| Synonym | ethyl acrylate,acrylic acid ethyl ester,ethyl propenoate,2-propenoic acid, ethyl ester,ethyl 2-propenoate,ethylacrylaat,ethylakrylat,etil acrilato,acrylic acid, ethyl ester,aethylacrylat |
| IUPAC Name | ethyl prop-2-enoate |
| InChI Key | JIGUQPWFLRLWPJ-UHFFFAOYSA-N |
| Molecular Formula | C5H8O2 |
2
Transcrocetin, MedChemExpress
MedChemExpress Transcrocetin (trans-Crocetin), extracted from saffron (Crocus sativus L.), acts as an NMDA receptor antagonist with high affinity. Transcrocetin (trans-Crocetin) is capable of crossing the blood-brain barrier and reach the central nervous system (CNS).
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| Molecular Weight (g/mol) | 328.4 |
|---|---|
| Color | Orange |
| Physical Form | Solid |
| Chemical Name or Material | Transcrocetin |
| Grade | Research |
| SMILES | O=C(O)/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C(O)=O |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 98.0% |
| CAS | 27876-94-4 |
| Solubility Information | DMSO : 1 mg/mL (3.05 mM; Need ultrasonic and warming) |
| Synonym | trans-Crocetin |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣The compound is unstable in solutions, freshly prepared is recommended. |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣The compound is unstable in solutions, freshly prepared is recommended. |
| Molecular Formula | C20H24O4 |
| Formula Weight | 328.4 |
3
Caftaric acid, MedChemExpress
MedChemExpress Caftaric acid is a natural product.
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| Molecular Weight (g/mol) | 312.23 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Caftaric acid |
| Grade | Research |
| SMILES | O=C(O)[C@H](OC(/C=C/C1=CC=C(O)C(O)=C1)=O)[C@@H](O)C(O)=O |
| Percent Purity | 99.04% |
| CAS | 67879-58-7 |
| Solubility Information | H2O : 50 mg/mL (160.14 mM; Need ultrasonic) ∣DMSO : 50 mg/mL (160.14 mM; Need ultrasonic) |
| Synonym | trans-Caftaric acid |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C13H12O9 |
| Formula Weight | 312.23 |
4
Cynaropicrin, MedChemExpress
MedChemExpress Cynaropicrin is a sesquiterpene lactone which can inhibit tumor necrosis factor (TNF-α) release with IC50s of 8.24 and 3.18 μM for murine and human macrophage cells, respectively. Cynaropicrin also inhibits the increase of cartilage degradation factor (MMP13) and suppresses NF-κB signaling.
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| Molecular Weight (g/mol) | 346.37 |
|---|---|
| Color | Colorless |
| Physical Form | Oil |
| Chemical Name or Material | Cynaropicrin |
| Grade | Research |
| SMILES | C=C([C@H]1O)[C@]([C@@]2([H])C1)([H])[C@](OC3=O)([H])[C@@](C3=C)([H])[C@@H](OC(C(CO)=C)=O)CC2=C |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 97.16% |
| CAS | 35730-78-0 |
| Solubility Information | DMSO : ≥ 50 mg/mL (144.35 mM) |
| Health Hazard 1 | H317 |
| Purity Grade Notes | Research |
| Recommended Storage | -20°C, protect from light∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light) |
| Shelf Life | -20°C, protect from light∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light) |
| Molecular Formula | C19H22O6 |
| Formula Weight | 346.37 |
5
Sortin1, MedChemExpress
MedChemExpress Sortin1 is a chemical genetic-hit molecule that causes specific mislocalization of plant and yeast-soluble and membrane vacuolar markers.
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| Molecular Weight (g/mol) | 441.43 |
|---|---|
| Color | Red |
| Physical Form | Solid |
| Chemical Name or Material | Sortin1 |
| Grade | Research |
| SMILES | O=C(C1=C(C)NC2=C(C(C3=C2C=CC=C3)=O)C1C4=CC=C(C5=CC=C(C(O)=O)C=C5)O4)OC |
| Percent Purity | 98.29% |
| CAS | 503837-98-7 |
| Solubility Information | DMSO : 100 mg/mL (226.54 mM; Need ultrasonic) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C26H19NO6 |
| Formula Weight | 441.43 |
6
Micheliolide, MedChemExpress
MedChemExpress Micheliolide could effectively attenuate the high glucose-stimulated activation of NF-κB, the degradation of IκBα, and the expression of MCP-1, TGF-β1 and FN in rat mesangial cells (MCs).
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| Molecular Weight (g/mol) | 248.32 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Micheliolide |
| Grade | Research |
| SMILES | O=C(O[C@@]1([H])[C@@]2([H])CCC(C)=C3CC[C@@](C)(O)[C@@]31[H])C2=C |
| Percent Purity | 99.17% |
| CAS | 68370-47-8 |
| Solubility Information | DMSO : 100 mg/mL (402.71 mM; Need ultrasonic) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C15H20O3 |
| Formula Weight | 248.32 |
7
CID-797718, MedChemExpress
MedChemExpress CID-797718 is a compound with unknown details.
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| Molecular Weight (g/mol) | 217.22 |
|---|---|
| Color | Brown |
| Physical Form | Solid |
| Chemical Name or Material | CID-797718 |
| Grade | Research |
| SMILES | O=C1OC2=CC=C(O)C=C2C3=C1NCCC3 |
| Percent Purity | 99.09% |
| CAS | 370586-05-3 |
| Solubility Information | DMSO : ≥ 49 mg/mL (225.58 mM) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C12H11NO3 |
| Formula Weight | 217.22 |
8
Acenocoumarol, MedChemExpress
MedChemExpress Acenocoumarol is an anticoagulant that functions as a Vitamin K antagonist.
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| Molecular Weight (g/mol) | 353.33 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Acenocoumarol |
| Grade | Research |
| SMILES | O=C1C(C(C2=CC=C([N+]([O-])=O)C=C2)CC(C)=O)=C(O)C3=CC=CC=C3O1 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.0% |
| CAS | 152-72-7 |
| Solubility Information | DMSO : 100 mg/mL (283.02 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C19H15NO6 |
| Formula Weight | 353.33 |
9
RG7834, MedChemExpress
MedChemExpress RG7834 (RO 7020322) is a highly selective and orally bioavailable HBV inhibitor, potently inhibits HBV antigens (both HBsAg and HBeAg) and HBV DNA, with IC50s of 2.8, 2.6, and 3.2 nM, respectively, in dHepaRG Cells.
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10
Dihydromethysticin, MedChemExpress
MedChemExpress Dihydromethysticin is one of the six major kavalactones found in the kava plant; has marked activity on the induction of CYP3A23.
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| Molecular Weight (g/mol) | 276.28 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Dihydromethysticin |
| Grade | Research |
| SMILES | O=C1C=C(OC)C[C@H](CCC2=CC=C(OCO3)C3=C2)O1 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.0% |
| CAS | 19902-91-1 |
| Solubility Information | DMSO : 100 mg/mL (361.95 mM; Need ultrasonic) |
| Synonym | (+)-Dihydromethysticin |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, protect from light∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light) |
| Shelf Life | 4°C, protect from light∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light) |
| Molecular Formula | C15H16O5 |
| Formula Weight | 276.28 |
11
Isocorynoxeine, MedChemExpress
MedChemExpress Isocorynoxeine, an isorhynchophylline-related alkaloid, exhibits a dose-dependent inhibition of 5-HT2A receptor-mediated current response with an IC50 of 72.4 μM.
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| Molecular Weight (g/mol) | 382.45 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Isocorynoxeine |
| Grade | Research |
| SMILES | O=C(NC1=C2C=CC=C1)[C@@]32[C@@](C[C@H](/C(C(OC)=O)=C\OC)[C@@H](C=C)C4)([H])N4CC3 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 99.95% |
| CAS | 51014-29-0 |
| Solubility Information | DMSO : 25 mg/mL (65.37 mM; Need ultrasonic) |
| Synonym | 7-Isocorynoxeine |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C22H26N2O4 |
| Formula Weight | 382.45 |
12
Imperatorin, MedChemExpress
MedChemExpress Imperatorin is an effective of NO synthesis inhibitor (IC50=9.2 μmol), which also is a BChE inhibitor (IC50=31.4 μmol). Imperatorin is a weak agonist of TRPV1 with EC50 of 12.6±3.2 μM.
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| Molecular Weight (g/mol) | 270.28 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Imperatorin |
| Grade | Research |
| SMILES | O=C1C=CC2=CC3=C(OC=C3)C(OC/C=C(C)/C)=C2O1 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 98.0% |
| CAS | 482-44-0 |
| Solubility Information | DMSO : 50 mg/mL (184.99 mM; Need ultrasonic) |
| Health Hazard 1 | H315∣H319∣H335 |
| Synonym | Ammidin |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C16H14O4 |
| Formula Weight | 270.28 |
13
Phenprocoumon, MedChemExpress
MedChemExpress Phenprocoumon is a coumarin derivative that acts as a long acting oral anticoagulant and an antagonist of vitamin K.
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| Molecular Weight (g/mol) | 280.32 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Phenprocoumon |
| Grade | Research |
| SMILES | O=C1C(C(C2=CC=CC=C2)CC)=C(O)C3=CC=CC=C3O1 |
| Percent Purity | 98.09% |
| CAS | 435-97-2 |
| Solubility Information | DMSO : ≥ 125 mg/mL (445.92 mM) |
| Health Hazard 1 | H301+H311+H331∣H361∣H373 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C18H16O3 |
| Formula Weight | 280.32 |
14
MDL 105519, MedChemExpress
MedChemExpress MDL 105519 is a potent and selective antagonist of glycine binding to the NMDA receptor.
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| Molecular Weight (g/mol) | 376.19 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | MDL 105519 |
| Grade | Research |
| SMILES | O=C(O)C(N1)=C(/C=C(C2=CC=CC=C2)/C(O)=O)C3=C1C=C(Cl)C=C3Cl |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 97.15% |
| CAS | 161230-88-2 |
| Solubility Information | DMSO : 17 mg/mL (45.19 mM; Need ultrasonic and warming) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C18H11Cl2NO4 |
| Formula Weight | 376.19 |
15
Isradipine, MedChemExpress
MedChemExpress Isradipine (PN 200-110) is an orally active L-type calcium channel blocker. Isradipine, as a powerful peripheral vasodilator, is a dihydropyridine calcium antagonist with selective actions on the heart as well as the peripheral circulation. Isradipine is a potentially viable neuroprotective agent for Parkinson's disease.
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| Molecular Weight (g/mol) | 371.39 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Isradipine |
| Grade | Research |
| SMILES | O=C(C1=C(C)NC(C)=C(C(OC(C)C)=O)C1C2=CC=CC3=NON=C23)OC |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.69% |
| CAS | 75695-93-1 |
| Solubility Information | DMSO : ≥ 100 mg/mL (269.26 mM) |
| Synonym | PN 200-110 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C19H21N3O5 |
| Formula Weight | 371.39 |