475-67-2
475-67-2
Chemical Structure
Isocorydine
- CAS No.: 475-67-2
- Formula:C20H23NO4
- Molecular Weight:341.40
IUPAC Name: (S)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-11-ol
InChIKey: QELDJEKNFOQJOY-ZDUSSCGKSA-N
SMILES: COC1=C2C3=C(C=C1OC)CCN(C)[C@@]3([H])CC4=CC=C(OC)C(O)=C24
Biological Activity: Isocorydine is isolated from Dicranostigma leptopodum (Maxim.) Fedde (DLF). Isocorydine combines with Doxorubicin (DOX) has a promising potential to eradicate hepatocellular carcinoma (HCC)[1].
| Cat. No. | 상품명 | Purity | 제품 설명 | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Isocorydine | 99.95% | Isocorydine is isolated from Dicranostigma leptopodum (Maxim.) Fedde (DLF). Isocorydine combines with Doxorubicin (DOX) has a promising potential to eradicate hepatocellular carcinoma (HCC). | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Isocorydine (Standard) | ≥98% | Isocorydine is isolated from Dicranostigma leptopodum (Maxim.) Fedde (DLF). Isocorydine combines with Doxorubicin (DOX) has a promising potential to eradicate hepatocellular carcinoma (HCC). | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2,3,5,6-Tetramethoxyaporphine | 2,3,5,6-Tetramethoxyaporphine is an antitussive agent, a medicinally valuable benzyl isoquinoline alkaloid. 2,3,5,6-Tetramethoxyaporphine can be isolated from the yellow hornpoppy, Glaucium flavum Cr. (Fam. Papaveraceae). | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Isocorytuberine | Isocorytuberine is an alkaloid. Isocorytuberine can be isolated and purified from the whole plant of Dicranostigma leptopodum (Maxim.) Fedde (DLF). | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Norisocorydine | Norisocorydine ((+)-Norisocorydine) is an aporphine alkaloid with antinociceptive and radical scavenging effects. Norisocorydine shows a SC50 of 14.1 μg/mL in DPPH radical scavenging test. Norisocorydine exhibits antinociceptive ability in mice. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Corytuberine | Corytuberine is an aporphine alkaloid found in Dicranostigma leptopodum. Corytuberine displays cytotoxicity against SMMC-7721 tumor cells. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Corydine | 99.93% | Corydine is a HIV-1 reverse transcriptase inhibitor and μ-opioid receptor (MOR) agonist, with an IC50 of 356.7 μg/mL against HIV-1 reverse transcriptase, an EC50 of 0.51 μM for MOR, and a Ki of 2.82 μM for MOR. Corydine produces antinociceptive effects by inhibiting acetic acid-induced writhing behavior in a MOR-dependent manner. Corydine inhibits the proliferation of cancer cells, mitogen-stimulated lymphocytes and IL-2-dependent cells. Corydine can be used in studies related to human immunodeficiency virus infection, visceral pain, leukemia, melanoma, bladder cancer and colon adenocarcinoma. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Isocorydine hydrochloride | Isocorydine hydrochloride is isolated from Dicranostigma leptopodum (Maxim.) Fedde (DLF). Isocorydine hydrochloride combines with Doxorubicin (DOX) has a promising potential to eradicate hepatocellular carcinoma (HCC). | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
N-Methyllindcarpine | N-Methyllindcarpine is a Alkaloids product that can be isolated from the barks of Lindera pipericarpa. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Litseglutine B | Litseglutine B is a Alkaloids product that can be isolated from the herbs of Litsea glutinosa. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Lauroscholtzine | 99.81% | Lauroscholtzine (N-Methyllaurotetanine), a natural alkaloid, is a 5-HT1A receptor agonist. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Glaucine (Standard) | ≥98% | Glaucine (Standard) is the analytical standard of Glaucine. This product is intended for research and analytical applications. Glaucine (O,O-Dimethylisoboldine) is an alkaloid isolated from Glaucium flavum with antitussive, bronchodilation and anti-inflammatory properties. Glaucine is a selective and orally active phosphodiesterase 4 (PDE4) inhibitor with Kis of 3.4 μM in human bronchus and polymorphonuclear leukocytes. Glaucine is also a non-selective α-adrenoceptor antagonist, a Ca2+ entry blocker, and a weak dopamine D1 and D2 receptor antagonist. Glaucine has antioxidative and antiviral activities. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
