| Weight | 634.213 g/mol |
|---|---|
| Formula | C37H44ClNO6 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
penitrem A (12627-35-9)
penitrem D · penitrem E · penitrem B
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- Tremorgenic Indole Alkaloids. The Total Synthesis of ()-Penitrem D (Journal of the American Chemical Society, 2003)
- Total Synthesis of ()-Penitrem D (Journal of the American Chemical Society, 2000)
- Tremorgenic indole alkaloid studies. 6. Preparation of an advanced intermediate for the synthesis of penitrem D. Synthesis of an indole oxocane (Tetrahedron, 1989)
- Tremorgenic Indole Alkaloids. 9. Asymmetric construction of an Advanced F-G-H-ring Lactone precursor for the Synthesis of Penitrem D (Journal of Organic Chemistry, 1995)
- Radical and palladium-catalyzed cyclizations to cyclobutenes: An entry to the BCD ring system of penitrem D (Journal of Organic Chemistry, 2004)
- An end-game strategy for construction of the G-H-I rings of penitrem D, a tremorgenic indole alkaloid (Tetrahedron Letters, 1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - penitrem D
- penitrem E
- penitrem B
- tremortin
- penitrems
- tremortin B
- tremortin A
-
SMILESCC(=C)C1C(C2C3(O2)C(O1)CCC4(C3(CCC5C4(C6=C7C5OC(C8CC9C8(C1=C7C(=CC(=C1CC9=C)Cl)N6)O)(C)C)C)O)C)O
-
InChIKeyJDUWHZOLEDOQSR-UHFFFAOYSA-N
- Pubchem - penitrem A
- Wikipedia - Penitrem A
Penitrem A (tremortin) is a fungal neurotoxin found on ryegrass. It is produced by certain species of Aspergillus, Claviceps, and Penicillium. It inhibits potassium channels in smooth muscles.
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penitrem A
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