| Weight | 117.151 g/mol |
|---|---|
| Formula | C8H7N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
INDOLIZINE (274-40-8)
Score:
#6846 in Chemistry
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- Potent Inhibitors of Secretory Phospholipase A2: Synthesis and Inhibitory Activities of Indolizine and Indene Derivatives (Journal of Medicinal Chemistry, 1996)
- 5-Hydroxytryptamine (5-HT3) receptor antagonists. 1. Indazole and indolizine-3-carboxylic acid derivatives. (Journal of Medicinal Chemistry, 1990)
- Advances in Indolizine Chemistry (Advances in Heterocyclic Chemistry, 1979)
- Plant antitumor agents. 28. Resolution of a key tricyclic synthon, 5'(RS)-1,5-dioxo-5'-ethyl-5'-hydroxy-2'H,5'H,6'H-6'-oxopyrano[3' ,4'- f]delta 6,8-tetrahydro-indolizine: total synthesis and antitumor activity of 20(S)- and 20(R)-camptothecin. (Journal of Medicinal Chemistry, 1987)
- Synthesis of indolizine derivatives with selective antibacterial activity against Mycobacterium tuberculosis (European Journal of Pharmaceutical Sciences, 2007)
- Methods for the Construction of the Indolizine Nucleus (Synthesis, 1976)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=CC=CN2C=C1
-
InChIKeyHOBCFUWDNJPFHB-UHFFFAOYSA-N
- Pubchem - INDOLIZINE
- Wikipedia - indolizine
Indolizine (Chemical formula C8H7N) is a heterocyclic aromatic organic compound that is an isomer of indole. The saturated analog indolizidine forms the structural core of a variety of alkaloids such as swainsonine.
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