|
| (20S)-3α-Amino-20-hydroxypregn-5-en-18-oic acid γ-lactone Basic information |
| (20S)-3α-Amino-20-hydroxypregn-5-en-18-oic acid γ-lactone Chemical Properties |
| (20S)-3α-Amino-20-hydroxypregn-5-en-18-oic acid γ-lactone Usage And Synthesis |
Description | Gitingensine is a steroidal alkaloid which occurs in Kibatalia gitingensis, being
found mainly in the leaves. It is optically active with a specific rotation of [α]31D
- 65° (CHCI3). The hydrochloride has m.p. 281°C; [α]23D - 59.8° (CHCI3) and
is more readily obtainable in the pure form than the free base. Deamination of
the alkaloid by diazotization gives the deamino derivative, m.p. 235°C. The amino
group may be methylated to yield the N-methyl compound, m.p. 223-4°C but
the base cannot be methylated further. | Definition | ChEBI: Gitingensine is a steroid. It has a role as a metabolite. | References | Anguilar-Santos, Philipp. J. Sci., 94, 217 (1965) |
| (20S)-3α-Amino-20-hydroxypregn-5-en-18-oic acid γ-lactone Preparation Products And Raw materials |
|