terpene

The tree is also the main source of copaene, another terpene.

The reaction can in fact be used to make the terpene, using chlorocamphene.

Some authors will use the term terpene to include all terpenoids.

It produces a large amount of terpene hydrocarbons in its wood and leaves.

Vitamin A is an example of a terpene.

He carried out research on terpene and Indian hemp.

He further demonstrated that in many cases one terpene could be converted into another by applying strong acids or high temperatures.

The Chugaev reaction, which he discovered during his work on thujene an terpene, is named after him.

The name "terpene" is derived from the word "turpentine".

One of the active ingredients of its essential oil is the terpene bisabolol.

Most of the substances are part of the terpene group with limonene being the dominant one.

Sequences containing this protein domain belong to the terpene synthase family.

Like the related acyclic terpene myrcene, ocimenes are unstable in air.

This enzyme is a class I terpene synthase.

Borneol is a bicyclic organic compound and a terpene.

However, plants have an additional terpene pathway in their chloroplasts, a structure fungi do not possess.

The primary known active ingredient of the essential oil from German chamomile is the terpene bisabolol.

Indeed, cannabi- noids are synthesized within the plant from terpene precursors.

Terpene production is also nearing a peak and the floral clusters are beautifully aromatic.

It has been suggested that this gene family be designated tps (for terpene synthase).

The biosynthesis starts with the common terpene farnesyl pyrophosphate.

As a result of low resin production, only a slight terpene aroma and psychoactivity are detectable.

In acidic solutions, geraniol is converted to the cyclic terpene alpha-terpineol.

Limonene is a colourless liquid hydrocarbon classified as a cyclic terpene.

These parts of the plant contain euphorbol (a complex terpene) and other diterpene esters.