Artificial intelligent assistant

stilbene

answer Answers

ProphetesAI is thinking...

MindMap

Sources

1
stilbene
stilbene Chem. (ˈstɪlbiːn) [f. Gr. στίλβειν to glitter + -ene.] A hydrocarbon produced by the action of heated lead oxide on toluene, and in various other ways: used in dye-stuffs. So ˈstilbin [see -in] in the same sense.1868 Watts Dict. Chem. V. 431 Stilbene. Ibid. 432 Stilbin. Syn. with Stilbene. ... Oxford English Dictionary
prophetes.ai 0.0 3.0 0.0
2
Stilbene
Stilbene may refer to one of the two stereoisomers of 1,2-diphenylethene: (E)-Stilbene (trans isomer) (Z)-Stilbene (cis isomer) See also Stilbenoids wikipedia.org
en.wikipedia.org 0.0 1.5 0.0
3
(E)-Stilbene
Isomers Stilbene exists as two possible stereoisomers. One is trans-1,2-diphenylethylene, called (E)-stilbene or trans-stilbene. For example, using tert-butyl hydroperoxide, oxidation of cis-stilbene produces 0.8% cis-stilbene oxide, 13.5% trans-stilbene oxide, and 6.1% benzaldehyde wikipedia.org
en.wikipedia.org 0.0 0.90000004 0.0
4
stilbamidine
stilbamidine Pharm. (stɪlˈbæmɪdiːn) [f. stilbene + amidine (f. amide + -ine5).] A diamidine derivative, (H2N)(HN)C·C6H4·CH:CH·C6H4·C(NH)(NH2), of stilbene which has antiprotozoal properties and has been used, usu. in the form of its isethionate, in the treatment of trypanosomiasis and leishmaniasis.... Oxford English Dictionary
prophetes.ai 0.0 0.6 0.0
5
(Z)-Stilbene
Isomers Stilbene exists as two possible isomers known as (E)-stilbene and (Z)-stilbene. Stilbene can undergo stilbene photocyclization, an intramolecular reaction. (Z)-Stilbene can undergo electrocyclic reactions. wikipedia.org
en.wikipedia.org 0.0 0.6 0.0
6
Stilbene synthase
Stilbene synthase may refer to: Pinosylvin synthase (Pine stilbene synthase) Trihydroxystilbene synthase (Resveratrol synthase) wikipedia.org
en.wikipedia.org 0.0 0.3 0.0
7
Meso-Stilbene dibromide
meso-Stilbene dibromide is an organic compound with a formula of (C6H5CH(Br))2.It is one of three isomeric stilbene dibromides, the others being the pair Synthesis and reactions meso-Stilbene dibromide can be prepared by treatment of (E)-stilbene with bromine. wikipedia.org
en.wikipedia.org 0.0 0.3 0.0
8
Stilbenoid
Stilbenoids are hydroxylated derivatives of stilbene. They have a C6–C2–C6 structure. Under UV irradiation, stilbene and its derivatives undergo intramolecular cyclization, called stilbene photocyclization to form dihydrophenanthrenes. wikipedia.org
en.wikipedia.org 0.0 0.3 0.0
9
Diphenylethylene
Diphenylethylene or Diphenylethene may refer to: 1,1-Diphenylethylene 1,2-Diphenylethylene, or Stilbene (E)-Stilbene (trans-isomer) (Z)-Stilbene ( wikipedia.org
en.wikipedia.org 0.0 0.3 0.0
10
Diarylethene
The simplest example is stilbene, which has two geometric isomers, E and Z. The activation energy for thermal E-Z isomerization is 150–190 kJ mol−1 for stilbene, meaning that temperatures above 200°C are required to isomerize stilbene wikipedia.org
en.wikipedia.org 0.0 0.3 0.0
11
Mallory reaction
Under UV irradiation, stilbene and its derivatives undergo intramolecular cyclization to form dihydrophenanthrenes. Aryl enynes, heteroatomic stilbene derivatives (e.g. amides), and substrates containing a single heteroatom in place of the stilbene double bond also undergo wikipedia.org
en.wikipedia.org 0.0 0.0 0.0
12
Trihydroxystilbene synthase
enzymology, a trihydroxystilbene synthase () is an enzyme that catalyzes the chemical reaction 3 malonyl-CoA + 4-coumaroyl-CoA 4 CoA + 3,4',5-trihydroxy-stilbene Other names in common use include resveratrol synthase, and stilbene synthase. This enzyme participates in phenylpropanoid biosynthesis. wikipedia.org
en.wikipedia.org 0.0 0.0 0.0
13
Ampelopsin (compound)
Ampelopsin may refer to: Ampelopsin, a flavanonol Ampelopsin A, a stilbene oligomer Ampelopsin B, a stilbene oligomer Ampelopsin C, a stilbene oligomer Ampelopsin D, a stilbene oligomer Ampelopsin E, a stilbene oligomer Ampelopsin F, a stilbene oligomer References wikipedia.org
en.wikipedia.org 0.0 0.0 0.0
14
Parthenocissus laetevirens
Parthenocissus laetevirens contains the stilbene oligomers laetevirenol A, B, C, D and E, the stilbene tetramers laetevirenol F and G as well as the dimers wikipedia.org
en.wikipedia.org 0.0 0.0 0.0
15
Pinosylvin synthase
Other names in common use include stilbene synthase, and pine stilbene synthase. This enzyme participates in phenylpropanoid biosynthesis. wikipedia.org
en.wikipedia.org 0.0 0.0 0.0