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« Previous SpeciesHymeniacidon sanguinea    Next SpeciesHymenia recurvalis »

Semiochemicals of Hymeniacidon sp

Phylum:  Porifera
Subphylum:  
Class:  Demospongiae
Order:  Suberitida
Family:  Halichondriidae
Subfamily:  
Genus:  Hymeniacidon
Tribe:  
Author:  Bowerbank
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Image: Google
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Biology: Google
Distribution: Google



Bedoukain RussellIPM

Semiochemical(s):

  Capon RJ  2002  J. Nat. Prod.  65: 368   
    hymeniacidine    Relative ratio of the component   (*) indicates that compound is active   P
Category of the chemical signal
A -   Attractant
Al -   Allomone
K -   Kairomone
P -   Pheromone
Sy -   Synomone
 
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
Great Australian Bight, Australia 
    me-3-6-bromo-indol-3-yl-E2-propenoate    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
    ethyl-3-6-bromo-indol-3-yl-E2-propenoate    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
    me-3-6-bromo-indol-3-yl-Z2-propenoate    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
    ethyl-3-6-bromo-indol-3-yl-Z2-propenoate    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
 
  Inaba K  1998  J. Nat. Prod.  61: 693   
    spongiacidin A    Relative ratio of the component   (*) indicates that compound is active   P
Category of the chemical signal
A -   Attractant
Al -   Allomone
K -   Kairomone
P -   Pheromone
Sy -   Synomone
 
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
Konbu, Okinawa, Japan 
    spongiacidin B    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
    spongiacidin D    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
    spongiacidin C    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
 
  Kobayashi J  1997b  Tetrahedron  53: 16679   
    tauroacidin A    Relative ratio of the component   (*) indicates that compound is active   P
Category of the chemical signal
A -   Attractant
Al -   Allomone
K -   Kairomone
P -   Pheromone
Sy -   Synomone
 
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
Ishigaki Island, Okinawa, Japan 
    tauroacidin B    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
 
  Kobayashi J  1997a  Tetrahedron  53: 15681   
    konbuacidin A    Relative ratio of the component   (*) indicates that compound is active   P
Category of the chemical signal
A -   Attractant
Al -   Allomone
K -   Kairomone
P -   Pheromone
Sy -   Synomone
 
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
Konbu, Okinawa, Japan 
 
  Tsuda M  1994b  Tetrahedron  50: 4667   
    hymenamide H    Relative ratio of the component   (*) indicates that compound is active   P
Category of the chemical signal
A -   Attractant
Al -   Allomone
K -   Kairomone
P -   Pheromone
Sy -   Synomone
 
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
Manza, Okinawa Island, Japan 
    hymenamide J    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
    hymenamide K    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
    axinastatin 5    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
 
  Kobayashi J  1991c  J. Org. Chem.  56: 4574   
    manzacidin A    Relative ratio of the component   (*) indicates that compound is active   P
Category of the chemical signal
A -   Attractant
Al -   Allomone
K -   Kairomone
P -   Pheromone
Sy -   Synomone
 
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
Manza Beach, Okinawa, Japan 
    manzacidin B    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
    manzacidin C    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
 
  Pettit GR  1990  Can. J. Chem.  68: 1621   
    axinohydantoin    Relative ratio of the component   (*) indicates that compound is active   P
Category of the chemical signal
A -   Attractant
Al -   Allomone
K -   Kairomone
P -   Pheromone
Sy -   Synomone
 
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
Western Caroline Island, Republic of Palau 
    hymenialdisine    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
    debromohymenialdisine    Relative ratio of the component   (*) indicates that compound is active    
Source of the chemical signal
F -   Female
H -   Host (could be of plant or animal origin)
L -   Lure
M -   Male
M&F -   Male and Female
S -   Solider
Q -   Queen
W -   Worker
 
Amount
pg -   Picogram
ng -   Nanogram
g -   Microgram
mg -   Milligram
g -   Gram
 
 
 

Reference(s):

Capon, R.J., Skene, C., Vuong, D., Lacey, E., Gill, J.H., Heiland, K., and Friedel, T. 2002. Equilibrating isomers: bromoindoles and a seco-xanthine encountered during a study of nematocides from the Southern Australian marine sponge Hymeniacidon sp. J. Nat. Prod. 65:368-370.
 
Inaba, K., Sato, H., Tsuda, M., and Kobayashi, J. 1998. Spongiacidins A-D, new bromopyrrole alkaloids from Hymeniacidon sponge. J. Nat. Prod. 61:693-695.
 
Kobayashi, J., Inaba, K., and Tsuda, M. 1997b. Tauroacidins A and B, new bromopyrrole alkaloids possessing a taurine residue from Hymeniacidon sponge. Tetrahedron. 46:16679-16682.
 
Kobayashi, J., Suzuki, M., and Tsuda, M. 1997a. Konbu'acidin A, a new bromopyrrole alkaloid with cdk4 inhibitory activity from Hymeniacidon sponge. Tetrahedron. 53:15681-15684.
 
Tsuda, M., Sasaki, T., and Kobayashi, J. 1994b. Hymenamides G, H, J, and K, four new cyclic octapeptides from the Okinawan marine sponge Hymeniacidon sp. Tetrahedron. 50:4667-4680.
 
Kobayashi, J., Kanda, F., Ishibashi, M., and Shigemori, H. 1991c. Manzacidins A-C, novel tetrahydropyrimidine alkaloids from the Okinawan marine sponge Hymeniacidon sp. J. Org. Chem. 56:4574-4576.
 
Pettit, G.R., Herald, C.L., Leet, J.E., Gupta, R., Schaufelberger, D.E., Bates, R.B., Clewlow, P.J., Doubek, D.L., Manfredi, K.P., Rtzler, K., Schmidt, J.M., Tackett, L.P., Ward, F.B., Bruck, M., and Camou, F. 1990. Antineoplastic agents. 168. Isolation and structure of axinohydantoin. Can. J. Chem. 68:1621-1624.
 
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
Ⓒ 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 9-June-2024