Details of Natural Product (NP)

General Information of Natural Product (ID: NP1598)
  Natural Product Name
Ammonia
  Synonyms
ammonia; 7664-41-7; azane; Ammonia gas; Spirit of hartshorn; Nitro-sil; Ammonia, anhydrous; Ammoniakgas; Ammonia solution; Ammonia anhydrous; Anhydrous ammonia; Ammoniak; AM-Fol; Liquid Ammonia; Ammoniak Kconzentrierter; Amoniak [Polish]; Ammoniac [French]; Ammoniak [German]; ammoniac; Ammoniaca [Italian]; Caswell No. 041; Ammonia (conc 20% or greater); CCRIS 2278; HSDB 162; Ammonia solution, strong; NH3; UN 2073 (>44% solution); UN1005; Aminomethyl Polystyrene Resin; Refrigerent R717; EPA Pesticide Chemical Code 005302; UNII-5138Q19F1X; Strong Ammonia Solution; R 717; UN 1005 (anhydrous gas or >50% solution); UN 2672 (between 12% and 44% solution); Ammonia, 7M in methanol; Ammonia anhydrous, 99.98%; CHEBI:16134; MFCD00011418; 5138Q19F1X; Ammonia solution, strong (NF); Ammonia solution, strong [NF]; amoniaco; Ammoniaca; Amoniak; (Aminomethyl)polystyrene; EINECS 231-635-3; tertiaeres Amin; Aminyl radical; ammonia ca; primaeres Amin; Ammonia inhalant; Ammonia,aromatic; Ammonia-solution; Ammoniacum gummi; sekundaeres Amin; anyhydrous ammonia; Ammonium causticum; (Aminomethyl)polystyrene, 100-200 mesh, extent of labeling: ~0.5 mmol/g amine loading; NH4; UNX; Strong-ammonia solution; R 717 (ammonia); Ammonia (8CI,9CI); Ammonia water (JP15); Aromatic ammonia vaporole; Ammonia, 2M in methanol; Dowex(R) 66 free base; Ammonia, 0.5M in THF; Aromatic Ammonia, Vaporole; EC 231-635-3; Ammonia solution strong (NF); Ammonia solution strong [usan]; INS NO.527; N H3; ammonium isovalerate 30% in pg; CHEMBL1160819; DTXSID0023872; DTXSID40912315; DTXSID80420101; INS-527; [NH3]; NH(3); 2-Methylamino-5-nitro-benzonitrile; Ammonia solution, 0.4 M in THF; Ammonia solution, 4 M in methanol; Ammonia solution, 7 N in methanol; Ammonia, anhydrous, >=99.98%; ACT02989; Ammonia solution 2.0 M in ethanol; Ammonia solution 2.0 M in methanol; Ammonia solution, 0.5 M in dioxane; Ammonia solution, 2.0 M in ethanol; AKOS015916403; Ammonia anhydrous 170g Lecture bottle; Ammonia solution, 2.0 M in methanol; Ammonia solution 2.0 M in isopropanol; MCULE-5646000632; Ammonia 0.5M solution in 1,4-Dioxane; Ammonia solution, 2.0 M in isopropanol; Ammonia (includes anhydrous ammonia and aqueous ammonia from water dissociable ammonium salts and other sources; 10% of total aqueous ammonia is reportable under this listing); Ammonia, anhydrous, liquefied or ammonia solutions, relative density <0.880 at 15 C in water, with >50% ammonia [UN1005] [Nonflammable gas]; Ammonia, anhydrous, liquefied or ammonia solutions, relative density <0.880 at 15 C in water, with >50% ammonia [UN1005] [Poison gas, Corrosive]; Ammonia, puriss., anhydrous, >=99.9%; Ammonia solution 0.25M in tetrahydrofuran; Ammonia, puriss., anhydrous, >=99.95%; E-527; Q4087; R-717; C00014; D02916; Dowex(R) Marathon(TM) WBA free base, free base; Q4832241; Q6004010; Q27110025; (Aminomethyl)polystyrene, 100-200 mesh, extent of labeling: ~2 mmol/g amine loading; (Aminomethyl)polystyrene, 200-400 mesh, extent of labeling: ~0.6 mmol/g amine loading; (Aminomethyl)polystyrene, 200-400 mesh, extent of labeling: ~1.5 mmol/g amine loading; (Aminomethyl)polystyrene, 400-500 mum, extent of labeling: 1-2 mmol/g amine loading; (Aminomethyl)polystyrene, 100-200 mesh, extent of labeling: 0.5-1.0 mmol/g N loading, 1 % cross-linked; (Aminomethyl)polystyrene, 100-200 mesh, extent of labeling: 1.0 mmol/g N loading, 1 % cross-linked; (Aminomethyl)polystyrene, 200-400 mesh, extent of labeling: 1.0-1.5 mmol/g N loading, 1 % cross-linked; (Aminomethyl)polystyrene, 200-400 mesh, extent of labeling: 1.0-2.0 mmol/g loading, 2 % cross-linked; (Aminomethyl)polystyrene, 200-400 mesh, extent of labeling: 4.0 mmol/g loading, 2 % cross-linked; (Aminomethyl)polystyrene, 50-100 mesh, extent of labeling: 2.0 mmol/g loading, 1 % cross-linked; (Aminomethyl)polystyrene, 70-90 mesh, extent of labeling: 1.0-1.5 mmol/g N loading, 1 % cross-linked; (Aminomethyl)polystyrene, 70-90 mesh, extent of labeling: 1.5-2.0 mmol/g N loading, 1 % cross-linked; (Aminomethyl)polystyrene, macroporous, 30-60 mesh, extent of labeling: 1.5-3.0 mmol/g loading; (Aminomethyl)polystyrene, macroporous, 70-90 mesh, extent of labeling: 1.5-3.0 mmol/g loading; Ammonia (includes anhydrous ammonia and aqueous ammonia from water dissociable ammonium salts and other sources 10% of total aqueous ammonia is reportable under this listing); Ammonia, anhydrous, liquefied or ammonia solutions, relative density <0.880 at 15 C in water, with >50% ammonia; Ammonia, anhydrous, liquefied or ammonia solutions, relative density <0.880 at 15 C in water, with >50% ammonia [UN1005] [Nonflammable gas]; Ammonia, anhydrous, liquefied or ammonia solutions, relative density <0.880 at 15 C in water, with >50% ammonia [UN1005] [Poison gas, Corrosive]; StratoSpheres(TM) PL-AMS resin, 100-200 mesh, extent of labeling: ~1.0 mmol/g loading, 1 % cross-linked with divinylbenzene; StratoSpheres(TM) PL-AMS resin, 100-200 mesh, extent of labeling: 2.0 mmol/g loading, 1 % cross-linked; StratoSpheres(TM) PL-AMS resin, 30-40 mesh, extent of labeling: 1.0 mmol/g loading, 1 % cross-linked; StratoSpheres(TM) PL-AMS resin, 30-40 mesh, extent of labeling: 2.0 mmol/g loading, 1 % cross-linked; StratoSpheres(TM) PL-AMS resin, 50-100 mesh, extent of labeling: 2.0 mmol/g loading, 1 % cross-linked
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  Formula H3N
  Weight 17.031
  Structure Could Not Find 2D Structure
3D Structure Download 2D Structure Download
  InChI InChI=1S/H3N/h1H3
  InChI Key QGZKDVFQNNGYKY-UHFFFAOYSA-N
  Isomeric SMILES N
  Canonical SMILES N
  External Links PubChem ID 222
CAS ID 7664-41-7
CHEMBL ID CHEMBL1160819
  NP Activity Charts   Click to show/hide
  Activity Info  

 The Content Variation of Natural Product Induced by Different Factor(s)
      Species Name: Actinomadura glauciflava strain S4215
  Factor Name: Peptone water [1]
              Species Info Factor Info
               Experiment Detail
Healthy leaf, shoot and root tissues of Eaglewood (Aquilaria crassna Pierre ex Lec.) were collected from the plantations in Nakhonnayok province (14° 7′ 20.60″ N, 101° 4′ 16.23″ E) and Phetchabun province (16° 25′ 27.59″ N, 101° 9′ 42.25″ E) of Thailand, during the period of September-October 2008. The actinomycetes isolates were grown on HT agar at 30 ℃ for 3 weeks. Four-millimeter-diameter agar plugs were cut with a sterile cork borer from the leading edges of colonies, and one such plug was transferred into a 250 ml Erlenmeyer flask containing 100 ml of ISP-2 broth and incubated at 30 ℃ for 3 weeks for preparation of seed culture. One percent of seed culture was propagated in ISP-2 broth supplemented with 0.2% L-tryptophan and incubated in the dark at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in peptone water and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in modified Gaus No.1 broth and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. Catechol-type siderophores were determined by using Arnow's method (Arnow 1937) and hydroxamate siderophores were determined by using the Csaky test (Csaky 1984).
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               Factor Part Location NP Content
 
Peptone water (30℃ + 21 days)
 Healthy leaves, shoots and root tissues Nakhonnayok province and Phetchabun province, Thailand
NP Content: 7 mg/ml
      Species Name: Kibdelosporangium sp. S4312
  Factor Name: Peptone water [1]
              Species Info Factor Info
               Experiment Detail
Healthy leaf, shoot and root tissues of Eaglewood (Aquilaria crassna Pierre ex Lec.) were collected from the plantations in Nakhonnayok province (14° 7′ 20.60″ N, 101° 4′ 16.23″ E) and Phetchabun province (16° 25′ 27.59″ N, 101° 9′ 42.25″ E) of Thailand, during the period of September-October 2008. The actinomycetes isolates were grown on HT agar at 30 ℃ for 3 weeks. Four-millimeter-diameter agar plugs were cut with a sterile cork borer from the leading edges of colonies, and one such plug was transferred into a 250 ml Erlenmeyer flask containing 100 ml of ISP-2 broth and incubated at 30 ℃ for 3 weeks for preparation of seed culture. One percent of seed culture was propagated in ISP-2 broth supplemented with 0.2% L-tryptophan and incubated in the dark at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in peptone water and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in modified Gaus No.1 broth and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. Catechol-type siderophores were determined by using Arnow's method (Arnow 1937) and hydroxamate siderophores were determined by using the Csaky test (Csaky 1984).
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               Factor Part Location NP Content
 
Peptone water (30℃ + 21 days)
 Healthy leaves, shoots and root tissues Nakhonnayok province and Phetchabun province, Thailand
NP Content: 2 mg/ml
      Species Name: Nocardia alba strain S4301
  Factor Name: Peptone water [1]
              Species Info Factor Info
               Experiment Detail
Healthy leaf, shoot and root tissues of Eaglewood (Aquilaria crassna Pierre ex Lec.) were collected from the plantations in Nakhonnayok province (14° 7′ 20.60″ N, 101° 4′ 16.23″ E) and Phetchabun province (16° 25′ 27.59″ N, 101° 9′ 42.25″ E) of Thailand, during the period of September-October 2008. The actinomycetes isolates were grown on HT agar at 30 ℃ for 3 weeks. Four-millimeter-diameter agar plugs were cut with a sterile cork borer from the leading edges of colonies, and one such plug was transferred into a 250 ml Erlenmeyer flask containing 100 ml of ISP-2 broth and incubated at 30 ℃ for 3 weeks for preparation of seed culture. One percent of seed culture was propagated in ISP-2 broth supplemented with 0.2% L-tryptophan and incubated in the dark at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in peptone water and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in modified Gaus No.1 broth and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. Catechol-type siderophores were determined by using Arnow's method (Arnow 1937) and hydroxamate siderophores were determined by using the Csaky test (Csaky 1984).
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               Factor Part Location NP Content
 
Peptone water (30℃ + 21 days)
 Healthy leaves, shoots and root tissues Nakhonnayok province and Phetchabun province, Thailand
NP Content: 20 mg/ml
      Species Name: Nocardia jiangxiensis strain S3308
  Factor Name: Peptone water [1]
              Species Info Factor Info
               Experiment Detail
Healthy leaf, shoot and root tissues of Eaglewood (Aquilaria crassna Pierre ex Lec.) were collected from the plantations in Nakhonnayok province (14° 7′ 20.60″ N, 101° 4′ 16.23″ E) and Phetchabun province (16° 25′ 27.59″ N, 101° 9′ 42.25″ E) of Thailand, during the period of September-October 2008. The actinomycetes isolates were grown on HT agar at 30 ℃ for 3 weeks. Four-millimeter-diameter agar plugs were cut with a sterile cork borer from the leading edges of colonies, and one such plug was transferred into a 250 ml Erlenmeyer flask containing 100 ml of ISP-2 broth and incubated at 30 ℃ for 3 weeks for preparation of seed culture. One percent of seed culture was propagated in ISP-2 broth supplemented with 0.2% L-tryptophan and incubated in the dark at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in peptone water and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in modified Gaus No.1 broth and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. Catechol-type siderophores were determined by using Arnow's method (Arnow 1937) and hydroxamate siderophores were determined by using the Csaky test (Csaky 1984).
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               Factor Part Location NP Content
 
Peptone water (30℃ + 21 days)
 Healthy leaves, shoots and root tissues Nakhonnayok province and Phetchabun province, Thailand
NP Content: 30 mg/ml
      Species Name: Nocardia jiangxiensis strain S3311
  Factor Name: Peptone water [1]
              Species Info Factor Info
               Experiment Detail
Healthy leaf, shoot and root tissues of Eaglewood (Aquilaria crassna Pierre ex Lec.) were collected from the plantations in Nakhonnayok province (14° 7′ 20.60″ N, 101° 4′ 16.23″ E) and Phetchabun province (16° 25′ 27.59″ N, 101° 9′ 42.25″ E) of Thailand, during the period of September-October 2008. The actinomycetes isolates were grown on HT agar at 30 ℃ for 3 weeks. Four-millimeter-diameter agar plugs were cut with a sterile cork borer from the leading edges of colonies, and one such plug was transferred into a 250 ml Erlenmeyer flask containing 100 ml of ISP-2 broth and incubated at 30 ℃ for 3 weeks for preparation of seed culture. One percent of seed culture was propagated in ISP-2 broth supplemented with 0.2% L-tryptophan and incubated in the dark at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in peptone water and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in modified Gaus No.1 broth and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. Catechol-type siderophores were determined by using Arnow's method (Arnow 1937) and hydroxamate siderophores were determined by using the Csaky test (Csaky 1984).
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               Factor Part Location NP Content
 
Peptone water (30℃ + 21 days)
 Healthy leaves, shoots and root tissues Nakhonnayok province and Phetchabun province, Thailand
NP Content: 25 mg/ml
      Species Name: Nonomuraea rubra strain S3304
  Factor Name: Peptone water [1]
              Species Info Factor Info
               Experiment Detail
Healthy leaf, shoot and root tissues of Eaglewood (Aquilaria crassna Pierre ex Lec.) were collected from the plantations in Nakhonnayok province (14° 7′ 20.60″ N, 101° 4′ 16.23″ E) and Phetchabun province (16° 25′ 27.59″ N, 101° 9′ 42.25″ E) of Thailand, during the period of September-October 2008. The actinomycetes isolates were grown on HT agar at 30 ℃ for 3 weeks. Four-millimeter-diameter agar plugs were cut with a sterile cork borer from the leading edges of colonies, and one such plug was transferred into a 250 ml Erlenmeyer flask containing 100 ml of ISP-2 broth and incubated at 30 ℃ for 3 weeks for preparation of seed culture. One percent of seed culture was propagated in ISP-2 broth supplemented with 0.2% L-tryptophan and incubated in the dark at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in peptone water and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in modified Gaus No.1 broth and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. Catechol-type siderophores were determined by using Arnow's method (Arnow 1937) and hydroxamate siderophores were determined by using the Csaky test (Csaky 1984).
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               Factor Part Location NP Content
 
Peptone water (30℃ + 21 days)
 Healthy leaves, shoots and root tissues Nakhonnayok province and Phetchabun province, Thailand
NP Content: 3 mg/ml
      Species Name: Nonomuraea sp. S3310
  Factor Name: Peptone water [1]
              Species Info Factor Info
               Experiment Detail
Healthy leaf, shoot and root tissues of Eaglewood (Aquilaria crassna Pierre ex Lec.) were collected from the plantations in Nakhonnayok province (14° 7′ 20.60″ N, 101° 4′ 16.23″ E) and Phetchabun province (16° 25′ 27.59″ N, 101° 9′ 42.25″ E) of Thailand, during the period of September-October 2008. The actinomycetes isolates were grown on HT agar at 30 ℃ for 3 weeks. Four-millimeter-diameter agar plugs were cut with a sterile cork borer from the leading edges of colonies, and one such plug was transferred into a 250 ml Erlenmeyer flask containing 100 ml of ISP-2 broth and incubated at 30 ℃ for 3 weeks for preparation of seed culture. One percent of seed culture was propagated in ISP-2 broth supplemented with 0.2% L-tryptophan and incubated in the dark at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in peptone water and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in modified Gaus No.1 broth and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. Catechol-type siderophores were determined by using Arnow's method (Arnow 1937) and hydroxamate siderophores were determined by using the Csaky test (Csaky 1984).
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               Factor Part Location NP Content
 
Peptone water (30℃ + 21 days)
 Healthy leaves, shoots and root tissues Nakhonnayok province and Phetchabun province, Thailand
NP Content: 9 mg/ml
      Species Name: Pseudonocardia halophobica strain S4201
  Factor Name: Peptone water [1]
              Species Info Factor Info
               Experiment Detail
Healthy leaf, shoot and root tissues of Eaglewood (Aquilaria crassna Pierre ex Lec.) were collected from the plantations in Nakhonnayok province (14° 7′ 20.60″ N, 101° 4′ 16.23″ E) and Phetchabun province (16° 25′ 27.59″ N, 101° 9′ 42.25″ E) of Thailand, during the period of September-October 2008. The actinomycetes isolates were grown on HT agar at 30 ℃ for 3 weeks. Four-millimeter-diameter agar plugs were cut with a sterile cork borer from the leading edges of colonies, and one such plug was transferred into a 250 ml Erlenmeyer flask containing 100 ml of ISP-2 broth and incubated at 30 ℃ for 3 weeks for preparation of seed culture. One percent of seed culture was propagated in ISP-2 broth supplemented with 0.2% L-tryptophan and incubated in the dark at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in peptone water and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in modified Gaus No.1 broth and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. Catechol-type siderophores were determined by using Arnow's method (Arnow 1937) and hydroxamate siderophores were determined by using the Csaky test (Csaky 1984).
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               Factor Part Location NP Content
 
Peptone water (30℃ + 21 days)
 Healthy leaves, shoots and root tissues Nakhonnayok province and Phetchabun province, Thailand
NP Content: 30 mg/ml
      Species Name: Streptomyces hainanensis strain S4303
  Factor Name: Peptone water [1]
              Species Info Factor Info
               Experiment Detail
Healthy leaf, shoot and root tissues of Eaglewood (Aquilaria crassna Pierre ex Lec.) were collected from the plantations in Nakhonnayok province (14° 7′ 20.60″ N, 101° 4′ 16.23″ E) and Phetchabun province (16° 25′ 27.59″ N, 101° 9′ 42.25″ E) of Thailand, during the period of September-October 2008. The actinomycetes isolates were grown on HT agar at 30 ℃ for 3 weeks. Four-millimeter-diameter agar plugs were cut with a sterile cork borer from the leading edges of colonies, and one such plug was transferred into a 250 ml Erlenmeyer flask containing 100 ml of ISP-2 broth and incubated at 30 ℃ for 3 weeks for preparation of seed culture. One percent of seed culture was propagated in ISP-2 broth supplemented with 0.2% L-tryptophan and incubated in the dark at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in peptone water and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in modified Gaus No.1 broth and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. Catechol-type siderophores were determined by using Arnow's method (Arnow 1937) and hydroxamate siderophores were determined by using the Csaky test (Csaky 1984).
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               Factor Part Location NP Content
 
Peptone water (30℃ + 21 days)
 Healthy leaves, shoots and root tissues Nakhonnayok province and Phetchabun province, Thailand
NP Content: 60 mg/ml
      Species Name: Streptomyces javensis strain S4202
  Factor Name: Peptone water [1]
              Species Info Factor Info
               Experiment Detail
Healthy leaf, shoot and root tissues of Eaglewood (Aquilaria crassna Pierre ex Lec.) were collected from the plantations in Nakhonnayok province (14° 7′ 20.60″ N, 101° 4′ 16.23″ E) and Phetchabun province (16° 25′ 27.59″ N, 101° 9′ 42.25″ E) of Thailand, during the period of September-October 2008. The actinomycetes isolates were grown on HT agar at 30 ℃ for 3 weeks. Four-millimeter-diameter agar plugs were cut with a sterile cork borer from the leading edges of colonies, and one such plug was transferred into a 250 ml Erlenmeyer flask containing 100 ml of ISP-2 broth and incubated at 30 ℃ for 3 weeks for preparation of seed culture. One percent of seed culture was propagated in ISP-2 broth supplemented with 0.2% L-tryptophan and incubated in the dark at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in peptone water and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. One percent of seed culture was propagated in modified Gaus No.1 broth and incubated at 30 ℃ with shaking at 120 rev/min for 3 weeks. Catechol-type siderophores were determined by using Arnow's method (Arnow 1937) and hydroxamate siderophores were determined by using the Csaky test (Csaky 1984).
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               Factor Part Location NP Content
 
Peptone water (30℃ + 21 days)
 Healthy leaves, shoots and root tissues Nakhonnayok province and Phetchabun province, Thailand
NP Content: 30 mg/ml
References
1 Endophytic actinomycetes isolated from Aquilaria crassna Pierre ex Lec and screening of plant growth promoters production