General Information of Natural Product (ID: NP0791)
  Natural Product Name
Myristicin
  Synonyms
Myristicin; 607-91-0; Myristicine; 6-Allyl-4-methoxy-1,3-benzodioxole; Myristicin (6CI); 4-Methoxy-6-(2-propenyl)-1,3-benzodioxole; 5-Allyl-1-methoxy-2,3-(methylenedioxy)benzene; UNII-04PD6CT78W; 1,3-Benzodioxole, 4-methoxy-6-(2-propenyl)-; Benzene, 5-allyl-1-methoxy-2,3-(methylenedioxy)-; CHEBI:68234; 5-Allyl-2,3-(methylendioxy)anisole; 6-allyl-4-methoxybenzo[d][1,3]dioxole; 04PD6CT78W; 4-Methoxy-6-[2-propenyl]-1,3-benzodioxole; Myristicin from parsley leaf oil; MFCD00133549; 4-methoxy-6-(prop-2-en-1-yl)-2H-1,3-benzodioxole; 1,3-Benzodioxole, 4-methoxy-6-(2-propenyl)- (9CI); CCRIS 6782; HSDB 3516; EINECS 210-146-9; BRN 0166218; 4-methoxy-6-prop-2-enyl-1,3-benzodioxole; DSSTox_CID_5693; DSSTox_RID_77884; DSSTox_GSID_25693; SCHEMBL68041; 5-19-02-00631 (Beilstein Handbook Reference); MLS001065535; Myristicin, analytical standard; CHEMBL481044; DTXSID1025693; HMS2270K14; ZINC403089; HY-N2510; Tox21_200172; BDBM50242966; s3291; STK693140; 6-allyl-4-methoxy-benzo-1,3-dioxole; AKOS005604763; CCG-208543; MCULE-6209105333; NCGC00091427-01; NCGC00091427-02; NCGC00257726-01; AC-34678; CAS-607-91-0; SMR000112534; 1-Allyl-3-methoxy-4,5-methylenedioxybenzene; CS-0022781; FT-0672575; V0156; C10480; 5-Allyl-1-methoxy-2,3-(methylenedioxy)-Benzene; 4-methoxy-6-(prop-2-en-1-yl)-1,3-benzodioxole; 607M910; Q414057; SR-01000838340; 4-Methoxy-6-(2-propenyl)-1,3-benzodioxole, 9CI; SR-01000838340-3; 1-Methoxy-2,3-methylenedioxy-5-(2-propenyl)benzene; Myristicin from parsley leaf oil, >=85% (HPLC), oil; NCGC00091427-03!4-methoxy-6-prop-2-enyl-1,3-benzodioxole
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  Formula C11H12O3
  Weight 192.21
  Structure Could Not Find 2D Structure
3D Structure Download 2D Structure Download
  InChI InChI=1S/C11H12O3/c1-3-4-8-5-9(12-2)11-10(6-8)13-7-14-11/h3,5-6H,1,4,7H2,2H3
  InChI Key BNWJOHGLIBDBOB-UHFFFAOYSA-N
  Isomeric SMILES COC1=CC(=CC2=C1OCO2)CC=C
  Canonical SMILES COC1=CC(=CC2=C1OCO2)CC=C
  External Links PubChem ID 4276
CAS ID 607-91-0
NPASS ID NPC119949
CHEMBL ID CHEMBL481044
  NP Activity Charts   Click to show/hide

 The Content Variation of Natural Product Induced by Different Factor(s)
      Species Name: Portenschlagiella ramosissima
  Factor Name: Developmental Stage Variation [1]
              Species Info Factor Info
               Experiment Detail
Plant material was collected in October 2003. in Herceg Novi, Montenegro. The air-dried roots (54 g), seeds (73.5 g) and aerial parts during vegetative phase (V, 150 g) and aerial parts during flowering period (F, 110 g) of P. ramosissima were submitted for 3 h to water-distillation using a Clevenger type apparatus.
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               Factor Function
In all the oils samples the main component was myristicin. In the root oil myristicin was present with 68.5%, in oil from aerial parts during vegetative phase, myristicin was present with 88.9%, while in oil from aerial parts during flowering period this component was present with 91.5%, in the seed oil myristicin was found with 61.1%. It can be seen that myristicin was the most abundant component in all oil samples that we investigated with very high percentage. But, it can also be seen that the season of plant collection influenced the oil characteristics. The highest content of myristicin was present in the oil sample isolated from plants collected during the flowering period (91.5%), than in oil isolated during the vegetative phase.
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               Factor Part Location NP Content
 
Aerial parts: vegetative stage
Aerial parts Montenegro
NP Content: 88.9 %
 
Aerial parts: flowering stage
Aerial parts Montenegro
NP Content: 91.5 %
 
Root: vegetative stage
Roots Montenegro
NP Content: 68.5 %
 
Seed: vegetative stage
Seeds Montenegro
NP Content: 61.1 %
References
1 Antimicrobial Activity of Essential Oils Isolated from Different Parts of Endemic Plant Portenschlagiella ramosissima Tutin