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Basic Description
| Synonyms | Phytol | 150-86-7 | trans-Phytol | (E)-Phytol | 2-Hexadecen-1-ol, 3,7,11,15-tetramethyl-, (2E,7R,11R)- | CHEBI:17327 | (E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol | (2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecen-1-ol | UNII-MZQ4XE15TP | MZQ4XE15TP | EINECS 205-776-6 | BRN |
|---|---|
| Specifications & Purity | 10mM in DMSO |
| Biochemical and Physiological Mechanisms | Phytol has potential anti-schistosome properties. It induces sedative and anxiolytic effects in mice. |
| Storage Temp | Store at -80°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
Chlorophyll alcohol is a diterpene alcohol, which is usually used as an aromatic component in various aromatic compounds. It has been found that it is a component of chlorophyll, vitamin K, vitamin E and other tocopherols in nature. Some lipophilic analogues have strong antituberculosis activity. Phytol was used to study the EAG responses of male and female potato tuber moths to various plant volatiles. It is used to synthesize propiolic acid (2,6,10,14- tetramethylpentadecanoic acid) |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Lipids and lipid-like molecules
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Class
Prenol lipids
- Subclass Diterpenoids
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Class
Prenol lipids
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Superclass
Lipids and lipid-like molecules
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Prenol lipids |
| Subclass | Diterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acyclic diterpenoids |
| Alternative Parents | Long-chain fatty alcohols Primary alcohols Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acyclic diterpenoid - Long chain fatty alcohol - Fatty alcohol - Fatty acyl - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as acyclic diterpenoids. These are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle. |
| External Descriptors | Acyclic diterpenoids |
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Associated Targets(Human)
PTPN2
Tchem
T-cell protein-tyrosine phosphatase (1317 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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PTPN6
Tchem
Protein-tyrosine phosphatase 1C (687 Activities)
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PTPN11
Tchem
Protein-tyrosine phosphatase 2C (2297 Activities)
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PTPRF
Tchem
Receptor-type tyrosine-protein phosphatase F (LAR) (718 Activities)
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K562 (73714 Activities)
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MCF7 (126967 Activities)
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U-251 (51189 Activities)
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U-87 MG (3946 Activities)
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A549 (127892 Activities)
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HeLa (62764 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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SW-620 (52400 Activities)
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HCT-15 (51914 Activities)
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Associated Targets(non-human)
Cdc25b
Dual specificity phosphatase Cdc25B (32 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Ptpn1
Protein-tyrosine phosphatase 1B (270 Activities)
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Staphylococcus aureus (210822 Activities)
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Escherichia coli (133304 Activities)
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Mycobacterium tuberculosis (203094 Activities)
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Mus musculus (284745 Activities)
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C3H 10T1/2 (488 Activities)
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Names and Identifiers
| IUPAC Name | (E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol |
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| INCHI | InChI=1S/C20H40O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h15,17-19,21H,6-14,16H2,1-5H3/b20-15+/t18-,19-/m1/s1 |
| InChIKey | BOTWFXYSPFMFNR-PYDDKJGSSA-N |
| Smiles | CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C |
| Isomeric SMILES | C[C@@H](CCC[C@@H](C)CCC/C(=C/CO)/C)CCCC(C)C |
| RTECS | TJ3490000 |
| PubChem CID | 5280435 |
| Molecular Weight | 296.54 |
| Beilstein | 1(2)503 |
| Reaxy-Rn | 7855349 |
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
| Sensitivity | air sensitive |
|---|---|
| Refractive Index | 1.463 |
| Flash Point(°F) | 368.6 °F |
| Flash Point(°C) | 187 °C |
| Boil Point(°C) | 202-204 °C/10 mmHg |
| Molecular Weight | 296.500 g/mol |
| XLogP3 | 8.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 13 |
| Exact Mass | 296.308 Da |
| Monoisotopic Mass | 296.308 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 255.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |
Citations of This Product
| 1. Fangchao Cui, Liqing Xi, Dangfeng Wang, Xiqian Tan, Jianrong Li, Tingting Li. (2023) High-Release, Residue-Free Polysaccharide Hydrogel for Refrigerated Food Preservation. ACS Applied Materials & Interfaces, 15 (4): (6035–6046). |
| 2. Liping Du, Chao Wang, Chenxia Zhang, Lijuan Ma, Yongquan Xu, Dongguang Xiao. (2019) Characterization of the volatile and sensory profile of instant Pu-erh tea using GC × GC-TOFMS and descriptive sensory analysis. MICROCHEMICAL JOURNAL, 146 (986). |
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