Phytol - 10mM in DMSO , CAS No.150-86-7

CAS: 150-86-7 Cat. No.: P421785 Formula: C₂₀H₄₀O Peso molecolare: 296.54 Beilstein Registry Number: 1(2)503 Numero EC: 416-120-5 PubChem CID: 5280435

QUALITÀ & PUREZZA 10mM in DMSO

Synonyms

EINECS 205-776-6 | UNII-MZQ4XE15TP | MFCD00151280 | SCHEMBL22783 | (E,R,R)-PHYTOL | C01389 | P0411 | Phytol | EN300-18543961 | HY-N3075 | (7R,11R,2E)-PHYTOL | (2E)(7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol | EF32FF86-42DC-475E-935A-5C0AE6F1CAA0 | Phy

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Panoramica

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)

Specifiche

Sinonimi

EINECS 205-776-6 | UNII-MZQ4XE15TP | MFCD00151280 | SCHEMBL22783 | (E,R,R)-PHYTOL | C01389 | P0411 | Phytol | EN300-18543961 | HY-N3075 | (7R,11R,2E)-PHYTOL | (2E)(7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol | EF32FF86-42DC-475E-935A-5C0AE6F1CAA0 | Phy

Specifiche e purezza

10mM in DMSO

Meccanismi biochimici e fisiologici

Phytol has potential anti-schistosome properties. It induces sedative and anxiolytic effects in mice.

Condizioni di conservazione di stoccaggio

Store at -80°C

Spedito in

Dry ice packs + Cold packs

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Tipo di azione

INHIBITOR

Nomi e identificatori

Pubchem Sid

528772261

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528772261

Sorrisi canonici

CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C

IUPAC Name

(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol

InChIKey

BOTWFXYSPFMFNR-PYDDKJGSSA-N

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

Isomeri SMILES

C[C@@H](CCC[C@@H](C)CCC/C(=C/CO)/C)CCCC(C)C

RTECS

TJ3490000

PubChem CID

5280435

Peso molecolare

296.54

Beilstein

1(2)503

Reaxy-Rn

7855349

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Prenol lipids
      • Subclass Diterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: 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
• Descrizione: 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

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

PTPN2 Tchem T-cell protein-tyrosine phosphatase (1317 Activities)

Discover Target: PTPN2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTPN6 Tchem Protein-tyrosine phosphatase 1C (687 Activities)

Discover Target: PTPN6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTPN11 Tchem Protein-tyrosine phosphatase 2C (2297 Activities)

Discover Target: PTPN11

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTPRF Tchem Receptor-type tyrosine-protein phosphatase F (LAR) (718 Activities)

Discover Target: PTPRF

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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)

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SW-620 (52400 Activities)

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HCT-15 (51914 Activities)

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Obiettivi associati (non umani)

Cdc25b Dual specificity phosphatase Cdc25B (32 Activities)

Discover Target: Cdc25b

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Ptpn1 Protein-tyrosine phosphatase 1B (270 Activities)

Discover Target: Ptpn1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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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Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: air sensitive
• Indice di rifrazione: 1.463
• Punto di infiammabilità (°F): 368.6 °F
• Punto di infiammabilità (°C): 187 °C
• Punto di ebollizione (°C): 202-204 °C/10 mmHg
• Peso molecolare: 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