(+)-Borneol - Moligand™, analytical standard, ≥98%(GC) , Activator of TRPV3, CAS No.464-43-7, Activator of TRPV3

CAS: 464-43-7 Cat. No.: B109562 Peso molecular: 154.25 Beilstein Registry Number: 2038056 Número EC: 207-352-6

GRADE & PURITY Analytical standard, Moligand™, ≥98%(GC)

Synonyms

AC-5982 | BS-42578 | D-BORNEOL [WHO-DD] | Pain relief patch-acupoint pressure stimulation | (1R-endo)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol | BORNEOL, D- | BRN 2038056 | Endo-2-camphanol | endo-1,7,7-Trimethylbicyclo | (1R-endo)-1,7,7-Trimethylbicyclo(

Storage

Store at 2-8°C

Shipped In

Wet ice

Descripción general

(+)-Borneol, a bicyclic monoterpene, is found in the essential oils of medicinal plants and is commonly used in traditional Chinese medicine for analgesia and anaesthesia.
(+)-Borneol has been used to study its antiapoptotic, antioxidative and neuroprotective effect in human neuroblastoma cells (SH-SY5Y).

Specifications

Sinónimos

AC-5982 | BS-42578 | D-BORNEOL [WHO-DD] | Pain relief patch-acupoint pressure stimulation | (1R-endo)-1, 7, 7-trimethylbicyclo[2.2.1]heptan-2-ol | BORNEOL, D- | BRN 2038056 | Endo-2-camphanol | endo-1, 7, 7-Trimethylbicyclo | (1R-endo)-1, 7, 7-Trimethylbicyclo(

Especificaciones y pureza

Moligand™, analytical standard, ≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Grado

Analytical standard, Moligand™

Tipo de acción

ACTIVATOR

Mecanismo de acción

Activator of TRPV3

Pureza

≥98%(GC)

Nombres e identificadores

• Sonrisas canónicas: CC1(C2CCC1(C(C2)O)C)C
• IUPAC Name: (1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
• InChIKey: DTGKSKDOIYIVQL-WEDXCCLWSA-N
• INCHI: 1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8+,10+/m1/s1
• Isómeros SMILES: C[C@@]12CC[C@@H](C1(C)C)C[C@@H]2O
• WGK Alemania: 3
• RTECS: ED7060000
• Número ONU: 1312
• Grupo de embalaje: III
• Peso molecular: 154.25
• Beilstein: 2038056
• Reaxy-Rn: 6052111
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6052111&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Prenol lipids
      • Subclass Monoterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Prenol lipids
• Subclass: Monoterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Bicyclic monoterpenoids
• Alternative Parents: Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Bicyclic monoterpenoid - Bornane monoterpenoid - Cyclic alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homopolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
• External Descriptors: borneol

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

Objetivos asociados (humanos)

TRPV3 Tchem Transient receptor potential cation channel subfamily V member 3 (1 Activities)

Discover Target: TRPV3

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Objetivos asociados (no humanos)

Colletotrichum fragariae (147 Activities)

Explore this target

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

Colletotrichum gloeosporioides (560 Activities)

Explore this target

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

Mecanismos de acción

Propiedades químicas y físicas

• Rotación específica [α]: +36°, c = 5 in ethanol
• Punto de inflamación (°F): 149 °F
• Punto de inflamación (°C): 65 °C
• Punto de fusión (°C): 206-209°C
• Peso molecular: 154.250 g/mol
• XLogP3: 2.700
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 154.136 Da
• Monoisotopic Mass: 154.136 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 185.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Huijuan Li, Xinghui Song, Huiru Li, Lifei Zhu, Shengbo Cao, Jifeng Liu.  (2022)  Sesquiterpenes and Monoterpenes from the Leaves and Stems of Illicium simonsii and Their Antibacterial Activity.  MOLECULES,  27  (3): (1115).  [PMID:35164380] [10.3390/molecules27031115]

2. Jingwei Liu, Tong Shu, Yiheng Mu, Wanlin Zheng, Xiaohuan Lu, Hong Tao.  (2025)  Curdione combined with borneol treats bacterial mixed HPV infection by regulating the crosstalk among immune cells.  Frontiers in Immunology,      [PMID:39911394] [10.3389/fimmu.2025.1503355]