(+)-Borneol - Moligand™, 10mM in DMSO , Activator of TRPV3, CAS No.464-43-7, Activator of TRPV3

CAS: 464-43-7 Cat. No.: B424091 Summenformel: C₁₀H₁₈O Molekulargewicht: 154.25 Beilstein Registry Number: 2038056 EG-Nummer: 207-352-6

GRADE & PURITY Moligand™, 10mM in DMSO

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 -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

(+)-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

Synonyme

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(

Spezifikationen & Reinheit

Moligand™, 10mM in DMSO

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Note

Moligand™

Aktionsart

ACTIVATOR

Mechanismus der Wirkung

Activator of TRPV3

Namen und Kennungen

• Pubchem Sid: 528752690
• Isomere SMILES: C[C@@]12CC[C@@H](C1(C)C)C[C@@H]2O
• WGK Deutschland: 3
• RTECS: ED7060000
• UN-Nummer: 1312
• Verpackungsgruppe: III
• Molekulargewicht: 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=

Zugehörige Ziele (menschlich)

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)

Zugehörige Ziele (nicht menschlich)

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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Spezifische Drehung [α]: +36°, c = 5 in ethanol
• Flammpunkt (°F): 149 °F
• Flammpunkt (°C): 65 °C
• Schmelzpunkt (°C): 206-209°C
• Molekulargewicht: 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

Referenzen

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]