PMD38 - Moligand™ , Activator of TRPM8, CAS No.91739-72-9, Activator of TRPM8

CAS: 91739-72-9 Cat. No.: P612879 EG-Nummer: 622-019-9 PubChem CID: 19100

GRADE & PURITY Moligand™

Synonyms

(1R,3R,4R)-2-hydroxy-alpha,alpha,4-trimethylcyclohexanemethanol | AAL436QJ5W | GTPL2472 | 1beta,3beta,4alpha--p-menthane-3,8-diol | 1beta,3beta,4alpha-p-menthane-3,8-diol | 3,8-P-MENTHANEDIOL, (-)- | AKOS037646772 | Cyclohexanemethanol, 2-hydroxy-.alpha.,

Storage

Room temperature

Specifications

Synonyme

(1R,3R,4R)-2-hydroxy-alpha,alpha,4-trimethylcyclohexanemethanol | AAL436QJ5W | GTPL2472 | 1beta,3beta,4alpha--p-menthane-3,8-diol | 1beta,3beta,4alpha-p-menthane-3,8-diol | 3,8-P-MENTHANEDIOL, (-)- | AKOS037646772 | Cyclohexanemethanol, 2-hydroxy-.alpha.,

Spezifikationen & Reinheit

Moligand™

Storage

Room temperature

Note

Moligand™

Aktionsart

ACTIVATOR

Mechanismus der Wirkung

Activator of TRPM8

Namen und Kennungen

Kanonisches Lächeln

C[C@@H]1CC[C@H]([C@@H](C1)O)C(O)(C)C

IUPAC Name

(1R,2R,5R)-2-(2-hydroxypropan-2-yl)-5-methylcyclohexan-1-ol

InChIKey

LMXFTMYMHGYJEI-IWSPIJDZSA-N

INCHI

1S/C10H20O2/c1-7-4-5-8(9(11)6-7)10(2,3)12/h7-9,11-12H,4-6H2,1-3H3/t7-,8-,9-/m1/s1

Isomere SMILES

C[C@@H]1CC[C@H]([C@@H](C1)O)C(C)(C)O

PubChem CID

19100

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Klasse: Prenol lipids
• Subclass: Monoterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Menthane monoterpenoids
• Alternative Parents: Monocyclic monoterpenoids Cyclohexanols Tertiary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: P-menthane monoterpenoid - Monocyclic monoterpenoid - Cyclohexanol - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.
• External Descriptors: Menthane monoterpenoids

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

Zugehörige Ziele (menschlich)

TRPM8 Tclin Transient receptor potential cation channel subfamily M member 8 (1 Activities)

Discover Target: TRPM8

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

Chemische und physikalische Eigenschaften

• Molekulargewicht: 172.260 g/mol
• XLogP3: 2.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 172.146 Da
• Monoisotopic Mass: 172.146 Da
• Topological Polar Surface Area: 40.500 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 154.000
• 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