AI & ChatGPT searches , social queriess for CB2
Search references for CB2. Phrases containing CB2
See searches and references containing CB2!
Search references for CB2. Phrases containing CB2
See searches and references containing CB2!CB2
Topics referred to by the same term
CB2 or similar, may refer to: Cannabinoid receptor type 2 Crash Bandicoot 2: Cortex Strikes Back, a video game developed by Naughty Dog for PlayStation
CB2
Group of receptors to cannabinoid compounds
and CB2. The CB1 receptor is expressed mainly in the brain (central nervous system or "CNS"), but also in the lungs, liver and kidneys. The CB2 receptor
Cannabinoid_receptor
Mammalian protein found in Homo sapiens
The cannabinoid receptor 2 (CB2), is a G protein-coupled receptor from the cannabinoid receptor family that in humans is encoded by the CNR2 gene. It
Cannabinoid_receptor_2
American rock musician (born 1964)
Barrel CB2 Furniture Line Is Kind of Great". www.yahoo.com. Retrieved September 11, 2015.[dead link] "CB2 x Kravitz Design Furniture & Home Decor". CB2. Archived
Lenny_Kravitz
Compounds found in cannabis
patterns. A subpopulation of microglia in the human cerebellum expresses CB2. CB2 receptors are linked to immunomodulatory effects and potential therapeutic
Cannabinoid
International home decor company
"Crate and Barrel's CB2 chain takes Manhattan". Reuters. Retrieved February 5, 2010. Crate and Barrel opens its first New York-based CB2 store on Tuesday
Crate_&_Barrel
Chemical compound
be a mild cannabinoid agonist with low binding affinity for both CB1 and CB2. A study conducted in 2023 by researchers from Ben-Gurion University of the
3,3'-Diindolylmethane
Chemical compound
potent agonist of the CB2 receptor, with an EC50 of 0.52nM at CB2, and ~30x selectivity over CB1 (Ki of 110nM at CB1 vs 3.7nM at CB2). It has been sold online
MCHB-1
Natural bicyclic sesquiterpene
cannabinoid receptor type 2 (CB2 receptor). In other basic studies, β-caryophyllene has a binding affinity of Ki = 155 nM at the CB2 receptors. β-Caryophyllene
Caryophyllene
Psychoactive component of cannabis
spasticity and neuropathic pain. THC acts as a partial agonist at CB1 and CB2 cannabinoid receptors. THC can be administered orally, inhaled, or transdermally
Tetrahydrocannabinol
Substances synthesized by John W. Huffman's research group
for the cannabinoid receptor type 1 (CB1) or cannabinoid receptor type 2 (CB2). Manera C, Tuccinardi T, Martinelli A (2008). "Indoles and related compounds
List_of_JWH_cannabinoids
Chemical compound
cannabinoid receptor full agonist at both the CB1 and CB2 receptors, with a Ki of 12 nM at CB1 and 0.21 nM at CB2. Replacing the aromatic 3-benzoyl or 3-naphthoyl
A-834,735
Chemical compound
cannabinoid receptor CB2, but with much lower affinity for the psychoactive CB1 receptor. UR-144 has high affinity for the CB2 receptor with a Ki of
UR-144
Chemical compound
drug that acts as a potent and highly selective CB2 receptor inverse agonist, with a Ki of 0.6 nM at CB2 and 400 nM at the related CB1 receptor. It is used
SR-144,528
Agonist drug having partial efficacy at a receptor
falcarindiol. Delta 9-tetrahydrocannabivarin (THCV) is a partial agonist at CB2 receptors and this activity might be implicated in ∆9-THCV-mediated anti-inflammatory
Partial_agonist
Biological system of neurotransmitters
receptors have been identified: CB1, first cloned (or isolated) in 1990; and CB2, cloned in 1993. CB1 receptors are found predominantly in the brain and nervous
Endocannabinoid_system
Chemical compound
that acts as a full agonist at both the CB1 and CB2 cannabinoid receptors, with some selectivity for CB2. It produces effects in animals similar to those
JWH-018
Chemical compound (fatty acid neurotransmitter)
primarily by CB1 cannabinoid receptors in the central nervous system, and CB2 cannabinoid receptors in the periphery. The latter appear to be involved
Anandamide
Huffman, J. W. (2008). "Targeting the cannabinoid CB2 receptor: modelling and structural determinants of CB2 selective ligands". British Journal of Pharmacology
List_of_AM_cannabinoids
Naturally-occurring cannabinoid
phytocannabinoid that acts as a low affinity partial agonist at the CB1 and CB2 receptors of the endocannabinoid system (ECS). Although CBN shares the same
Cannabinol
Mammalian protein found in humans
CB1 and CB2 receptors, leading to dual anti-inflammatory and neuroprotective effects throughout the CNS. Similarly, activation of CB1 and CB2 receptors
Cannabinoid_receptor_1
Pharmaceutical compound
unlike the dimethylheptyl analogue L-759,633 which is a selective agonist for CB2 and has antiinflammatory but not psychoactive effects. Cannabidiol dimethyl
Delta-8-THCM
Cannabinoid agonist compound
Tetrahydrocannabiphorol (THCP) is a potent phytocannabinoid, a CB1 and CB2 receptor agonist which was known as a synthetic homologue of tetrahydrocannabinol
Tetrahydrocannabiphorol
Chemical compound
irritable bowel syndrome. It acts as a potent and selective cannabinoid CB2 receptor agonist and is claimed to be orally active and peripherally selective
Olorinab
Chemical compound
receptor CB2, with a Ki of 32.1 nM at CB2 and 165x selectivity over CB1, at which it acted as a weak partial agonist. It is used in the study of CB2 mediated
AM-630
Compounds that inhibit or block the activity of cannabinoid receptors
Cannabidiol (CBD), a naturally occurring cannabinoid and a non-competitive CB1/CB2 receptor antagonist, as well as Δ9-tetrahydrocannabivarin (THCV), a naturally
Cannabinoid receptor antagonist
Cannabinoid_receptor_antagonist
Chemical compound
developed by Abbott Laboratories that acts as a potent and selective cannabinoid CB2 receptor agonist. Replacing the aromatic 3-benzoyl or 3-naphthoyl group found
A-796,260
1990–1991 conflict in the Middle East
First Iraq War, 1990-1991". Purpose and Power. Shaftesbury Road, Cambridge CB2 8EA, UK: Cambridge University Press. pp. 537–559. ISBN 978-1-009-25727-5
Gulf_War
Chemical compound
for CB2, with a Ki value of 14nM at CB2 vs 19nM at CB1. It was one of the first CB2-selective ligands developed, although its selectivity for CB2 is modest
JWH-051
Chemical compound
naphthoylindole family that acts as a cannabinoid agonist at both the CB1 and CB2 receptors. It is the N-hexyl homolog of the more common synthetic cannabinoid
JWH-019
Chemical compound
which is an agonist at the cannabinoid receptors CB1 and CB2, with a CB1 Ki of 32nM and a CB2 Ki of 49nM. It is also a weak antagonist at the related receptor
PSB-SB-1202
Chemical compound
endocannabinoid because it lacks affinity for the cannabinoid receptors CB1 and CB2.[better source needed] PEA is metabolized by the cellular enzymes fatty acid
Palmitoylethanolamide
Class of chemical compounds
MYA, and a lineages that predate the evolution of CB receptors, as CB1 – CB2 duplication event may have occurred prior to the lophotrochozoan-deuterostome
N-Acylethanolamine
Pharmaceutical compound
which acts as a potent, selective and long acting agonist of the cannabinoid CB2 receptor. It was effective against neuropathic pain and allodynia in animal
LY2828360
Synthetic cannabinoid derivative drug
a potent agonist at both the CB1 and CB2 receptors, with a binding affinity of 0.1 nM at CB1 and 0.2 nM at CB2. It is mainly used in scientific research
Canbisol
Chemical compound
potent and selective agonist for the cannabinoid receptor CB2, with a Ki of 3.4 nM at CB2 and 80 times selectivity over the related CB1 receptor. It
AM-1241
Hydrogenated derivative of THC
Binding Affinities of (9R)- and (9S)-Hexahydrocannabinol (HHC) for the CB1 and CB2 Cannabinoid Receptors". ACS Chemical Biology. 20 (8): 2006–2013. doi:10.1021/acschembio
Hexahydrocannabinol
(MAGL) inhibitor Nabilone – CB1 and CB2 receptor agonist NEO-1940 – CB1 and CB2 receptor agonist Olorinab (APD-371) – CB2 receptor agonist Fasinumab (REGN-475
List of investigational analgesics
List_of_investigational_analgesics
Chemical compound
cannabinoid receptors. Affinities are: with a Ki of 1.0 nM at CB1 and 2.6 nM at CB2. The 4-methyl functional analog MAM-2201 probably has similar affinities
AM-2201
Chemical compound
CB1 receptor, with a Ki of 0.16 nM, and 26× selectivity over the related CB2 receptor. It has high potency in animal tests of cannabinoid activity, and
AM-2389
Chemical compound
selective CB2 inverse agonist. It has anti-inflammatory effects in animal studies, thought to be mediated by an interaction between the CB2 receptor and
JTE-907
Active metabolite of paracetamol
sensory neurons. AM404 is a weak agonist of cannabinoid receptors CB1 and CB2, an inhibitor of endocannabinoid transporter, a potent activator of TRPV1
AM404
Chemical compound
affinity for CB2 receptors is 13.8 nM, while its affinity for CB1 is 383 nM, meaning that it binds almost 28 times more strongly to CB2 than to CB1. However
JWH-015
Community District in New York, United States
the first members of what was then called a "Community Planning Board." CB2 was one of the first of these "Community Planning Boards." Susan Kent currently
Manhattan_Community_Board_2
Chemical compound
THC. O-1602 does not bind to the classical cannabinoid receptors CB1 or CB2 with any significant affinity, but instead is an agonist at several other
O-1602
— January 30, 2003 Anderson Mesa LONEOS THM 3.3 km MPC · JPL 172410 2003 CB2 — February 1, 2003 Anderson Mesa LONEOS EUP 8.4 km MPC · JPL 172411 2003
List of minor planets: 172001–173000
List_of_minor_planets:_172001–173000
Chemical compound
acts as a potent and selective inverse agonist for the cannabinoid receptor CB2. ADB-5'Br-PINACA AM-630 (6-Iodopravadoline) WIN 48,098 (Pravadoline) WIN
WIN_54,461
Protein-coding gene in the species Homo sapiens
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
LGR4
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
Thrombin_receptor
Chemical compound
cannabinoid receptor CB2, with a Ki of 0.28 nM at CB2 and 52.3 nM at the CB1 receptor, giving it around 180 times selectivity for CB2. The 2-methyl and 6-nitro
AM-1221
Chemical compound
is a potent selective CB2 receptor agonist with a Ki of 3.4nM and selectivity of around 200x for CB2 over CB1 receptors. It was discovered
JWH-133
American basketball player (born 2001)
the Missouri Sports Hall of Fame. Braun has launched a fashion line, The CB2 Collection. Corr, Joseph (June 6, 2023). "Christian Braun pronunciation,
Christian_Braun
Chemical compound
for the cannabinoid receptors, with a Ki of 13.5 nM at CB1 and 49.5 nM at CB2. AM-679 was one of the first 3-(2-iodobenzoyl)indole derivatives that was
AM-679_(cannabinoid)
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
Membrane_androgen_receptor
Chemical compound
potent CB1 agonist, with a binding affinity of 0.29nM for CB1 and 0.91nM for CB2, and an EC50 of 6.36 nM for CB1. ADB-BINACA ADB-PINACA ADB-HEXINACA ADB-5'F-BUTINACA
ADB-BUTINACA
Chemical compound
has Ki values of 1.14nM at CB1 and 0.1228nM at CB2 and EC50 values of 0.2668nM at CB1 and 0.1411nM at CB2. There have been a large number of reported cases
MDMB-FUBINACA
Type of drugs
Cannabinoid Receptor Agonists (SCRA) by binding to cannabinoid receptors CB1 and CB2 . Its binding towards CB1 receptor will lead to receptor phosphorylation
Synthetic_drug
Chemical compound
to be potent cannabinoid agonists with moderate to a high selectivity for CB2 over CB1. The first published synthesis and pharmacological evaluation of
AB-001
1998 Oizumi T. Kobayashi EOS 6.7 km (4.2 mi) MPC · JPL 8742 Bonazzoli 1998 CB2 Bonazzoli February 14, 1998 Colleverde V. S. Casulli slow 4.0 km (2.5 mi)
List of minor planets: 8001–9000
List_of_minor_planets:_8001–9000
Chemical compound
that acts as a potent and selective agonist for the cannabinoid receptor CB2, with reasonable selectivity over the psychoactive CB1 receptor, though with
MDA-19
Local government unit in New York City
members and/or staffers prior to becoming elected officials: Rafael Salamanca (CB2 member and District Manager) Eric Stevenson (politician) (CB3 member) Latoya
Community_boards_of_the_Bronx
Protein-coding gene in the species Homo sapiens
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
GPR37L1
Chemical compound
alongside MEPIRAPIM. FUBIMINA acts as a reasonably potent agonist for the CB2 receptor (Ki = 23.45 nM), with 12x selectivity over CB1 (Ki = 296.1 nM),
FUBIMINA
Protein-coding gene in the species Homo sapiens
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
LPAR5
UK biology research facility
of Cancer and Developmental Biology Address Tennis Court Road, Cambridge CB2 1QN Location Cambridge , Cambridgeshire, United Kingdom Website www.gurdon
Gurdon_Institute
Protein-coding gene in humans
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
GPR82
Protein-coding gene in the species Homo sapiens
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
GPRC5D
Chemical compound
which acts as a potent and selective cannabinoid CB2 receptor agonist, with 1400x selectivity for CB2 over the related CB1 receptor. Unlike most cannabinoid
CBS-0550
Chemical compound
chain. AMG-3 is a potent agonist at both CB1 and CB2 receptors with a Ki of 0.32 nM at CB1 and 0.52 nM at CB2, and its particularly high binding affinity has
AMG-3
Chemical compound
selective CB2 receptor agonist, with a Ki of 13.0 nM and selectivity of around 220 times for CB2 over CB1 receptors. It is related to other dibenzopyran CB2 agonists
JWH-359
Chemical compound
research. It has high affinity for both CB1 and CB2 receptors, with Ki values of 1.3 nM at CB1 and 0.57 nM at CB2, but is only moderately soluble in water compared
O-2372
Chemical compound
effects reported in rodent models may be mediated via CB2 receptors. 4-O-Methylhonokiol activates CB2 receptors and also inhibits the oxygenation of the
4-O-Methylhonokiol
Chemical compound
benzimidazole analog of JWH-018. It is presumed to be a potent agonist of the CB2 receptor and has been sold online as a designer drug. Related benzimidazole
BIM-018
hobby shops but are now often prized by collectors. CB1 Conan Unchained! CB2 Conan Against Darkness! RS1 Red Sonja Unconquered (Although not strictly
List of games based on Conan the Barbarian
List_of_games_based_on_Conan_the_Barbarian
Chemical compound
is a cannabinoid drug, which acts as a potent agonist at both the CB1 and CB2 receptors, but has poor blood–brain barrier penetration, and so produces
CB-13
THC precursor
exert immuno-modulating effect, not mediated by the cannabinoid CB1 and CB2 receptor coupled pathways like THC. THCA was able to inhibit the tumor necrosis
Tetrahydrocannabinolic_acid
Pharmaceutical compound
previously been targeted toward greater selectivity of the cannabinoid receptor CB2 over CB1. The activity of AB-MDMSBA against either cannabinoid receptor is
AB-MDMSBA
Kitami K. Endate, K. Watanabe · 4.8 km (3.0 mi) MPC · JPL 7436 Kuroiwa 1994 CB2 Kuroiwa February 8, 1994 Kitami K. Endate, K. Watanabe · 4.6 km (2.9 mi)
List of minor planets: 7001–8000
List_of_minor_planets:_7001–8000
Chemical compound
with Ki values of 0.9 nM at CB1 and 23.2 nM at CB2 and EC50 values of 1.8 nM at CB1 and 3.2 nM at CB2. It was originally developed by Pfizer in 2009 as
AB-FUBINACA
Psychoactive drug from the cannabis plant
found primarily in the brain as well as in some peripheral tissues, and the CB2 receptor is found primarily in peripheral tissues, but is also expressed
Cannabis_(drug)
Chemical compound
CB1 and 11.3 nM at CB2, suggesting a somewhat higher CB1 selectivity of 26 times, or alternatively 15.1 nM at CB1 and 34.8 nM at CB2 with only 2.3 times
5F-CUMYL-PINACA
Chemical compound
is illegal in the UK. WIN 55,212-2 is also a CB2 receptor agonist and thereby, like other cannabinoid CB2 agonists, found to significantly improve cardiac
WIN_55,212-2
Mathematics book by John Conway
Groups: Ten Years On. The Pitt Building, Trumpington Street, Cambridge, CB2 1RP: The Press Syndicate of the University of Cambridge. ISBN 978-0-521-57587-4
ATLAS_of_Finite_Groups
Australian furniture store chain owned by Greenlit Brands
stores around the country. In August 2017, Fantastic Furniture partnered with CB2 x Fred Segal. In 2016, it was included in the takeover of Furniture Holdings
Fantastic_Furniture
Chemical compound
potent cannabinoid agonist at both the CB1 and CB2 receptors, with Ki values of 0.46 nM at CB1 and 0.69 nM at CB2. It is one of the most potent 4-substituted
JWH-210
Chemical compound
and colleagues in 2007. It acts as a full agonist of the CB1 receptor and CB2 receptor with Ki values of 3 nM and 4 nM, respectively. Many related derivatives
QMPSB
Protein-coding gene in the species Homo sapiens
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
P2RY4
Protein family
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
Alpha-2_adrenergic_receptor
Group of protein families
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
Sex_hormone_receptor
University technical college in Cambridge, Cambridgeshire, England
Main academy building Location Robinson Way Cambridge , Cambridgeshire , CB2 0SZ England 52°10′29″N 0°08′25″E / 52.17479°N 0.14041°E / 52.17479; 0
Cambridge Academy for Science and Technology
Cambridge_Academy_for_Science_and_Technology
Chemical compound
a tricyclic aryl derivative that acts as a competitive antagonist at the CB2 cannabinoid receptor. Its activity at CB1 was significantly less effective
WIN_56,098
Chemical compound
morpholinylamide, is a drug used in scientific research that acts as a selective CB2 inverse agonist. BML-190 is structurally derived from the NSAID indomethacin
BML-190
Investigational antimigraine drugs
Δ9-tetrahydrocannabinol; Deltanyne; Elevat; Marinol) – cannabinoid CB1 and CB2 receptor agonist – migraine [83] Ergotamine inhalation (Tempo-ergotamine)
List of investigational headache and migraine drugs
List_of_investigational_headache_and_migraine_drugs
104th season in franchise history
Krys Barnes 13 1 1 ILB Quay Walker 17 CB Jaire Alexander Keisean Nixon 16 1 CB2 Eric Stokes Rasul Douglas 9 8 CB3 Rasul Douglas Keisean Nixon Darnell Savage
2022_Green_Bay_Packers_season
Cell surface protein binding somatostatin and triggering intracellular changes
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
Somatostatin_receptor
Chemical compound
and CB2 receptors. It is a potent and reasonably selective agonist for the CB1 cannabinoid receptor, with a Ki of 1.2 nM at CB1 and 5.3 nM at CB2. 1
AM-905
Protein-coding gene in the species Homo sapiens
2 EP 1 2 3 4 FP Prostacyclin Thromboxane Other Bile acid Cannabinoid CB1 CB2 GPR 18 55 119 EBI2 Estrogen Free fatty acid 1 2 3 4 Hydroxycarboxylic acids
GPRC5A
Pharmaceutical compound
partial agonist at CB1 receptors with a Ki of 5.6 nM, and an antagonist of CB2 receptors with a Ki of 7.9 nM. It has analgesic effects in studies on mice
CB-86
1760–1840 agrarian to industrial era shift
Douglas A. Galbi. Centre for History and Economics, King's College, Cambridge CB2 1ST. "Testimony Gathered by Ashley's Mines Commission". 2008. Archived from
Industrial_Revolution
Japanese amateur astronomer (born 1961)
11 December 1999 list (53549) 2000 BN14 28 January 2000 list (53553) 2000 CB2 2 February 2000 list (53633) 2000 DQ 24 February 2000 list (55813) 1994 VQ2
Takao_Kobayashi
CB2
CB2
CB2
CB2
Boy/Male
British, English
From the Sword Place
Boy/Male
Hindu
Pure, Eternally pure
Male
Hebrew
(יְש×ַעְיָה) Hebrew name YESHAYAH means "God is salvation." In the bible, this is the name of a great prophet called in English Isaiah.Â
Female
Danish
, of Magdala.
Surname or Lastname
English
English : occupational name for a scholar or schoolmaster, from an agent derivative of Middle English lern(en), which meant both ‘to learn’ and ‘to teach’ (Old English leornian).South German : habitational name for someone from Lern near Freising.South German : nickname from Middle High German lerner ‘pupil’, ‘schoolboy’.Jewish (Ashkenazic) : occupational name from Yiddish lerner ‘Talmudic student or scholar’.
Boy/Male
Indian
Son, Abhimanyu
Girl/Female
Indian, Traditional
Happiness
Girl/Female
Muslim/Islamic
Hidden Inner
Male
Welsh
Welsh form of Irish Goibniu, GOFANNON means "smith." In mythology, this is the name of a smith god, the son of Dôn.
Boy/Male
Arabic, Muslim
Servant of the Holy (Allah)
CB2
CB2
CB2
CB2
CB2