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Cat No. | Product Name | Synonyms | Targets |
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T16333 | NKY80 | Adenylyl cyclase type V Inhibitor | Adenylyl cyclase |
NKY80 regulates the adenylyl cyclase catalytic activity in heart and lung tissues. NKY80 is a non-competitive inhibitor of adenylyl cyclase type V isoform (IC50s: 8.3 µM, 132 µM, and 1.7 mM for type V, III and II, respe... | |||
T10066 | 2',5'-Dideoxyadenosine | Adenylyl cyclase , Adrenergic Receptor , AChR | |
2',5'-Dideoxyadenosine is a potent and non-competitive adenylyl cyclase inhibitor via binding the P-site (IC50: 3 μM). | |||
T15658 | KH7 | cAMP , AChR | |
KH7 is a soluble inhibitor of adenylyl cyclase (sAC)-specific. It has IC50s of 3-10 μM toward both recombinant purified human sACt protein and heterologously expressed sACt in cellular assays. KH7 is also a cAMP inhibito... | |||
T16938 | ST034307 | Adenylyl cyclase | |
ST034307 is an effective and selective inhibitor of adenylyl cyclase 1 (IC50: 2.3 μM). | |||
T60003 | AC1-IN-1 | Adenylyl cyclase | |
AC1-IN-1 is a selective inhibitor of adenylyl cyclase type 1 (AC1, IC50 = 0.54 µM). | |||
T0322 | Fipexide | Dopamine Receptor , AChR | |
Fipexide (Attentil, Vigilor), a psychoactive drug of the piperazine chemical class, was developed in Italy in 1983. It was served as a nootropic drug in France and Italy, mainly for the therapy of senile dementia, but is... | |||
T16275 | NB001 | HTS 09836 | Adenylyl cyclase |
NB001 (HTS 09836) is an inhibitor of adenyl cyclase 1 exhibiting effects on neural and non-neural pain. | |||
T83169 | Adenylyl cyclase-IN-1 | ||
Adenylyl cyclase-IN-1 is a potential adenylyl cyclase inhibitor for ocular hypotonia research [1]. | |||
T26869 | BMS-986122 | BMS 986122 | Opioid Receptor |
BMS-986122 (BMS 986122) is a positive allosteric modulator of μ-opioid receptors that increases β-arrestin recruitment stimulated by endomorphin 1 in U2OS-OPRM1 human osteosarcoma cells expressing μ-opioid receptors (EC5... | |||
T8702 | SKF-83566 | Dopamine Receptor , 5-HT Receptor , AChR | |
SKF-83566 is a blood-brain permeable and orally active antagonist of D1-like dopamine receptor and a weaker competitive 5-HT2 receptor antagonist with Ki of 11 nM | |||
T63893 | Adenylyl cyclase type 2 agonist-1 | ||
Adenylyl cyclase type 2 agonist-1 is a potent agonist of adenylyl cyclase type 2 (AC2) (EC50: 90 nM). It is a potential lead compound in the fight against respiratory diseases. | |||
T2172 | SQ22536 | 9-(tetrahydrofuran-2-yl)-9h-purin-6-amine,SQ 22536 | AChR |
SQ22536 (9-(tetrahydrofuran-2-yl)-9h-purin-6-amine) , the adenosine analogue 9-(Tetrahydro-2-furyl)adenine, inhibited adenylate cyclase activity of crude membrane preparations from catfish (Ictalurus melas) and rat isola... | |||
T11918 | Lysipressin | Lysine vasopressin,[Lys8]-Vasopressin | Others |
Lysipressin ([Lys8]-Vasopressin), Induces contraction of the rabbit urinary bladder smooth muscle, activate adenylate-cyclase. Lysipressin is Antidiuretic hormone that have been found in pigs and some marsupial families. | |||
T15787 | LRE1 | Adenylyl cyclase | |
LRE1 is a specific and allosteric soluble adenylyl cyclase inhibitor. | |||
T8959 | OS-3-106 | Dopamine Receptor | |
OS-3-106 is a novel arylamide phenylpiperazines, as partial agonists at the D3R in the adenylyl cyclase inhibition assay. | |||
T7813 | α-MSH | MSH, amide,CZEN-002,α-Melanocyte-Stimulating Hormone (MSH), amide | Melanocortin Receptor , Adenylyl cyclase |
α-MSH (MSH, amide) is amide stimulates melanocortin 1 receptor that results in the activation of adenylyl cyclase. | |||
T64355 | TDI-10229 | cAMP | |
TDI-10229 is a potent and orally available inhibitor of soluble adenylyl cyclase (sAC, ADCY10). TDI-10229 displays nanomolar inhibition of sAC in both biochemical and cellular assays (IC50= 195 nM). TDI-10229 exhibits mo... | |||
T22615 | BPIPP | Others | |
guanylyl cyclase (GC) and adenylyl cyclase (AC) inhibitor | |||
T26960 | CB7833407 | ||
CB7833407 is a selective Adenylyl Cyclase isoform-2 (AC2) inhibitor. | |||
T23863 | CB-6673567 | CB 6673567 | |
CB-6673567 is a selective inhibitor of adenylyl cyclase. | |||
T28622 | RU-0207148 | ||
RU-0207148 is a novel allosteric soluble adenylyl cyclase (sAC) inhibitor. | |||
T22467 | 1,9-Dideoxyforskolin | Others | |
The compound is an inactive analog of forskolin(an adenylyl cyclase activator). | |||
T69543 | CFM-1571(free base) | ||
CFM 1571 is the free base of CFM 1571 Hydrochloride (C291720), which acts as a soluble guanylyl cyclase (sGC) activator while ignoring adenylyl cyclase. | |||
T38782 | Mant-GTPγS | ||
Mant-GTPγS, an effective GTP analog, displays strong competitive inhibition of adenylyl cyclase (AC). Additionally, it acts as a potent inhibitor of YdeH. | |||
T83843 | 2'(3')-O-Anthraniloylguanosine-5'-O-triphosphate sodium | 2'(3')-ANT-GTP | |
2'(3')-O-Anthraniloylguanosine-5'-O-triphosphate (2'-ANT-GTP) and 3'-ANT-GTP are fluorescent derivatives of GTP that exhibit spontaneous isomerization. 2'(3')-ANT-GTP features an emission peak at 428 nm when excited at 3... | |||
T76657L | Human PTH-(1-31) amide | ||
Human PTH-(1-31) amide, an analog of PTH, effectively stimulates phosphatidylcholine hydrolysis and promotes the release of adenylyl cyclase [1]. | |||
T73297 | TDI-11861 | ||
TDI-11861, a second-generation soluble Adenylyl Cyclase (sAC, ADCY10) inhibitor, demonstrates slow dissociation rates and effectively inhibits sAC activity in cells, evidenced by an IC50 value of 5.5 nM. | |||
TP2033 | [Des-His1,Glu9]-Glucagon amide | des-His1-[Glu9]-Glucagon (1-29) amide | |
Glucagon receptor antagonist (pA2 = 7.2 for inhibition of glucagon-induced adenylyl cyclase activation in rat liver membranes); displays no agonist activity. Enhances glucose-stimulated pancreatic insulin release in vitr... | |||
T71122 | Carsatrin (free base) | ||
Carsatrin is purinylpiperazine derivative. as cardiotonic and antiarrhythmic. Carsatrin acts as positive inotropic agent that increases twitch tension and prolongs the action potential (AP) duration of ventricular muscle... | |||
T37131 | MS 15203 | ||
Potent and selective GPR171 partial agonist (EC50 = 90 nM; 28% inhibition of forskolin activated adenylyl cyclase activity in rat hypothalamic memebranes). Exhibits minimal binding to a panel of ~70 GPCRs and 10 other re... | |||
T70975 | Carsatrin succinate | ||
Carsatrin succinate is the salt form of Carsatin, a purinylpiperazine derivative used as a cardiotonic and antiarrhythmic. Carsatrin acts as positive inotropic agent that increases twitch tension and prolongs the action ... | |||
T36720 | Deacetylforskolin | ||
Deacetylforskolin is a diterpene and a derivative of forskolin that has been found inC. forskohliiand has diverse biological activities.1,2,3,4It activates rat adipocyte adenylyl cyclase (IC50= 20 μM) and inhibits glucos... | |||
T83820 | TNP-GTP sodium | TNP-Guanosine 5'-triphosphate | |
TNP-GTP, a fluorescent derivative of guanosine 5'-triphosphate (GTP), essential for protein synthesis and gluconeogenesis, exhibits an emission peak at 552 nm when excited at 410 nm in water. Its fluorescence intensity i... | |||
T83811 | 2'(3')-O-Anthraniloyladenosine-5'-O-triphosphate sodium | 2'(3')-ANT-ATP | |
2'(3')-O-Anthraniloyladenosine-5'-O-triphosphate (2'-ANT-ATP) and its isomer 3'-ANT-ATP are fluorescent derivatives of ATP that spontaneously isomerize. Emitting a maximum light of 428 nm when excited at 330 nm in water,... |
Cat No. | Product Name | Synonyms | Targets |
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T2939 | Forskolin | Coleonol,Colforsin | FXR , Adenylyl cyclase , AChR , Autophagy |
Forskolin (Coleonol) is a natural product, an adenylate cyclase activator (EC50=0.5 μM). Forskolin increases cAMP levels, activates PXR and FXR, and induces autophagy. Forskolin produces positive inotropic effects in the... |
Cat No. | Product Name | Species | Expression System |
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TMPH-00574 | Adenylate cyclase Protein, E. coli, Recombinant (His) | E. coli | in vitro E. coli expression system |
Catalyzes the formation of the second messenger cAMP from ATP. Its transcript is probably degraded by endoribonuclease LS (rnlA), decreasing cAMP levels and the negative regulator Crp-cAMP, which then induces its own tra... | |||
TMPH-00892 | A1AR Protein, Human, Recombinant (His) | Human | in vitro E. coli expression system |
Receptor for adenosine. The activity of this receptor is mediated by G proteins which inhibit adenylyl cyclase. | |||
TMPH-02672 | GIPR Protein, Mouse, Recombinant (His & Myc) | Mouse | E. coli |
This is a receptor for GIP. The activity of this receptor is mediated by G proteins which activate adenylyl cyclase. | |||
TMPH-01386 | GLP2R Protein, Human, Recombinant (His) | Human | HEK293 |
This is a receptor for glucagon-like peptide 2. The activity of this receptor is mediated by G proteins which activate adenylyl cyclase. | |||
TMPH-01378 | GIPR Protein, Human, Recombinant (His & Myc) | Human | HEK293 |
This is a receptor for GIP. The activity of this receptor is mediated by G proteins which activate adenylyl cyclase. | |||
TMPH-01377 | GIPR Protein, Human, Recombinant (His) | Human | E. coli |
This is a receptor for GIP. The activity of this receptor is mediated by G proteins which activate adenylyl cyclase. | |||
TMPH-01201 | DRD2 Protein, Human, Recombinant (His & Myc) | Human | E. coli |
Dopamine receptor whose activity is mediated by G proteins which inhibit adenylyl cyclase. Positively regulates postnatal regression of retinal hyaloid vessels via suppression of VEGFR2/KDR activity, downstream of OPN5. | |||
TMPH-01385 | GLP1R Protein, Human, Recombinant (His) | Human | HEK293 |
G-protein coupled receptor for glucagon-like peptide 1 (GLP-1). Ligand binding triggers activation of a signaling cascade that leads to the activation of adenylyl cyclase and increased intracellular cAMP levels. Plays a ... | |||
TMPH-01384 | GLP1R Protein, Human, Recombinant (E. coli, His) | Human | E. coli |
G-protein coupled receptor for glucagon-like peptide 1 (GLP-1). Ligand binding triggers activation of a signaling cascade that leads to the activation of adenylyl cyclase and increased intracellular cAMP levels. Plays a ... | |||
TMPH-03301 | GLP1R Protein, Rat, Recombinant (E. coli, His) | Rat | E. coli |
G-protein coupled receptor for glucagon-like peptide 1 (GLP-1). Ligand binding triggers activation of a signaling cascade that leads to the activation of adenylyl cyclase and increased intracellular cAMP levels. Plays a ... | |||
TMPH-02676 | GLP1R Protein, Mouse, Recombinant (His & SUMO) | Mouse | E. coli |
G-protein coupled receptor for glucagon-like peptide 1 (GLP-1). Ligand binding triggers activation of a signaling cascade that leads to the activation of adenylyl cyclase and increased intracellular cAMP levels. Plays a ... | |||
TMPY-03506 | VILIP1 Protein, Human, Recombinant | Human | E. coli |
VILIP-1, also known as VSNL1, is strongly expressed in granule cells of the cerebellum where it associates with membranes in a calcium-dependent manner and modulates intracellular signaling pathways of the central nervou... | |||
TMPY-02648 | PACAP receptor/ADCYAP1R1 Protein, Human, Recombinant (hFc) | Human | HEK293 |
Pituitary adenylate cyclase activating polypeptide (PACAP, Adcyap1) activation of PAC1 receptors ( Adcyap1r1) significantly increases excitability of guinea pig cardiac neurons. This modulation of excitability is mediate... | |||
TMPJ-01048 | VSNL1 Protein, Human, Recombinant (His) | Human | E. coli |
Visinin-Like Protein 1 (VILIP) is a a member of the Visinin/Recoverin subfamily of neuronal calcium sensor proteins. VILIP is strongly expressed in the Granule Cells of the Cerebellum where it associates with membranes i... | |||
TMPY-02236 | PTH1R Protein, Human, Recombinant (His) | Human | HEK293 |
Parathyroid hormone / parathyroid hormone-related peptide receptor, also known as PTH / PTHrP type I receptor, PTH/PTHr receptor, Parathyroid hormone 1 receptor, PTH1 receptor, PTH1R and PTHR, is a multi-pass membrane pr... |