9
4
3
3
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T16136 |
MRS-1706
|
Adenosine Receptor | GPCR/G Protein; Neuroscience |
MRS-1706 是一种选择性A2B 腺苷受体的反向激动剂,对人 A2B、A2A、A1和 A3受体的Ki 值分别为 1.39、112、157 和 230 nM。 | |||
T2334 |
Avanafil
阿伐那非,TA1790 |
PDE | Metabolism |
Avanafil (TA1790) 是一种高活性PDE-5抑制剂,IC50=5.2 nM,对PDE1,PDE6和PDE11活性较低。 | |||
T4546 |
Dinoprost tromethamine salt
Dinoprost Tromethamine,Zinoprost,Prostin F2 alpha,PGF2α THAM,Dinolytic,地诺前列素氨丁三醇,Prostaglandin F2α THAM |
Apoptosis; Endogenous Metabolite; Prostaglandin Receptor; Autophagy; PROTAC Linker | Apoptosis; Autophagy; GPCR/G Protein; Immunology/Inflammation; Metabolism; PROTAC |
Dinoprost tromethamine salt (PGF2α THAM) 是一种口服有效的前列腺素 F 受体激动剂。它是在子宫内膜腔上皮和黄体中局部产生的溶酶激素,在分娩过程中起关键作用。 | |||
T1398 |
Tadalafil
Cialis,他达那非,IC-351,西力士 |
Apoptosis; PDE | Apoptosis; Metabolism |
Tadalafil (IC-351) 是一种PDE5抑制剂,IC50为 1.8 nM。 | |||
T0096 |
Vardenafil
伐地那非,Vivanza,Levitra,Vardenafil hydrochloride |
PDE | Metabolism |
Vardenafil (Vivanza) 是选择性、高效的、具有口服活性的磷酸二酯酶5抑制剂,IC50=0.7 nM。它能够非竞争性地抑制环磷酸鸟苷水解,从而提高 cGMP 水平。它对 PDE1 (180 nM),PDE6 (11 nM),PDE2,PDE3,PDE4 (>1000 nM) 具有选择性。它可用于研究勃起功能障碍。 | |||
T35288 |
Z 300
Z-300,Z300 |
Others | Others |
Z 300 是一种组胺 H2 受体拮抗剂。 Z 300 抑制胃酸分泌并促进胃体区域的胃粘液代谢。 | |||
T24388 |
LASSBio-1359
LASSBio1359,LASSBio 1359 |
Others | Others |
LASSBio-1359 is an adenosine receptor agonist. It acts by inducing relaxation of the corpus cavernosum. It also acts as a novel selective phosphodiesterase. | |||
T26993 |
CGP 56999A
CGP56999A,CGP-56999A |
Others | Others |
CGP 56999A is an antagonist of GABA(B) receptor, it enhances expression of brain-derived neurotrophic factor and attenuates dopamine depletion in the rat corpus striatum. | |||
T37919 |
Prostaglandin F1α
PGF1α,Prostaglandin F1α |
Others | Others |
Prostaglandin F1α (PGF1α) is the putative metabolite of dihomo-γ-linolenic acid (DGLA) via the cyclooxygenase (COX) pathway. Both PGF1α and PGF2α have been shown to act as priming pheromones for male Atlantic salmon with a threshold concentration of 10-11 M. [1] PGF1α binds to the ovine corpus luteum FP receptor at only 8% of the relative potency of PGF2α. [2] It is only half as active as PGF2α in inducing human respiratory smooth muscle contractions in vitro. [3] |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T15133 |
Dinoprost
Prostaglandin F2a,PGF2α,地诺前列素 |
Endogenous Metabolite | Metabolism |
Dinoprost (Prostaglandin F2a) 是口服有效的、内源性的前列腺素 F 受体激动剂。它是在子宫内膜腔上皮和黄体中局部产生的溶酶激素。它在分娩过程中起关键作用。 | |||
T0478 |
Progesterone
孕酮,Pregn-4-ene-3,20-dione |
Estrogen/progestogen Receptor; Progesterone Receptor; Opioid Receptor; Endogenous Metabolite | Endocrinology/Hormones; GPCR/G Protein; Metabolism; Neuroscience; Others |
Progesterone (Pregn-4-ene-3,20-dione) 是类固醇激素,能够调节月经周期。 | |||
T6S2227 |
Spinosin
斯皮诺素,Flavoayamenin |
Others | Others |
Spinosin (Flavoayamenin) 是一种具有神经保护作用的 C-糖苷类黄酮,从 Zizyphus jujube 种子分离得到,能够激活 Nrf2/HO-1 通路,并抑制 Aβ1-42的产生和聚合。 | |||
TN4277 |
Isocupressic acid
|
cAMP; P450; PKA | GPCR/G Protein; Metabolism; Tyrosine Kinase/Adaptors |
Isocupressic acid induces abortion in pregnant cows when ingested primarily during the last trimester, it decrease affects the angiogenesis of the female reproductive system, the decrease in blood flow and apoptosis of corpus luteum-derived endothelial ce |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPJ-00577 |
INSL3 Protein, Human, Recombinant (His)
RLNL,Insulin-like 3,RLF,Leydig insulin-like peptide,INSL3,Re... |
Human | HEK293 Cells |
Insulin-like 3 is a protein that in humans is encoded by the INSL3 gene. It is a secreted protein that belongs to the insulin family. It is expressed in prenatal and postnatal Leydig cells and found as well in the corpus luteum, trophoblast, fetal membranes and breast. It may act as a hormone to regulate growth and differentiation of gubernaculum, and thus mediating intra-abdominal testicular descent.It is a ligand for LGR8 receptor. | |||
TMPY-03460 |
DCXR Protein, Human, Recombinant (His)
XR,P34H,HCR2,HCRII,PNTSU,SDR20C1,DCR,dicarbonyl/L-xylulose r... |
Human | E. coli |
DCXR, also known as HCR2, belongs to the short-chain dehydrogenases/reductases (SDR) family. It is highly expressed in kidney, liver and epididymis. In the epididymis, DCXR is mainly expressed in the proximal and distal sections of the corpus region. HCR2 is weakly or not expressed in brain, lung, heart, spleen and testis. DCXR catalyzes the NADPH-dependent reduction of several pentoses, tetroses, trioses, alpha-dicarbonyl compounds and L-xylulose. DCXR participates in the uronate cycle of... | |||
TMPY-01927 |
ANP32A Protein, Human, Recombinant (His & GST)
MAPM,PP32,I1PP2A,C15orf1,LANP,HPPCn,PHAPI,acidic (leucine-ri... |
Human | E. coli |
acidic leucine-rich nuclear phosphoprotein 32 family member A, also known as acidic nuclear phosphoprotein pp32, Leucine-rich acidic nuclear protein, Mapmodulin, Potent heat-stable protein phosphatase 2A inhibitor I1PP2A, Putative HLA-DR-associated protein I, PHAPI and ANP32A, is a nucleus, cytoplasm and endoplasmic reticulum. ANP32A / LANP is expressed in all tissues tested. It is highly expressed in kidney and skeletal muscle, moderate levels of expression is in brain, placenta and panc... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMID-0037 |
Tadalafil-d3
|
||
Tadalafil-d3 是 Tadalafil 的氘代化合物。Tadalafil 的 CAS 号为 171596-29-5。Tadalafil 是一种PDE5抑制剂,IC50为 1.8 nM。 | |||
TMID-0209 |
Tadalafil-13C-d3
|
||
Tadalafil-13C-d3 是 Tadalafil 的 13C 和氘代化合物。Tadalafil 的 CAS 号为 171596-29-5。Tadalafil 是一种PDE5抑制剂,IC50为 1.8 nM。 | |||
TMIJ-0114 |
Vardenafil-d5
|
||
Vardenafil-d5 是 Vardenafil 的氘代化合物。Vardenafil 的 CAS 号为 224785-90-4。Vardenafil 是选择性、高效的、具有口服活性的磷酸二酯酶5抑制剂,IC50=0.7 nM。它能够非竞争性地抑制环磷酸鸟苷水解,从而提高 cGMP 水平。它对 PDE1 (180 nM),PDE6 (11 nM),PDE2,PDE3,PDE4 (>1000 nM) 具有选择性。它可用于研究勃起功能障碍。 |