A-68930 hydrochloride structure
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Common Name | A-68930 hydrochloride | ||
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| CAS Number | 130465-39-3 | Molecular Weight | 307.77200 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C16H18ClNO3 | Melting Point | 250ºC | |
| MSDS | Chinese USA | Flash Point | N/A | |
Use of A-68930 hydrochlorideA68930 hydrochloride, as a dopamine D1 receptor agonist, can be used for the research of bronchiectasis[1]. |
| Name | A-68930 hydrochloride |
|---|---|
| Synonym | More Synonyms |
| Description | A68930 hydrochloride, as a dopamine D1 receptor agonist, can be used for the research of bronchiectasis[1]. |
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| Related Catalog | |
| Target |
D1 Receptor |
| In Vitro | A68930 hydrochloride (1 μM; 5-60 minutes; 16HBE14o- or NCI-H292 cells) significantly increases phosphorylation of cAMP response element binding (CREB) protein[1]. A68930 hydrochloride (1 μM; 48 hours; NCI-H292 cells) induces MUC5AC mRNA expression and increases the mRNA data of MUC5AC and MUC5AC protein expression[1]. A68930 hydrochloride (1 μM; 20 minutes; NCI-H292 cells) significantly increases intracellular cAMP levels[1]. Western Blot Analysis[1] Cell Line: 16HBE14o- or NCI-H292 cells Concentration: 1 μM Incubation Time: 5~60 minutes Result: Significantly increased phosphorylation of CREB. RT-PCR[1] Cell Line: NCI-H292 cells Concentration: 1 μM Incubation Time: 48 hours Result: Induced MUC5AC mRNA expression. Immunofluorescence[1] Cell Line: NCI-H292 cells Concentration: 1 μM Incubation Time: 48 hours Result: The mRNA data of MUC5AC, MUC5AC protein expression were increased. |
| References |
| Melting Point | 250ºC |
|---|---|
| Molecular Formula | C16H18ClNO3 |
| Molecular Weight | 307.77200 |
| Exact Mass | 307.09800 |
| PSA | 75.71000 |
| LogP | 3.91390 |
| InChIKey | PQPGUUQPTSMLKU-YYLIZZNMSA-N |
| SMILES | Cl.NCC1OC(c2ccccc2)Cc2c1ccc(O)c2O |
| Storage condition | -20°C |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| Safety Phrases | 22-24/25 |
| RIDADR | NONH for all modes of transport |
| HS Code | 2932999099 |
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A-68930 hydroch... CAS#:130465-39-3 |
| Literature: Journal of Medicinal Chemistry, , vol. 33, # 11 p. 2948 - 2950 |
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A-68930 hydroch... CAS#:130465-39-3 |
| Literature: Journal of Medicinal Chemistry, , vol. 33, # 11 p. 2948 - 2950 |
|
~%
A-68930 hydroch... CAS#:130465-39-3 |
| Literature: Journal of Medicinal Chemistry, , vol. 33, # 11 p. 2948 - 2950 |
|
~%
A-68930 hydroch... CAS#:130465-39-3 |
| Literature: Journal of Medicinal Chemistry, , vol. 33, # 11 p. 2948 - 2950 |
|
~%
A-68930 hydroch... CAS#:130465-39-3 |
| Literature: Journal of Medicinal Chemistry, , vol. 33, # 11 p. 2948 - 2950 |
|
~%
A-68930 hydroch... CAS#:130465-39-3 |
| Literature: Journal of Medicinal Chemistry, , vol. 33, # 11 p. 2948 - 2950 |
|
~%
A-68930 hydroch... CAS#:130465-39-3 |
| Literature: Journal of Medicinal Chemistry, , vol. 33, # 11 p. 2948 - 2950 |
|
~%
A-68930 hydroch... CAS#:130465-39-3 |
| Literature: Journal of Medicinal Chemistry, , vol. 33, # 11 p. 2948 - 2950 |
| HS Code | 2932999099 |
|---|---|
| Summary | 2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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A-68930, a novel, potent dopamine D1 receptor agonist: a microstructural analysis of its effects on feeding and other behaviour in the rat.
Behav. Pharmacol. 5 , 210-218 , (1994) A-68930 [1R, 3S)-1-aminomethyl-5,6-dihydroxy-3-phenylisochroman HCI] is a novel, potent and selective dopamine D1 receptor agonist. Previous reports have shown that the selective D1 partial agonist, S... |
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Sedative effects of the dopamine D1 receptor agonist A 68930 on rat open-field behavior.
Neuroreport 11 , 1269-1279, (2000) The present results demonstrate sedative effects of the DA D1 receptor agonist A 68930 (0.9-15 micromol kg(-1), s.c.) on rat spontaneous locomotor activity in an open field. The effects were particula... |
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A68930: a potent and specific agonist for the D-1 dopamine receptor.
Am. J. Hypertens. 3 , 40S-42S, (1990) A68930 (5,6-dihydroxy-3-phenyl-1-aminomethyl-isochroman) is a potent (EC50 = 2.5 nmol/L) partial agonist at the D-1 dopamine receptor. In contrast, A68930 is a much weaker agonist (EC50 = 3,920 nmol/L... |
| cis-1-(Aminomethyl)-3-phenylisochroman-5,6-diol hydrochloride |
| (1R,3S)-1-(aminomethyl)-3-phenyl-3,4-dihydro-1H-isochromene-5,6-diol,hydrochloride |