Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T16563 | Pozanicline
化合物 T16563
|
161417-03-4 | 98% |
|
Pozanicline reverses nicotine withdrawal-induced cognitive deficits, may be an effective component of novel therapeutic strategies for nicotine addiction. Pozani... | ||||
TN1790 | Isopteropodine
钩藤碱 E
|
5171-37-9 | 98% |
|
Isopteropodine (Uncarine E) 是从 Hamelia patens micropropagated 分离得到的一种异育亨宾型辛吲哚生物碱.具有抗菌活性,可刺激机体免疫系统。Isopteropodine 是 M1 型毒蕈碱乙酰胆碱 (muscarinic M1) 受体及 5-HT2 受体的正向调节剂... | ||||
TN3875 | Dipterocarpol
化合物 TN3875
|
471-69-2 | 98% |
|
Dipterocarpol is a dammarane-type triterpenoid, as are the major bioactive compounds of ginseng. Dipterocarpol A shows moderate acetylcholinesterase inhibitory a... | ||||
TN2067 | Picfeltarraegenin X
苦玄参苷X
|
1391826-61-1 | 98% |
|
Picfeltarraenin X shows stronger AChE inhibition than the known AChE inhibitor Tacrine. | ||||
T12525 | Pozanicline dihydrochloride
化合物Pozanicline dihydrochloride
|
161416-61-1 | 98% |
|
Pozanicline dihydrochloride (ABT-089 dihydrochloride) 是口服有效的烟碱型乙酰胆碱受体激动剂,与 [3H] 胱氨酸位点结合,Ki 为 16.7 nM,对 α4β2 nAChR 的选择性高于α7nAChR。 | ||||
T12191 | NBTGR
化合物 T12191
|
13153-27-0 | 98% |
|
NBTGR is a potent nucleoside transport inhibitor(adenosine uptake ,Ki of 70 nM). | ||||
T19623 | α-Muricholic acid
化合物 T19623
|
2393-58-0 | 98% |
|
α-Muricholic acid is the most abundant primary bile acid in rodents. | ||||
TN2504 | 1,5-Dihydroxyxanthone
化合物 TN2504
|
14686-65-8 | 98% |
|
1,5-Dihydroxyxanthone exhibits the epidermal growth factor receptor (EGFR) -tyrosine kinase inhibitory activity, with the IC50 value of 90.34 nM. It may have ant... | ||||
TN4812 | Pluviatolide
化合物 TN4812
|
28115-68-6 | 98% |
|
(-)-Pluviatolide can inhibit electrically-induced and acetylcholine-induced contraction in the isolated guinea-pig ileum. | ||||
T16417 | Oxitropium Bromide
氧托溴铵
|
30286-75-0 | 98% |
|
Oxitropium bromide is a mAChR antagonist. It is used as an anticholinergic bronchodilator drug for the treatment of asthma and chronic obstructive pulmonary dise... | ||||
T13256 | UP202-56
化合物 T13256
|
163838-04-8 | 98% |
|
UP202-56 is an adenosinergic agonist and is an adenosine analog. | ||||
TN4456 | Lucidadiol
化合物 TN4456
|
252351-95-4 | 98% |
|
Lucidadiol exhibits butyrylcholinesterase-inhibitory activity at concentrations up to 200 uM, it also possesses inhibitory activity against acetylcholinesterase ... | ||||
T12868 | Sch412348
化合物 T12868
|
377727-26-9 | 98% |
|
Sch412348 is a potent competitive the human adenosine A2A receptor antagonist with Ki of 0.6 nM and has >1000-fold selectivity over all other adenosine receptors... | ||||
TN1409 | Asimilobine
巴婆碱
|
6871-21-2 | 98% |
|
(-)-Asimilobine shows antioxidative, anti-acetylcholinesterase (AChE), anti-α±-glucosidase, anti-leishmanial and anti-fungal activities; it displays weak inhibit... | ||||
T10731 | CDD0102
化合物 T10731
|
146422-58-4 | 98% |
|
CDD0102 is a potent agonist of M1 Muscarinic receptor. | ||||
T12446 | Phenserine
化合物 T12446
|
101246-66-6 | 98% |
|
Phenserine is a derivative of Physostigmine and is annoncompetitive, long-acting and selective inhibitor of AChE. | ||||
T5476 | MAChr-in-1
化合物mAChr-in-1
|
119391-56-9 | 98% |
|
mAChR-IN-1 是一种毒蕈碱胆碱能受体拮抗剂,IC50为17 nM。 | ||||
T13772 | MHP 133
化合物 T13772
|
147340-43-0 | 98% |
|
MHP 133 is a drug with multiple CNS targets(AChE with Ki of 69 μM). | ||||
T8868 | 4BP-TQS
化合物4BP-TQS
|
360791-49-7 | 99.99% |
|
4BP-TQS 是 α7nAChR 变构激动剂。它利用变构跨膜位点激活 nAChRs。 | ||||
T8552 | PSEM 89S TFA
化合物PSEM 89S TFA
|
1336913-03-1 | 99.98% |
|
PSEM 89S TFA 是一种脑渗透性和选择性离子通道激动剂,分别对 Q79G 和 L141F 具有正交选择性。 |