Ki Summary

Reaction Details

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Target

5-hydroxytryptamine receptor 2A

Ligand

BDBM106529

Substrate/Competitor

n/a

Meas. Tech.

Radioligand Binding Assay

4.51±0.0 nM

Citation

Gobbi, L; Rodriguez Sarmiento, RM; Wichmann, J Anellated pyridine compounds US Patent US8586579 Publication Date 11/19/2013

More Info.:

Get all data from this article, Assay Method

5-hydroxytryptamine receptor 2A

Name:

5-hydroxytryptamine receptor 2A

Synonyms:

Type:

undefined

Mol. Mass.:

52607.65

Organism:

Homo sapiens (Human)

Description:

P28223

Residue:

471

Sequence:

MDILCEENTSLSSTTNSLMQLNDDTRLYSNDFNSGEANTSDAFNWTVDSENRTNLSCEGC
LSPSCLSLLHLQEKNWSALLTAVVIILTIAGNILVIMAVSLEKKLQNATNYFLMSLAIAD
MLLGFLVMPVSMLTILYGYRWPLPSKLCAVWIYLDVLFSTASIMHLCAISLDRYVAIQNP
IHHSRFNSRTKAFLKIIAVWTISVGISMPIPVFGLQDDSKVFKEGSCLLADDNFVLIGSF
VSFFIPLTIMVITYFLTIKSLQKEATLCVSDLGTRAKLASFSFLPQSSLSSEKLFQRSIH
REPGSYTGRRTMQSISNEQKACKVLGIVFFLFVVMWCPFFITNIMAVICKESCNEDVIGA
LLNVFVWIGYLSSAVNPLVYTLFNKTYRSAFSRYIQCQYKENKKPLQLILVNTIPALAYK
SSQLQMGQKKNSKQDAKTTDNDCSMVALGKQHSEEASKDNSDGVNEKVSCV

BDBM106529

n/a

Name

BDBM106529

Synonyms:

US8586579, 118

Type

Small organic molecule

Emp. Form.

C31H44N6O2

Mol. Mass.

532.7201

SMILES

CN1CCN(CC1)c1ccc(cc1)C(=O)N[C@H]1CC[C@H](CCN2CCN(CC2)c2nccc3OCCc23)CC1 |r,wU:16.17,wD:19.21,(13.77,.52,;12.23,.52,;11.46,-.82,;9.92,-.82,;9.15,.52,;9.92,1.85,;11.46,1.85,;7.8,.52,;7.03,-.82,;5.49,-.82,;4.72,.52,;5.49,1.85,;7.03,1.85,;3.18,.52,;2.41,-.82,;2.41,1.85,;.87,1.85,;.1,.52,;-1.44,.52,;-2.21,1.85,;-3.75,1.85,;-4.52,.52,;-6.06,.52,;-6.83,-.82,;-8.37,-.82,;-9.15,.52,;-8.37,1.85,;-6.83,1.85,;-10.69,.52,;-11.46,1.85,;-13,1.85,;-13.77,.52,;-13,-.82,;-13.48,-2.28,;-12.23,-3.19,;-10.99,-2.28,;-11.46,-.82,;-1.44,3.19,;.1,3.19,)|

Structure