Ki Summary

Reaction Details

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Target

Apoptosis regulator Bcl-2

Ligand

BDBM189477

Substrate/Competitor

n/a

Meas. Tech.

Time Resolved-Fluorescence Resonance Energy Transfer (TR-FRET) Assay

Temperature

298.15±n/a K

0.01±n/a nM

Comments

extracted

Citation

Bruncko, M; Ding, H; Doherty, GA; Elmore, SW; Hasvold, LA; Hexamer, L; Kunzer, AR; Song, X; Souers, AJ; Sullivan, GM; Tao, Z; Wang, GT; Wang, L; Wang, X; Wendt, MD; Mantei, RA; Hansen, TM Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases US Patent US9174982 Publication Date 11/3/2015

More Info.:

Get all data from this article, Assay Method

Apoptosis regulator Bcl-2

Name:

Apoptosis regulator Bcl-2

Synonyms:

Type:

Homodimer or heterodimer

Mol. Mass.:

26269.11

Organism:

Homo sapiens (Human)

Description:

P10415

Residue:

239

Sequence:

MAHAGRTGYDNREIVMKYIHYKLSQRGYEWDAGDVGAAPPGAAPAPGIFSSQPGHTPHPA
ASRDPVARTSPLQTPAAPGAAAGPALSPVPPVVHLTLRQAGDDFSRRYRRDFAEMSSQLH
LTPFTARGRFATVVEELFRDGVNWGRIVAFFEFGGVMCVESVNREMSPLVDNIALWMTEY
LNRHLHTWIQDNGGWDAFVELYGPSMRPLFDFSWLSLKTLLSLALVGACITLGAYLGHK

BDBM189477

n/a

Name

BDBM189477

Synonyms:

US9174982, 29 | US9174982, 34

Type

Small organic molecule

Emp. Form.

C47H54ClN7O7S

Mol. Mass.

896.492

SMILES

COC1CCC(CNc2ccc(cc2[N+]([O-])=O)S(=O)(=O)NC(=O)c2ccc(cc2Oc2cnc3[nH]ccc3c2)N2CCN(CC3=C(CC(C)(C)CC3)c3ccc(Cl)cc3)CC2)CC1 |t:48,(-11.38,3.51,;-10.61,2.18,;-9.07,2.18,;-8.3,.84,;-6.76,.84,;-5.99,2.18,;-4.45,2.18,;-3.68,3.51,;-2.14,3.51,;-1.37,2.18,;.17,2.18,;.94,3.51,;.17,4.84,;-1.37,4.84,;-2.14,6.18,;-1.37,7.51,;-3.68,6.18,;2.48,3.51,;2.48,5.05,;4.02,3.51,;2.48,1.97,;3.81,1.2,;5.15,1.97,;3.81,-.34,;5.15,-1.11,;5.15,-2.65,;3.81,-3.42,;2.48,-2.65,;2.48,-1.11,;1.15,-.34,;-.19,-1.11,;-.19,-2.65,;-1.52,-3.42,;-2.85,-2.65,;-4.32,-3.12,;-5.22,-1.88,;-4.32,-.63,;-2.85,-1.11,;-1.52,-.34,;3.81,-4.96,;5.15,-5.73,;5.15,-7.27,;3.81,-8.04,;3.81,-9.58,;5.15,-10.35,;5.15,-11.89,;6.48,-12.66,;7.81,-11.89,;8.63,-13.19,;9.35,-11.94,;7.81,-10.35,;6.48,-9.58,;3.81,-12.66,;3.81,-14.2,;2.48,-14.97,;1.15,-14.2,;-.19,-14.97,;1.15,-12.66,;2.48,-11.89,;2.48,-7.27,;2.48,-5.73,;-6.76,3.51,;-8.3,3.51,)|

Structure