General Information of the Compound
Compound ID
CP0080849
Compound Name
10-[3-(hydroxymethyl)-4-[1-methyl-5-[[5-[(2S)-2-methyl-4-(oxetan-3-yl)piperazin-1-yl]pyridin-2-yl]amino]-6-oxopyridin-3-yl]pyridin-2-yl]-4,4-dimethyl-1,10-diazatricyclo[6.4.0.02,6]dodeca-2(6),7-dien-9-one
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Synonyms
Fenebrutinib
GDC-0853
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Structure
Formula
C37H44N8O4
Molecular Weight
664.811
Canonical SMILES
C[C@H]1CN(CCN1c1ccc(Nc2cc(cn(C)c2=O)-c2ccnc(N3CCn4c5CC(C)(C)Cc5cc4C3=O)c2CO)nc1)C1COC1
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InChI
InChI=1S/C37H44N8O4/c1-23-18-42(27-21-49-22-27)9-10-43(23)26-5-6-33(39-17-26)40-30-13-25(19-41(4)35(30)47)28-7-8-38-34(29(28)20-46)45-12-11-44-31(36(45)48)14-24-15-37(2,3)16-32(24)44/h5-8,13-14,17,19,23,27,46H,9-12,15-16,18,20-22H2,1-4H3,(H,39,40)/t23-/m0/s1
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InChIKey
WNEODWDFDXWOLU-QHCPKHFHSA-N
CAS
1434048-34-6
Physicochemical Property
logP
3.5742
Rotatable Bonds
7
Heavy Atom Count
49
Polar Areas
120.99
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
11
Complexity
49

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

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PubChem ID
CID: 86567195
ChEMBL ID
CHEMBL4065122
DrugBank ID
DB14785
Clinical Information about the Compound
Drug 1 ( GDC-0853 )
Drug Name GDC-0853
Company GenentechSouth San Francisco, CA
Indication
Multiple sclerosis
Phase 3
Chronic idiopathic urticaria
Phase 2
Solid tumour/cancer
Phase 1
Autoimmune disease
Phase 1
Target(s)
Tyrosine-protein kinase BTK (ATK)
Inhibitor