SCHEMBL6435573

SCHEMBL6435573

CC(C)(C)OC(=O)N1CCC(n2nc(-c3ccc(Oc4ccccc4)cc3)c3c(N)ncnc32)C1

nearest known ligand 0.74

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BTK Q06187 20/20 0.74
FLT3 P36888 2/20 0.69
KIT P10721 1/20 0.69
EGFR P00533 5/20 0.69
ITK Q08881 3/20 0.68
LCK P06239 2/20 0.68
TEC P42680 3/20 0.67
BMX P51813 3/20 0.67
TXK P42681 2/20 0.67
LYN P07948 2/20 0.67
FGFR2 P21802 2/20 0.67
RIPK2 O43353 1/20 0.67
NR1I2 O75469 1/20 0.67
SLC22A3 O75751 1/20 0.67
LATS1 O95835 1/20 0.67
NUDT14 O95848 1/20 0.67
ABL1 P00519 1/20 0.67
ERBB2 P04626 1/20 0.67
FYN P06241 1/20 0.67
PGR P06401 1/20 0.67

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL18123564 1.00 BTK (0.74) BTKFLT3KITEGFRITK
SCHEMBL30718180 0.95 BTK (0.68) BTKFLT3KITEGFRITK
SCHEMBL22720965 0.95 BTK (0.68) BTKFLT3KITEGFRITK
SCHEMBL15641034 0.95 BTK (0.81) BTKFLT3KITEGFRITK
SCHEMBL1628863 0.95 BTK (0.81) BTKFLT3KITEGFRITK
SCHEMBL30324920 0.95 BTK (0.81) BTKFLT3KITEGFRITK
SCHEMBL29671300 0.95 BTK (0.81) BTKFLT3KITEGFRITK
SCHEMBL12808088 0.95 BTK (0.81) BTKFLT3KITEGFRITK
SCHEMBL17951556 0.95 BTK (0.73) BTKFLT3KITEGFRITK
SCHEMBL19230406 0.94 BTK (0.77) BTKFLT3KITEGFRITK

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118027041-A BTK inhibitor ring derivative and preparation method and pharmaceutical application thereof 西藏海思科制药有限公司 2024-05-14 CN disclosed
CN-113544130-B BTK inhibitor ring derivative and preparation method and pharmaceutical application thereof 西藏海思科制药有限公司 2024-01-09 CN disclosed
US-11542266-B1 Substituted piperidines as BTK inhibitors HAISCO PHARMACEUTICALS PTE. LTD. (SG) 2023-01-03 US disclosed
US-11542266-B1 Substituted piperidines as BTK inhibitors HAISCO PHARMACEUTICALS PTE. LTD. (SG) 2023-01-03 US disclosed
EP-3978496-A1 BTK INHIBITOR RING DERIVATIVE, PREPARATION METHOD THEREFOR AND PHARMACEUTICAL APPLICATION THEREOF Haisco Pharmaceuticals Pte. Ltd. (SG) 2022-04-06 EP disclosed
CN-113544130-A BTK inhibitor ring derivative, preparation method and pharmaceutical application thereof 四川海思科制药有限公司 2021-10-22 CN disclosed
WO-2020239103-A1 BTK INHIBITOR RING DERIVATIVE, PREPARATION METHOD THEREFOR AND PHARMACEUTICAL APPLICATION THEREOF 四川海思科制药有限公司 2020-12-03 WO disclosed
WO-2020239103-A1 BTK INHIBITOR RING DERIVATIVE, PREPARATION METHOD THEREFOR AND PHARMACEUTICAL APPLICATION THEREOF 四川海思科制药有限公司 2020-12-03 WO disclosed
US-20170281810-A1 PHARMACEUTICAL COMPOSITIONS AND THEIR USE FOR TREATMENT OF CANCER AND AUTOIMMUNE DISEASES Zhejiang DTRM Biopharma Co. Ltd. (CN) 2017-10-05 US disclosed
US-9717745-B2 Pharmaceutical compositions and their use for treatment of cancer and autoimmune diseases Zhejiang DTRM Biopharma Co. Ltd. (CN) 2017-08-01 US disclosed
US-20160324878-A1 PHARMACEUTICAL COMPOSITIONS AND THEIR USE FOR TREATMENT OF CANCER AND AUTOIMMUNE DISEASES Zhejiang DTRM Biopharma Co. Ltd. (CN) 2016-11-10 US disclosed
US-7741330-B1 Pyrazolo-pyrimidine inhibitors of Bruton's tyrosine kinase PHARMACYCLICS, INC. (US) 2010-06-22 US disclosed
US-7741330-B1 Pyrazolo-pyrimidine inhibitors of Bruton's tyrosine kinase PHARMACYCLICS, INC. (US) 2010-06-22 US disclosed
US-6921763-B2 Pyrazolopyrimidines as therapeutic agents ABBOTT LABORATORIES (US) 2005-07-26 US disclosed
US-6660744-B1 Kinase inhibitors ABBOTT GMBH & CO. KG (DE) 2003-12-09 US disclosed
EP-1212327-B1 PYRAZOLOPYRIMIDINES AS THERAPEUTIC AGENTS BASF AG (DE) 2003-08-20 EP disclosed
US-20020156081-A1 Pyrazolopyrimidines as therapeutic agents ABBOTT LABORATORIES (US) 2002-10-24 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-11542266-B1 Substituted piperidines as BTK inhibitors BTK, BLK, SYK BTK 1/4885FLT3 83/4885KIT 801/4885
US-20170281810-A1 PHARMACEUTICAL COMPOSITIONS AND THEIR USE FOR TREATMENT OF CANCER AND AUTOIMMUNE DISEASES BTK, BCL9, BCL9L BTK 1/4885FLT3 302/4885KIT 1270/4885
US-20160324878-A1 PHARMACEUTICAL COMPOSITIONS AND THEIR USE FOR TREATMENT OF CANCER AND AUTOIMMUNE DISEASES BTK, BCL9, BCL9L BTK 1/4885FLT3 302/4885KIT 1270/4885
US-20020156081-A1 Pyrazolopyrimidines as therapeutic agents DPYD, CYP2D6, UGT1A1 BTK 1020/4885FLT3 67/4885KIT 445/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.