SCHEMBL161460

SCHEMBL161460

Cc1[nH]c2nc(CS(=O)(=O)O)nc(Nc3cccc(Cl)c3)c2c1C

nearest known ligand 0.58

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
EGFR P00533 13/20 0.58
ABL1 P00519 5/20 0.58
ABL2 P42684 5/20 0.58
MEN1 O00255 1/20 0.44
KMT2A Q03164 1/20 0.44
ALDH1A1 P00352 1/20 0.40
KDR P35968 1/20 0.39
PRKCA P17252 1/20 0.39
NPC1 O15118 1/20 0.39
HPGD P15428 1/20 0.39
HTT P42858 1/20 0.39
CSNK2A2 P19784 1/20 0.39
CSNK2B P67870 1/20 0.39
CSNK2A1 P68400 1/20 0.39
CSNK2A3 Q8NEV1 1/20 0.39

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
SCHEMBL8586040 0.83 EGFR (0.55) EGFRABL1ABL2PRKCANPC1
SCHEMBL2461575 0.81 EGFR (0.69) EGFRABL1ABL2MEN1KMT2A
SCHEMBL27627681 0.80 EGFR (0.91) EGFRABL1ABL2KDRPRKCA
SCHEMBL29795688 0.80 EGFR (0.91) EGFRABL1ABL2KDRPRKCA
SCHEMBL2463632 0.74 EGFR (1.00) EGFRABL1ABL2KDRPRKCA
SCHEMBL29406611 0.74 EGFR (1.00) EGFRABL1ABL2KDRPRKCA
SCHEMBL16964814 0.67 EGFR (0.40) EGFRABL1ABL2MEN1KMT2A
SCHEMBL7494877 0.65 EGFR (0.72) EGFRABL1ABL2PRKCA
SCHEMBL7491933 0.65 EGFR (0.72) EGFRABL1ABL2PRKCA
SCHEMBL7494688 0.65 EGFR (0.72) EGFRABL1ABL2PRKCA

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 94 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260132164-A1 PNU ANTHRACYCLINE DERIVATIVES AND METHODS OF USE THEREOF MERCK SHARP & DOHME LLC (US) 2026-05-14 US disclosed
EP-4076459-B1 PRMT5 INHIBITORS MERCK SHARP & DOHME LLC (US) 2026-04-29 EP disclosed
US-12595248-B2 PRMT5 inhibitors MERCK SHARP & DOHME LLC (US) 2026-04-07 US disclosed
US-12595262-B2 PRMT5 inhibitors MERCK SHARP & DOHME LLC (US) 2026-04-07 US disclosed
US-12583871-B2 PRMT5 inhibitors MERCK SHARP & DOHME LLC (US) 2026-03-24 US disclosed
US-12552826-B2 PRMT5 inhibitors MERCK SHARP & DOHME LLC (US) 2026-02-17 US disclosed
EP-4076460-B1 1,4-DIHYDRO-2H-SPIRO[ISOQUINOLINE-3,4'-PIPERIDINE DERIVATIVES AS PRMT5 INHIBITORS FOR THE TREATMENT OF CANCER MERCK SHARP & DOHME LLC (US) 2026-01-21 EP disclosed
US-12516321-B2 RNA interference mediated inhibition of gene expression using short interfering nucleic acids (siNA) SIRNA THERAPEUTICS, INC. (US) 2026-01-06 US disclosed
US-20260000691-A1 COMPOUNDS, METHODS, AND TREATMENTS FOR ABNORMAL SIGNALING PATHWAYS FOR PRENATAL AND POSTNATAL DEVELOPMENT JENNINGS BARBARA BROOKE (US) 2026-01-01 US disclosed
US-12486503-B2 Short interfering nucleic acid (siNA) compositions SIRNA THERAPEUTICS, INC. (US) 2025-12-02 US disclosed
US-8034815-B2 Imidazol-1-yl-(4-pyridin-2-yl-piperazin-1-yl)-methanethione; Critical Outcome Technologies' Iead compound (COTI); kinase inhibitor; anticarcinogenic agent; especially small cell lung cancer; cervical, ovarian, skin, prostate, breast, colorectal, head, neck, or kidney cancer, sarcoma, leukemia CRITICAL OUTCOME TECHNOLOGIES, INC. (CA) 2011-10-11 US disclosed
EP-2318406-A1 THIOSEMICARBAZONE INHIBITOR COMPOUNDS AND CANCER TREATMENT METHODS Critical Outcome Technologies, Inc. (CA) 2011-05-11 EP disclosed
WO-2011049722-A1 PYRAZOLO [3,4-b] PYRIDIN-4-ONE KINASE INHIBITORS MERCK SHARP & DOHME CORP. (US) 2011-04-28 WO disclosed
WO-2011022805-A1 NOVEL COLCHICINE DERIVATIVES, METHODS AND USES THEREOF ALBERTA HEALTH SERVICES (CA) 2011-03-03 WO disclosed
WO-2010006438-A1 THIOSEMICARBAZONE INHIBITOR COMPOUNDS AND CANCER TREATMENT METHODS CRITICAL OUTCOME TECHNOLOGIES INC. (CA) 2010-01-21 WO disclosed
US-20100015140-A1 Inhibitor Compounds and Cancer Treatment Methods CRITICAL OUTCOME TECHNOLOGIES INC. (CA) 2010-01-21 US disclosed
EP-2121681-A1 COMPOUNDS AND METHOD FOR TREATMENT OF CANCER Critical Outcome Technologies, Inc. (CA) 2009-11-25 EP disclosed
WO-2008083491-A1 COMPOUNDS AND METHOD FOR TREATMENT OF CANCER CRITICAL OUTCOME TECHNOLOGIES INC. (CA) 2008-07-17 WO disclosed
US-20080171744-A1 COMPOUNDS AND METHOD FOR TREATMENT OF CANCER 6441513 CANADA INC. (CA) 2008-07-17 US disclosed
WO-1998043973-A1 INTERMEDIATE PRODUCTS AND METHOD FOR THE PRODUCTION OF PYRIMIDINE DERIVATIVES NOVARTIS AG (CH) 1998-10-08 WO 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 (8 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-12595248-B2 PRMT5 inhibitors PRMT5, PRMT1, PRMT6 EGFR 3903/4885ABL1 651/4885ABL2 2085/4885
US-20260000691-A1 COMPOUNDS, METHODS, AND TREATMENTS FOR ABNORMAL SIGNALING PATHWAYS FOR PRENATAL AND POSTNATAL DEVELOPMENT PDK1, IP6K1, IP6K3 EGFR 3208/4885ABL1 4410/4885ABL2 4350/4885
US-20080171744-A1 COMPOUNDS AND METHOD FOR TREATMENT OF CANCER SLC6A6, SLCO1B3, SLC5A1 EGFR 1170/4885ABL1 1293/4885ABL2 3158/4885
US-20100015140-A1 Inhibitor Compounds and Cancer Treatment Methods MTOR, RICTOR, RPTOR EGFR 13/4885ABL1 484/4885ABL2 560/4885
US-12595262-B2 PRMT5 inhibitors PRMT1, PRMT5, CARM1 EGFR 2928/4885ABL1 326/4885ABL2 887/4885
US-20260132164-A1 PNU ANTHRACYCLINE DERIVATIVES AND METHODS OF USE THEREOF TOP1, NCL, NOLC1 EGFR 230/4885ABL1 146/4885ABL2 2251/4885
US-12583871-B2 PRMT5 inhibitors PRMT5, PRMT1, PRMT3 EGFR 4481/4885ABL1 455/4885ABL2 2353/4885
US-12552826-B2 PRMT5 inhibitors PRMT5, PRMT6, PRMT1 EGFR 2925/4885ABL1 503/4885ABL2 1999/4885

“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.