SCHEMBL2015374

SCHEMBL2015374

Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(Br)cc23)c1F

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BRAF P15056 6/20 0.66
CYP2C19 P33261 8/20 0.48
CYP2C9 P11712 5/20 0.48
RIPK2 O43353 2/20 0.48
RAF1 P04049 2/20 0.48
KDR P35968 2/20 0.48
MAP2K2 P36507 2/20 0.48
TGFBR2 P37173 2/20 0.48
NEK2 P51955 2/20 0.48
MAP2K1 Q02750 2/20 0.48
TNK2 Q07912 2/20 0.48
MAP2K5 Q13163 2/20 0.48
PTK6 Q13882 2/20 0.48
NEK11 Q8NG66 2/20 0.48
MAP3K20 Q9NYL2 2/20 0.48
MAP4K5 Q9Y4K4 2/20 0.48
BMPR1B O00238 1/20 0.48
PLK4 O00444 1/20 0.48
PIR O00625 1/20 0.48
AURKA O14965 1/20 0.48

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
SCHEMBL29482811 1.00 BRAF (0.66) BRAFCYP2C19CYP2C9RIPK2RAF1
SCHEMBL3702167 0.89 BRAF (0.58) BRAFCYP2C19CYP2C9RIPK2RAF1
SCHEMBL30313440 0.89 BRAF (0.58) BRAFCYP2C19CYP2C9RIPK2RAF1
SCHEMBL15677286 0.89 BRAF (0.53) BRAFCYP2C19CYP2C9RIPK2RAF1
SCHEMBL3704338 0.89 BRAF (0.53) BRAFCYP2C19CYP2C9RIPK2RAF1
SCHEMBL25447211 0.89 BRAF (0.58) BRAFCYP2C19CYP2C9RIPK2RAF1
SCHEMBL13505690 0.88 BRAF (0.52) BRAFCYP2C19CYP2C9RIPK2RAF1
SCHEMBL3505940 0.88 CYP2C19 (0.52) BRAFCYP2C19CYP2C9RIPK2RAF1
SCHEMBL2354890 0.88 BRAF (0.64) BRAFCYP2C19CYP2C9RIPK2RAF1
SCHEMBL3703309 0.87 BRAF (0.51) BRAFCYP2C19CYP2C9RIPK2RAF1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1893612-B1 PYRROLO [2, 3-B]PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS PLEXXIKON INC (US) 2011-08-03 EP claimed
US-20260115296-A1 COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF RAPIDLY ACCELERATED FIBROSARCOMA POLYPEPTIDES UNIV YALE (US) 2026-04-30 US disclosed
US-12559492-B2 BRAF degraders C4 THERAPEUTICS, INC. (US) 2026-02-24 US disclosed
US-20250236612-A1 RAPIDLY ACCELERATING FIBROSARCOMA PROTEIN DEGRADING COMPOUNDS AND ASSOCIATED METHODS OF USE ARVINAS OPERATIONS, INC. 2025-07-24 US disclosed
US-20250195516-A1 COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR PLEXXIKON INC (US) 2025-06-19 US disclosed
US-12180193-B2 Accelerating fibrosarcoma protein degrading compounds and associated methods of use ARVINAS OPERATIONS, INC. (US) 2024-12-31 US disclosed
EP-3700574-B1 FORMULATIONS OF A COMPOUND MODULATING KINASES PLEXXIKON INC (US) 2024-08-28 EP disclosed
US-11986531-B2 Compounds and methods for the targeted degradation of rapidly accelerated fibrosarcoma polypeptides ARVINAS OPERATIONS, INC. (US) 2024-05-21 US disclosed
US-11912701-B2 Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death HEPAREGENIX GMBH (DE) 2024-02-27 US disclosed
US-11912701-B2 Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death HEPAREGENIX GMBH (DE) 2024-02-27 US disclosed
WO-2010129567-A1 PYRROLO [2, 3. B] PYRIDINES WHICH INHIBIT RAF PROTEIN KINASE PLEXXIKON, INC. (US) 2010-11-11 WO disclosed
WO-2010129570-A1 SOLID FORMS OF SULFONAMIDES AND AMINO ACIDS PLEXXIKON, INC. (US) 2010-11-11 WO disclosed
US-20100286142-A1 Compounds and Methods for Kinase Modulation, and Indications Therefor PLEXXIKON, INC. 2010-11-11 US disclosed
US-20100286178-A1 COMPOUNDS AND USES THEREOF PLEXXIKON INC. 2010-11-11 US disclosed
US-20100256365-A1 COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR PLEXXIKON, INC. 2010-10-07 US disclosed
US-20100249118-A1 protein kinase modulators such as Propane-1-sulfonic acid [2,4-difluoro-3-(5-ethoxy-1H-pyrrolo[1,3-b]pyridine-3-carbonyl)-phenyl]-amide, used to regulate signal transduction cascades, involved in the control of physiological functions including cellular growth and proliferation; anticarcinogenic agents PLEXXIKON INC. 2010-09-30 US disclosed
WO-2010104945-A1 PYRROLO [2, 3-B] PYRIDINE DERIVATIVES FOR THE INHIBITION OF RAF KINASES PLEXXIKON, INC. (US) 2010-09-16 WO disclosed
EP-1893612-A1 PYRROLO [2, 3-B]PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS PLEXXIKON, INC. (US) 2008-03-05 EP disclosed
WO-2007002325-A1 PYRROLO[2,3-B] PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS PLEXXIKON, INC. (US) 2007-01-04 WO disclosed
WO-2007002433-A1 PYRROLO [2, 3-B] PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS PLEXXIKON, INC. (US) 2007-01-04 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 (11 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-20100249118-A1 protein kinase modulators such as Propane-1-sulfonic acid [2,4-difluoro-3-(5-ethoxy-1H-pyrrolo[1,3-b]pyridine-3-carbonyl)-phenyl]-amide, used to regulate signal transduction cascades, involved in the control of physiological functions including cellular growth and proliferation; anticarcinogenic agents MAP4K1, MAP4K2, MAP3K1 BRAF 95/4885CYP2C19 4868/4885CYP2C9 4869/4885
US-11912701-B2 Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death MAPK4, MAPK7, MAPK14 BRAF 64/4885CYP2C19 2763/4885CYP2C9 1742/4885
US-12559492-B2 BRAF degraders BRAF, NRAS, HRAS BRAF 1/4885CYP2C19 3525/4885CYP2C9 2913/4885
US-12180193-B2 Accelerating fibrosarcoma protein degrading compounds and associated methods of use CRBN, RBX1, ARAF BRAF 6/4885CYP2C19 4762/4885CYP2C9 4679/4885
US-20250236612-A1 RAPIDLY ACCELERATING FIBROSARCOMA PROTEIN DEGRADING COMPOUNDS AND ASSOCIATED METHODS OF USE CRBN, RBX1, ARAF BRAF 4/4885CYP2C19 4774/4885CYP2C9 4691/4885
US-20100286142-A1 Compounds and Methods for Kinase Modulation, and Indications Therefor BRAF, ARAF, RAF1 BRAF 1/4885CYP2C19 2678/4885CYP2C9 2237/4885
US-20100256365-A1 COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR MAP3K20, MAP3K13, MAP3K8 BRAF 48/4885CYP2C19 4579/4885CYP2C9 4746/4885
US-20250195516-A1 COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR MAP3K20, PRKACA, MAP3K13 BRAF 49/4885CYP2C19 4608/4885CYP2C9 4771/4885
US-20100286178-A1 COMPOUNDS AND USES THEREOF BRAF, RAF1, FER BRAF 1/4885CYP2C19 3265/4885CYP2C9 2194/4885
US-11986531-B2 Compounds and methods for the targeted degradation of rapidly accelerated fibrosarcoma polypeptides CRBN, ARAF, VHL BRAF 4/4885CYP2C19 4850/4885CYP2C9 4808/4885
US-20260115296-A1 COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF RAPIDLY ACCELERATED FIBROSARCOMA POLYPEPTIDES CRBN, VHL, ADRM1 BRAF 8/4885CYP2C19 4873/4885CYP2C9 4810/4885

“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.