SCHEMBL15215290

SCHEMBL15215290

C#Cc1cccc(Nc2nccc3c(Nc4ncccc4-c4cc(NC)ncn4)c(C)ccc23)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BRAF P15056 9/20 1.00
LCK P06239 8/20 1.00
TEK Q02763 7/20 1.00
KDR P35968 6/20 1.00
MAPK14 Q16539 2/20 1.00
RAF1 P04049 2/20 0.44
EGFR P00533 9/20 0.43
GAK O14976 3/20 0.43
FBP1 P09467 2/20 0.43
ALDH1A1 P00352 1/20 0.43
MAPT P10636 1/20 0.43
CYP1A2 P05177 1/20 0.40
CYP2D6 P10635 1/20 0.40
ALOX15 P16050 1/20 0.40
CYP2C19 P33261 1/20 0.40
HSD17B10 Q99714 1/20 0.40
CLK4 Q9HAZ1 1/20 0.40
ERBB2 P04626 2/20 0.40
RIPK2 O43353 2/20 0.40
BUB1 O43683 2/20 0.40

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
SCHEMBL2519650 0.91 BRAF (0.84) BRAFLCKTEKKDRMAPK14
SCHEMBL11889290 0.88 BRAF (0.79) BRAFLCKTEKKDRMAPK14
SCHEMBL2265173 0.88 TEK (0.78) BRAFLCKTEKKDRMAPK14
SCHEMBL11889113 0.88 BRAF (0.78) BRAFLCKTEKKDRMAPK14
SCHEMBL11888951 0.87 BRAF (0.84) BRAFLCKTEKKDRMAPK14
SCHEMBL11889511 0.87 BRAF (0.83) BRAFLCKTEKKDRMAPK14
SCHEMBL2520976 0.87 BRAF (0.77) BRAFLCKTEKKDRMAPK14
SCHEMBL11889198 0.85 BRAF (0.74) BRAFLCKTEKKDRMAPK14
SCHEMBL2517998 0.85 BRAF (0.74) BRAFLCKTEKKDRMAPK14
SCHEMBL11889039 0.85 BRAF (0.74) BRAFLCKTEKKDRMAPK14

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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11197861-B2 Methods of screening BRaf inhibitors for treating cutaneous reactions LUTRIS PHARMA LTD. (IL) 2021-12-14 US disclosed
US-20210346389-A1 USE OF TOPICAL BRAF INHIBITOR COMPOSITIONS FOR TREATMENT OF RADIATION DERMATITIS LUTRIS PHARMA LTD (IL) 2021-11-11 US disclosed
US-20200147090-A1 METHODS OF SCREENING BRAF INHIBITORS FOR TREATING CUTANEOUS REACTIONS LUTRIS PHARMA LTD (IL) 2020-05-14 US disclosed
US-10632123-B2 Use of BRaf inhibitors for treating cutaneous reactions LUTRIS PHARMA LTD. (IL) 2020-04-28 US disclosed
US-20130226549-A1 STRUCTURE-BASED FRAGMENT HOPPING FOR LEAD OPTIMIZATION AND IMPROVEMENT IN SYNTHETIC ACCESSIBILITY TSENG, YUFENG J. (TW) 2013-08-29 US disclosed
US-20130226549-A1 STRUCTURE-BASED FRAGMENT HOPPING FOR LEAD OPTIMIZATION AND IMPROVEMENT IN SYNTHETIC ACCESSIBILITY TSENG, YUFENG J. (TW) 2013-08-29 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-20210346389-A1 USE OF TOPICAL BRAF INHIBITOR COMPOSITIONS FOR TREATMENT OF RADIATION DERMATITIS BRAF, NRAS, RAF1 BRAF 1/4885LCK 9/4885TEK 1296/4885
US-10632123-B2 Use of BRaf inhibitors for treating cutaneous reactions BRAF, ERBB3, PIK3C3 BRAF 1/4885LCK 19/4885TEK 377/4885
US-11197861-B2 Methods of screening BRaf inhibitors for treating cutaneous reactions BRAF, EGFR, ERBB2 BRAF 1/4885LCK 19/4885TEK 634/4885
US-20200147090-A1 METHODS OF SCREENING BRAF INHIBITORS FOR TREATING CUTANEOUS REACTIONS BRAF, EGFR, ERBB2 BRAF 1/4885LCK 19/4885TEK 634/4885

“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.