SCHEMBL794075

SCHEMBL794075

O=Cc1n[nH]c2cc(Br)ccc12

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDPK1 O15530 2/20 0.58
JAK2 O60674 2/20 0.58
DYRK1A Q13627 6/20 0.49
CYP2A6 P11509 1/20 0.49
GSK3B P49841 2/20 0.44
AXL P30530 1/20 0.43
CHEK1 O14757 4/20 0.43
KDR P35968 3/20 0.43
IDO1 P14902 1/20 0.43
METAP2 P50579 2/20 0.42
PIM3 Q86V86 2/20 0.41
DCLK1 O15075 1/20 0.40
PRKD3 O94806 1/20 0.40
MAP4K4 O95819 1/20 0.40
CHEK2 O96017 1/20 0.40
CSF1R P07333 1/20 0.40
FER P16591 1/20 0.40
CDK2 P24941 1/20 0.40
MARK3 P27448 1/20 0.40
FLT4 P35916 1/20 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
SCHEMBL29497531 1.00 PDPK1 (0.58) PDPK1JAK2DYRK1ACYP2A6GSK3B
SCHEMBL660142 0.86 PDPK1 (0.58) PDPK1JAK2DYRK1ACYP2A6GSK3B
SCHEMBL3538242 0.80 TTK (0.54) CYP2A6CHEK1KDRCDK2
SCHEMBL23087789 0.79 PRMT5 (0.44) PDPK1JAK2DYRK1ACYP2A6GSK3B
SCHEMBL29915098 0.79 PRMT5 (0.44) PDPK1JAK2DYRK1ACYP2A6GSK3B
SCHEMBL15304355 0.79 ITK (0.46) CHEK1KDRPIM3CDK2PIM1
SCHEMBL3537177 0.79 MAP2K4 (0.51) CHEK1CDK2
SCHEMBL5211222 0.79 MAP2K4 (0.48) DYRK1AGSK3BCHEK1KDRCDK2
SCHEMBL29955085 0.79 ITK (0.46) CHEK1KDRPIM3CDK2PIM1
SCHEMBL29955404 0.79 PDPK1 (0.54) PDPK1JAK2GSK3BCHEK1KDR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4736854-A2 HETEROCYCLIC COMPOUNDS AS MODULATORS OF BCL6 AS LIGAND DIRECTED DEGRADERS Bristol-Myers Squibb Company (US) 2026-05-06 EP disclosed
EP-4003977-B1 PYRIDINE DERIVATIVES AS CALCIUM-ACTIVATED CHLORIDE CHANNEL MODULATORS TMEM16A LTD (GB) 2026-04-15 EP disclosed
EP-4514473-B1 HETEROCYCLIC COMPOUNDS AS MODULATORS OF BCL6 AS LIGAND DIRECTED DEGRADERS BRISTOL MYERS SQUIBB CO (US) 2026-02-18 EP disclosed
US-12545658-B2 Pyridine derivatives as calcium-activated chloride channel modulators TMEM16A LIMITED (GB) 2026-02-10 US disclosed
US-20250320183-A1 Modulators of BCL6 as Ligand Directed Degraders CELGENE CORPORATION (US) 2025-10-16 US disclosed
US-12404239-B2 Modulators of BCL6 as ligand directed degraders CELGENE CORPORATION (US) 2025-09-02 US disclosed
EP-3728199-B1 PESTICIDAL COMPOUNDS BASF SE (DE) 2025-05-14 EP disclosed
EP-4186908-B1 JAK INHIBITOR COMPOUND AND USE THEREOF HENAN MEDINNO PHARMACEUTICAL TECH CO LTD (CN) 2025-05-07 EP disclosed
US-20250114345-A1 COMPOUNDS AND COMPOSITIONS AS CBP/P300 DEGRADERS AND USES THEREOF ONCOPIA THERAPEUTICS, INC. D/B/A/ SK LIFE SCIENCE LABS 2025-04-10 US disclosed
WO-2025059429-A1 MODULATORS OF BCL6 FOR USE IN A METHOD OF TREATING A CANCER OR AN AUTOIMMUNE DISEASE BRISTOL-MYERS SQUIBB COMPANY (US) 2025-03-20 WO disclosed
US-20130165440-A1 JAK1 Inhibitors EXELIXIS, INC. (US) 2013-06-27 US disclosed
US-20130029968-A1 INDAZOLES PFIZER LIMITED (GB) 2013-01-31 US disclosed
WO-2013014567-A1 INDAZOLES PFIZER LIMITED (GB) 2013-01-31 WO disclosed
WO-2012123522-A1 6,5-HETEROCYCLIC PROPARGYLIC ALCOHOL COMPOUNDS AND USES THEREFOR F. HOFFMANN-LA ROCHE AG (CH) 2012-09-20 WO disclosed
US-20120214762-A1 6,5-HETEROCYCLIC PROPARGYLIC ALCOHOL COMPOUNDS AND USES THEREFOR GENENTECH, INC. (US) 2012-08-23 US disclosed
WO-2012037132-A1 PHTALAZINE DERIVATIVES AS JAK1 INHIBITORS EXELIXIS, INC. (US) 2012-03-22 WO disclosed
WO-2012037132-A1 PHTALAZINE DERIVATIVES AS JAK1 INHIBITORS EXELIXIS, INC. (US) 2012-03-22 WO disclosed
US-20110245179-A1 Composition for Prevention or Treatment of Heart Failure PARK WOO JIN 2011-10-06 US disclosed
US-20110245179-A1 Composition for Prevention or Treatment of Heart Failure PARK WOO JIN 2011-10-06 US disclosed
US-20110245179-A1 Composition for Prevention or Treatment of Heart Failure PARK WOO JIN 2011-10-06 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 (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-20130029968-A1 INDAZOLES CYP11B2, CYP11B1, IL33 PDPK1 1902/4885JAK2 1289/4885DYRK1A 3287/4885
US-20110245179-A1 Composition for Prevention or Treatment of Heart Failure ATP2A3, ATP2A1, MYLK2 PDPK1 193/4885JAK2 3858/4885DYRK1A 3065/4885
US-12545658-B2 Pyridine derivatives as calcium-activated chloride channel modulators CACNA1E, CACNA1D, CACNA1B PDPK1 1429/4885JAK2 3045/4885DYRK1A 4217/4885
US-20250114345-A1 COMPOUNDS AND COMPOSITIONS AS CBP/P300 DEGRADERS AND USES THEREOF EP300, CREBBP, HDAC1 PDPK1 2923/4885JAK2 4120/4885DYRK1A 4137/4885
US-12404239-B2 Modulators of BCL6 as ligand directed degraders BCL6, BCL6B, BCL3 PDPK1 3178/4885JAK2 1051/4885DYRK1A 1618/4885
US-20130165440-A1 JAK1 Inhibitors JAK1, JAK2, JAK3 PDPK1 783/4885JAK2 2/4885DYRK1A 752/4885
US-20120214762-A1 6,5-HETEROCYCLIC PROPARGYLIC ALCOHOL COMPOUNDS AND USES THEREFOR NFKB1, NFRKB, NFKBIA PDPK1 1254/4885JAK2 1197/4885DYRK1A 2084/4885
US-20250320183-A1 Modulators of BCL6 as Ligand Directed Degraders BCL6, BCL6B, BCL3 PDPK1 3178/4885JAK2 1051/4885DYRK1A 1618/4885

“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.