SCHEMBL3652106

SCHEMBL3652106

COC(=O)C1C=C(C(F)(F)F)CN1C(=O)OC(C)(C)C

nearest known ligand 0.40

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PTPN1 P18031 2/20 0.40
NR1H2 P55055 3/20 0.36
NR1H3 Q13133 1/20 0.36
PDE4B Q07343 1/20 0.35
MAPT P10636 1/20 0.34
STS P08842 1/20 0.34
CETP P11597 1/20 0.34
CCNT1 O60563 1/20 0.33
CDK9 P50750 1/20 0.33
ALDH1A1 P00352 1/20 0.33
EPHX2 P34913 1/20 0.33
NPC1 O15118 1/20 0.33
TACR1 P25103 1/20 0.33
UCHL1 P09936 1/20 0.33
USP30 Q70CQ3 1/20 0.33
ESR2 Q92731 1/20 0.33
POLB P06746 1/20 0.32

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
SCHEMBL3652108 1.00 PTPN1 (0.40) PTPN1NR1H2NR1H3PDE4BMAPT
SCHEMBL15718620 0.86 HSD17B10 (0.36) NR1H2MAPTSTSTACR1UCHL1
SCHEMBL27017483 0.83 PTPN1 (0.41) PTPN1NR1H2NR1H3PDE4BCCNT1
SCHEMBL2381393 0.82 PTPN1 (0.42) PTPN1NR1H2NR1H3PDE4BALDH1A1
SCHEMBL18435493 0.82 PTPN1 (0.42) PTPN1NR1H2NR1H3PDE4BALDH1A1
SCHEMBL24645524 0.82 PTPN1 (0.42) PTPN1NR1H2NR1H3PDE4BALDH1A1
SCHEMBL18400274 0.82 PTPN1 (0.42) PTPN1NR1H2NR1H3PDE4BALDH1A1
SCHEMBL2381395 0.82 PTPN1 (0.42) PTPN1NR1H2NR1H3PDE4BALDH1A1
SCHEMBL17236235 0.80 PDK1 (0.41) TACR1
SCHEMBL2381288 0.80 PTPN1 (0.41) PTPN1NR1H2NR1H3PDE4BMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025264645-A1 SODIUM CHANNEL BLOCKING COMPOUNDS, DERIVATIVES THEREOF, AND METHODS OF THEIR USE LATIGO BIOTHERAPEUTICS, INC. (US) 2025-12-26 WO disclosed
US-9845326-B2 Substituted 3,4-dihydropyrrolo[1,2-A]pyrazines as beta-secretase (BACE) inhibitors JANSSEN PHARMACEUTICA NV (BE) 2017-12-19 US disclosed
EP-2683721-B1 3,4-DIHYDRO-PYRROLO[1,2-a]PYRAZIN-1-YLAMINE DERIVATIVES USEFUL AS INHIBITORS OF BETA-SECRETASE (BACE) JANSSEN PHARMACEUTICA NV (BE) 2015-01-28 EP disclosed
WO-2012120023-A1 3,4-DIHYDRO-PYRROLO[1,2-a]PYRAZIN-1-YLAMINE DERIVATIVES USEFUL AS INHIBITORS OF BETA-SECRETASE (BACE) JANSSEN PHARMACEUTICA NV (BE) 2012-09-13 WO disclosed
US-7691843-B2 N-hydroxyamide derivatives possessing antibacterial activity PFIZER INC. (US) 2010-04-06 US disclosed
US-20080058304-A1 N-hydroxyamide derivatives possessing antibacterial activity VICURON HOLDINGS LLC 2008-03-06 US disclosed
EP-1539744-A4 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY VICURON PHARM INC (US) 2007-06-06 EP disclosed
EP-1539744-A2 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY Vicuron Pharmaceuticals, Inc. (US) 2005-06-15 EP disclosed
WO-2004007444-A2 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY VICURON PHARMACEUTICALS, INC. (US) 2004-01-22 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 (1 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-20080058304-A1 N-hydroxyamide derivatives possessing antibacterial activity AMDHD2, OGA, ENGASE PTPN1 2663/4885NR1H2 3381/4885NR1H3 3101/4885

“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.