SCHEMBL1110476

SCHEMBL1110476

O=C(Nc1cc(C(F)(F)F)ccc1N1CCCCC1)c1ccncc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SRPK1 Q96SB4 2/20 1.00
KDR P35968 2/20 1.00
SRPK2 P78362 1/20 1.00
SRPK3 Q9UPE1 1/20 1.00
MAPT P10636 5/20 0.65
ALDH1A1 P00352 4/20 0.65
TSHR P16473 2/20 0.65
MEN1 O00255 1/20 0.65
KMT2A Q03164 1/20 0.65
LMNA P02545 1/20 0.64
HSD17B10 Q99714 2/20 0.64
HPGD P15428 1/20 0.64
NPSR1 Q6W5P4 1/20 0.64
CYP1A2 P05177 1/20 0.63
CYP2C9 P11712 1/20 0.63
CYP2C19 P33261 1/20 0.63
POLB P06746 2/20 0.62
TEK Q02763 4/20 0.60
LCK P06239 2/20 0.60
RXFP1 Q9HBX9 1/20 0.59

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
SCHEMBL1110544 1.00 SRPK1 (1.00) SRPK1KDRSRPK2SRPK3MAPT
SCHEMBL3485927 1.00 SRPK1 (1.00) SRPK1KDRSRPK2SRPK3MAPT
SCHEMBL3485920 0.99 SRPK1 (0.98) SRPK1KDRSRPK2SRPK3MAPT
SCHEMBL1110642 0.89 SRPK1 (0.80) SRPK1KDRSRPK2SRPK3MAPT
SCHEMBL13540499 0.88 SRPK1 (0.79) SRPK1KDRSRPK2SRPK3ALDH1A1
SCHEMBL12765717 0.88 SRPK1 (0.78) SRPK1KDRSRPK2SRPK3MAPT
SCHEMBL3485129 0.88 SRPK1 (0.78) SRPK1KDRSRPK2SRPK3MAPT
SCHEMBL3485680 0.88 POLB (0.81) SRPK1KDRSRPK2SRPK3MAPT
SCHEMBL1110612 0.87 SRPK1 (0.77) SRPK1KDRSRPK2SRPK3MAPT
SCHEMBL20198561 0.87 KDR (0.77) SRPK1KDRSRPK2SRPK3MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260053809-A1 MOLECULAR THERAPEUTIC STRATEGY COMBINING IDELALISIB AND SRPIN340 TO TREAT ADVANCE SOLID TUMORS UNIV OF MARYLAND EASTERN SHORE (US) 2026-02-26 US claimed
EP-4361136-A1 COMPOUND FOR THE TREATMENT OF GLIOBLASTOMA Universidad De Córdoba (ES) 2024-05-01 EP claimed
US-20220380765-A1 TARGETING NONSENSE-MEDIATED DECAY TO ACTIVATE P53 PATHWAY FOR THE TREATMENT OF CANCER BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2022-12-01 US claimed
US-11499197-B2 Prognosis method of multiple myeloma CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2022-11-15 US claimed
EP-3432886-B1 PIM KINASE INHIBITORS IN COMBINATION WITH RNA SPLICING MODULATORS/INHIBITORS FOR TREATMENT OF CANCERS UNIV MARYLAND (US) 2021-06-02 EP claimed
US-10842785-B2 PIM kinase inhibitors in combination with RNA splicing modulators/inhibitors for treatment of cancers THE UNIVERSITY OF MARYLAND, BALTIMORE COUNTY (US) 2020-11-24 US claimed
US-20200046689-A1 PIM KINASE INHIBITORS IN COMBINATION WITH RNA SPLICING MODULATORS/INHIBITORS FOR TREATMENT OF CANCERS UNIV MARYLAND (US) 2020-02-13 US claimed
US-20190076416-A1 PIM KINASE INHIBITORS IN COMBINATION WITH RNA SPLICING MODULATORS/INHIBITORS FOR TREATMENT OF CANCERS UNIV MARYLAND (US) 2019-03-14 US claimed
EP-3432886-A1 PIM KINASE INHIBITORS IN COMBINATION WITH RNA SPLICING MODULATORS/INHIBITORS FOR TREATMENT OF CANCERS University of Maryland, Baltimore County (US) 2019-01-30 EP claimed
WO-2017165495-A1 PIM KINASE INHIBITORS IN COMBINATION WITH RNA SPLICING MODULATORS/INHIBITORS FOR TREATMENT OF CANCERS UNIVERSITY OF MARYLAND, BALTIMORE COUNTY (US) 2017-09-28 WO claimed
EP-4048809-B1 SYSTEMS AND METHODS FOR PREDICTING THERAPEUTIC SENSITIVITY TEMPUS AI INC (US) 2026-05-27 EP disclosed
EP-4729940-A2 LARGE SCALE ORGANOID ANALYSIS Tempus AI, Inc. (US) 2026-04-22 EP disclosed
US-20260053809-A1 MOLECULAR THERAPEUTIC STRATEGY COMBINING IDELALISIB AND SRPIN340 TO TREAT ADVANCE SOLID TUMORS UNIV OF MARYLAND EASTERN SHORE (US) 2026-02-26 US disclosed
US-20260053809-A1 MOLECULAR THERAPEUTIC STRATEGY COMBINING IDELALISIB AND SRPIN340 TO TREAT ADVANCE SOLID TUMORS UNIV OF MARYLAND EASTERN SHORE (US) 2026-02-26 US disclosed
US-20260053809-A1 MOLECULAR THERAPEUTIC STRATEGY COMBINING IDELALISIB AND SRPIN340 TO TREAT ADVANCE SOLID TUMORS UNIV OF MARYLAND EASTERN SHORE (US) 2026-02-26 US disclosed
US-20070135367-A1 Broad spectrum antiviral including against SARS (severe acute respiratory syndrome), DNA viruses and herpes viruses; Ser-Arg (SR), SR proteins are RNA-binding proteins; compounds are SRPK inhibitors such as 1-piperidino-2-(pyridin-4-ylcarbonylamino)-4-trifluoromethylbenzene HAGIWARA, MASATOSHI (JP) 2007-06-14 US disclosed
US-20070135367-A1 Broad spectrum antiviral including against SARS (severe acute respiratory syndrome), DNA viruses and herpes viruses; Ser-Arg (SR), SR proteins are RNA-binding proteins; compounds are SRPK inhibitors such as 1-piperidino-2-(pyridin-4-ylcarbonylamino)-4-trifluoromethylbenzene HAGIWARA, MASATOSHI (JP) 2007-06-14 US disclosed
US-20070135367-A1 Broad spectrum antiviral including against SARS (severe acute respiratory syndrome), DNA viruses and herpes viruses; Ser-Arg (SR), SR proteins are RNA-binding proteins; compounds are SRPK inhibitors such as 1-piperidino-2-(pyridin-4-ylcarbonylamino)-4-trifluoromethylbenzene HAGIWARA, MASATOSHI (JP) 2007-06-14 US disclosed
CN-1921885-A Method for controlling phosphorylation of SR protein and antiviral agent comprising SR protein activity controller as active ingredient HAGIWARA MASATOSHI (JP) 2007-02-28 CN disclosed
EP-1712242-A1 METHOD OF REGULATING PHOSPHORYLATION OF SR PROTEIN AND ANTIVIRAL AGENTS COMPRISING SR PROTEIN ACTIVITY REGULATOR AS THE ACTIVE INGREDIENT HAGIWARA, Masatoshi (JP) 2006-10-18 EP 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 (2 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-20070135367-A1 Broad spectrum antiviral including against SARS (severe acute respiratory syndrome), DNA viruses and herpes viruses; Ser-Arg (SR), SR proteins are RNA-binding proteins; compounds are SRPK inhibitors such as 1-piperidino-2-(pyridin-4-ylcarbonylamino)-4-trifluoromethylbenzene SRPK1, SARS1, SRPK3 SRPK1 1/4885KDR 2410/4885SRPK2 4/4885
US-20260053809-A1 MOLECULAR THERAPEUTIC STRATEGY COMBINING IDELALISIB AND SRPIN340 TO TREAT ADVANCE SOLID TUMORS PIK3R4, SRPK3, PIK3R5 SRPK1 4/4885KDR 1523/4885SRPK2 6/4885

“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.