Rucaparib

Rucaparib

SCHEMBL844585

CNCc1ccc(-c2[nH]c3cc(F)cc4c3c2CCNC4=O)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PARP1PARP2PARP3

The experimentally established mechanism targets of Rucaparib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP1 known ✓ P09874 20/20 1.00
PARP2 known ✓ Q9UGN5 9/20 1.00
PARP3 known ✓ Q9Y6F1 1/20 1.00
DYRK3 O43781 1/20 1.00
TNKS O95271 1/20 1.00
PGR P06401 1/20 1.00
CDK1 P06493 1/20 1.00
ADRB1 P08588 1/20 1.00
POLA1 P09884 1/20 1.00
PIM1 P11309 1/20 1.00
SLC6A2 P23975 1/20 1.00
ADRA1A P35348 1/20 1.00
PTGS2 P35354 1/20 1.00
CDK16 Q00536 1/20 1.00
PDE4D Q08499 1/20 1.00
KCNH2 Q12809 1/20 1.00
DYRK1A Q13627 1/20 1.00
PARP15 Q460N3 1/20 1.00
PARP14 Q460N5 1/20 1.00
PARP10 Q53GL7 1/20 1.00

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
Rucaparib SCHEMBL29351768 1.00 PARP1 (1.00) PARP1PARP2DYRK3TNKSPGR
Rucaparib SCHEMBL5746065 0.99 PARP1 (0.98) PARP1PARP2DYRK3TNKSPGR
Rucaparib SCHEMBL29392034 0.99 PARP1 (0.98) PARP1PARP2DYRK3TNKSPGR
Rucaparib SCHEMBL5747917 0.95 PARP1 (0.90) PARP1PARP2DYRK3TNKSPGR
Rucaparib SCHEMBL29379028 0.95 PARP1 (1.00) PARP1PARP2DYRK3TNKSPGR
Rucaparib SCHEMBL844872 0.95 PARP1 (1.00) PARP1PARP2DYRK3TNKSPGR
Rucaparib SCHEMBL6701932 0.95 PARP1 (0.90) PARP1PARP2DYRK3TNKSPGR
Rucaparib SCHEMBL30413070 0.93 PARP1 (0.87) PARP1PARP2DYRK3TNKSPGR
Rucaparib SCHEMBL6702365 0.92 PARP1 (0.84) PARP1PARP2DYRK3TNKSPGR
SCHEMBL25150522 0.90 PARP1 (0.81) PARP1PARP2DYRK3TNKSPGR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3182975-B1 HIGH DOSAGE STRENGTH TABLETS OF RUCAPARIB PHARMA& SCHWEIZ GMBH (CH) 2025-10-01 EP claimed
EP-2534153-B2 SALTS AND POLYMORPHS OF 8-FLUORO-2-{4-[(METHYLAMINO}METHYL]PHENYL}-1,3,4,5-TETRAHYDRO-6H-AZEPINO[5,4,3-CD]INDOL-6-ONE PFIZER (US) 2024-05-22 EP claimed
EP-4166558-A1 SALTS AND POLYMORPHS OF 8-FLUORO-2-{4- [(METHYLAMINO)METHYL]PHENYL}-1 ,3,4,5-TETRAHYDRO-6H-AZEPINO[5,4,3- CD]INDOL-6-ONE Pfizer Inc. (US) 2023-04-19 EP claimed
US-11352362-B2 Polymorph of rucaparib camsylate SHANGHAI BEGREAT PHARMATECH (CN) 2022-06-07 US claimed
US-20200291036-A1 POLYMORPH OF RUCAPARIB CAMSYLATE AND PREPARATION METHOD THEREOF AND USE OF SAME SHANGHAI BEGREAT PHARMATECH (CN) 2020-09-17 US claimed
US-10709724-B2 Methods of treating mitochondrial dysfunction ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE (EPFL) (CH) 2020-07-14 US claimed
US-20190247371-A1 METHODS FOR TREATING SMALL CELL LUNG CANCERS BY USING PHARMACEUTICAL COMPOSITIONS OR COMBINATIONS COMPRISING INDOLIZINO[6,7-B]INDOLE DERIVATIVES ACADEMIA SINICA (TW) 2019-08-15 US claimed
EP-3150610-B1 SALTS AND POLYMORPHS OF 8-FLUORO-2-{4-[(METHYLAMINO}METHYL]PHENYL}-1,3,4,5-TETRAHYDRO-6H-AZEPINO[5,4,3-CD]INDOL-6-ONE PFIZER (US) 2019-07-31 EP claimed
EP-3515437-A1 METHODS FOR TREATING SMALL CELL LUNG CANCERS BY USING PHARMACEUTICAL COMPOSITIONS OR COMBINATIONS COMPRISING INDOLIZINO (6,7-B) INDOLE DERIVATIVES Academia Sinica (TW) 2019-07-31 EP claimed
US-10278974-B2 Salts and polymorphs of 8-fluoro-2-{4-[(methylamino)methyl]phenyl}-1,3,4,5-tetrahydro-6H-azepino[5,4,3-cd]indol-6-one PFIZER INC. (US) 2019-05-07 US claimed
US-7268126-B2 Polymorphic and amorphous forms of the phosphate salt of 8-fluoro-2-{4-[(methylamino)methyl]phenyl}-1,3,4,5-tetrahydro-6H-azepino[5,4,3-ce]indol-6-one AGOURON PHARMACEUTICALS, INC. (US) 2007-09-11 US claimed
EP-1799685-A2 POLYMORPHIC AND AMORPHOUS FORMS OF THE PHOSPHATE SALT OF 8-FLUORO-2-{4-[(METHYLAMINO)METHYL]PHENYL}-1,3,4,5-TETRAHYDRO-6H-AZEPINO[5,4,3-CD]INDOL-6-ONE Pfizer, Inc. (US) 2007-06-27 EP claimed
EP-1794163-A1 METHOD OF PREPARING POLY(ADP-RIBOSE) POLYMERASES INHIBITORS Pfizer, Inc. (US) 2007-06-13 EP claimed
US-20060100198-A1 Polymorphic and amorphous forms of the phosphate salt of 8-fluoro-2-{4-[(methylamino)methyl]phenyl}-1,3,4,5-tetrahydro-6h-azepino[5,4,3-ce]indol-6-one AGOURON PHARMACEUTICALS, INC. 2006-05-11 US claimed
WO-2006033003-A1 METHOD OF PREPARING POLY(ADP-RIBOSE) POLYMERASES INHIBITORS PFIZER, INC. (US) 2006-03-30 WO claimed
WO-2006033007-A2 POLYMORPHIC AND AMORPHOUS FORMS OF THE PHOSPHATE SALT OF 8-FLUORO-2-{4-[(METHYLAMINO)METHYL]PHENYL}-1,3,4,5-TETRAHYDRO-6H-AZEPINO[5,4,3-CD]INDOL-6-ONE PFIZER INC. (US) 2006-03-30 WO claimed
US-20060063926-A1 Method of preparing poly(ADP-ribose) polymerases inhibitors AGOURON PHARMACEUTICALS, INC. 2006-03-23 US claimed
EP-1611137-A1 SALTS OF TRICYCLIC INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASES PFIZER INC. (US) 2006-01-04 EP claimed
US-20040248879-A1 Salts of tricyclic inhibitors of poly(ADP-ribose) polymerases AGOURON PHARMACEUTICALS, INC. 2004-12-09 US claimed
WO-2004087713-A1 SALTS OF TRICYCLIC INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASES PFIZER INC. (US) 2004-10-14 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (7 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-20040248879-A1 Salts of tricyclic inhibitors of poly(ADP-ribose) polymerases PARP1, PARP2, PARP11 PARP1 1/4885PARP2 2/4885PARP3 7/4885
US-20060100198-A1 Polymorphic and amorphous forms of the phosphate salt of 8-fluoro-2-{4-[(methylamino)methyl]phenyl}-1,3,4,5-tetrahydro-6h-azepino[5,4,3-ce]indol-6-one IMPA1, INPP5B, ITPA PARP1 21/4885PARP2 411/4885PARP3 775/4885
US-20060063926-A1 Method of preparing poly(ADP-ribose) polymerases inhibitors PARP1, PARP11, PARP2 PARP1 1/4885PARP2 3/4885PARP3 10/4885
US-10278974-B2 Salts and polymorphs of 8-fluoro-2-{4-[(methylamino)methyl]phenyl}-1,3,4,5-tetrahydro-6H-azepino[5,4,3-cd]indol-6-one BRCA1, IMPA1, PARP1 PARP1 3/4885PARP2 57/4885PARP3 148/4885
US-20200291036-A1 POLYMORPH OF RUCAPARIB CAMSYLATE AND PREPARATION METHOD THEREOF AND USE OF SAME TYMP, CPSF7, CPSF6 PARP1 40/4885PARP2 299/4885PARP3 401/4885
US-20190247371-A1 METHODS FOR TREATING SMALL CELL LUNG CANCERS BY USING PHARMACEUTICAL COMPOSITIONS OR COMBINATIONS COMPRISING INDOLIZINO[6,7-B]INDOLE DERIVATIVES H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, RB1, INMT PARP1 730/4885PARP2 664/4885PARP3 711/4885
US-11352362-B2 Polymorph of rucaparib camsylate TPMT, CPSF7, TYMP PARP1 20/4885PARP2 270/4885PARP3 434/4885

“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.