SCHEMBL6439758

SCHEMBL6439758

Cc1cc(C(N)=O)cn1C

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BRD4 O60885 3/20 0.45
BRD9 Q9H8M2 1/20 0.45
PARP1 P09874 3/20 0.41
PARP15 Q460N3 1/20 0.41
PARP10 Q53GL7 1/20 0.41
HSD17B10 Q99714 3/20 0.39
KDM4E B2RXH2 2/20 0.39
ALDH1A1 P00352 2/20 0.39
BRPF1 P55201 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
LMNA P02545 1/20 0.39
ACHE P22303 1/20 0.39
PKM P14618 1/20 0.36
CCNC P24863 1/20 0.36
CDK8 P49336 1/20 0.36
MKNK1 Q9BUB5 1/20 0.35
MKNK2 Q9HBH9 1/20 0.35
POLB P06746 1/20 0.34
CYP3A4 P08684 1/20 0.34
MAPT P10636 1/20 0.34

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
Malic Acid SCHEMBL27610482 0.81 SMN1; SMN2 (0.43) BRD4BRD9PARP1PARP15PARP10
SCHEMBL6438124 0.80 TPMT (0.44) HSD17B10KDM4EALDH1A1SMN1; SMN2POLB
SCHEMBL18315117 0.78 PRSS1 (0.46) LMNAPKMBLMHDAC3HDAC4
SCHEMBL20726642 0.78 BRD4 (0.66) BRD4BRD9PARP1PARP15PARP10
SCHEMBL34469515 0.77 BRD4 (0.40) BRD4BRD9PARP1PARP15PARP10
SCHEMBL24158944 0.75 CYP2C9 (0.50) BRD4BRD9PARP1PARP15PARP10
SCHEMBL18092436 0.75 CA1 (0.45) HSD17B10KDM4EALDH1A1SMN1; SMN2LMNA
SCHEMBL4848806 0.74 ATM (0.57) BRD4BRD9PARP1PARP15PARP10
SCHEMBL18584635 0.74 BRD4 (0.49) BRD4BRD9PARP1PARP15PARP10
SCHEMBL4848799 0.74 BRD4 (0.38) BRD4BRD9PARP1PARP15PARP10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101939314-B Polymorphic forms of a 3-pyrrole substituted 2-indolinone MEDICHEM SA 2014-04-02 CN claimed
CN-102740888-A Antibodies to IL-6 and use there ALDER BIOPHARMACEUTICALS INC 2012-10-17 CN claimed
CN-101939314-A Polymorphic forms of a 3-pyrrole substituted 2-indolinone MEDICHEM SA 2011-01-05 CN claimed
CN-100439360-C Crystal of malate comprising N- [2- (diethylamino) ethyl ] -5- [ (5-fluoro-2-oxo-3H-indol-3-ylidene) methyl ] -2, 4-dimethyl-1H-pyrrole-3-carboxamide, method for preparing same and composition thereof UPJOHN CO (US) 2008-12-03 CN claimed
CN-100432072-C Salts and polymorphs of a pyrrole-substituted indolinone compound PHARMACIA & UPJOHN CO LLC (US) 2008-11-12 CN claimed
CN-100364991-C Crystals including a malic acid salt of a 3-pyrrole substituted 2-indolinone, and compositions thereof UPJOHN CO (US) 2008-01-30 CN claimed
CN-1863796-A Salts and polymorphs of a pyrrole-substituted indolinone compound PHARMACIA & UPJOHN CO LLC (US) 2006-11-15 CN claimed
CN-1789264-A Crystals including a malic acid salt of a 3-pyrrole substituted 2-indolinone, and compositions thereof UPJOHN CO (US) 2006-06-21 CN claimed
EP-1542734-A1 ISOTOPICALLY LABELLED INDOLINONE DERIVATIVES AND PROCESS FOR THEIR PREPARATION Pharmacia Italia S.p.A. (IT) 2005-06-22 EP claimed
CN-1543462-A Crystal of malate comprising N- [ 2- (diethylamino) ethyl ] -5- [ (5-fluoro-2-oxo-3H-indol-3-ylidene) methyl ] -2, 4-dimethyl-1H-pyrrole-3-carboxamide, method for preparing same and composition thereof �������Ŷ���Լ��������˾ 2004-11-03 CN claimed
WO-2004012776-A1 ISOTOPICALLY LABELLED INDOLINONE DERIVATIVES AND PROCESS FOR THEIR PREPARATION PHARMACIA ITALIA S.P.A. (IT) 2004-02-12 WO claimed
US-12570645-B2 Uses of p53 x-ray co-crystal structures PMV PHARMACEUTICALS, INC. (US) 2026-03-10 US disclosed
US-20260027097-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION PMV PHARMACEUTICALS INC (US) 2026-01-29 US disclosed
US-20250319063-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT P53 FUNCTION PMV PHARMACEUTICALS, INC. 2025-10-16 US disclosed
US-12419880-B2 Companion diagnostic tool for mutant p53 reactivating compounds PMV PHARMACEUTICALS, INC. (US) 2025-09-23 US disclosed
EP-1542734-A1 ISOTOPICALLY LABELLED INDOLINONE DERIVATIVES AND PROCESS FOR THEIR PREPARATION Pharmacia Italia S.p.A. (IT) 2005-06-22 EP disclosed
CN-1543462-A Crystal of malate comprising N- [ 2- (diethylamino) ethyl ] -5- [ (5-fluoro-2-oxo-3H-indol-3-ylidene) methyl ] -2, 4-dimethyl-1H-pyrrole-3-carboxamide, method for preparing same and composition thereof �������Ŷ���Լ��������˾ 2004-11-03 CN disclosed
WO-2004012776-A1 ISOTOPICALLY LABELLED INDOLINONE DERIVATIVES AND PROCESS FOR THEIR PREPARATION PHARMACIA ITALIA S.P.A. (IT) 2004-02-12 WO disclosed
EP-1370554-A1 3-(4-AMIDOPYRROL-2-YLMETHYLIDENE)-2-INDOLINONE DERIVATIVES AS PROTEIN KINASE INHIBITORS PHARMACIA & UPJOHN COMPANY (US) 2003-12-17 EP disclosed
WO-2002066463-A1 3-(4-AMIDOPYRROL-2-YLMETHLIDENE)-2-INDOLINONE DERIVATIVES AS PROTEIN KINASE INHIBITORS PHARMACIA & UPJOHN COMPANY (US) 2002-08-29 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 (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-20250319063-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT P53 FUNCTION TP53, TP53BP1, KRAS BRD4 1272/4885BRD9 3362/4885PARP1 865/4885
US-20260027097-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION TP53, TP53BP1, BRCA1 BRD4 324/4885BRD9 185/4885PARP1 457/4885
US-12570645-B2 Uses of p53 x-ray co-crystal structures TP53, TP53BP1, ERCC2 BRD4 2324/4885BRD9 1744/4885PARP1 694/4885
US-12419880-B2 Companion diagnostic tool for mutant p53 reactivating compounds TP53, TP53BP1, KRAS BRD4 1089/4885BRD9 2090/4885PARP1 928/4885

“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.