SCHEMBL104409

SCHEMBL104409

Cc1ccc(C(=O)Oc2ccccc2)cc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP10 Q53GL7 1/20 0.59
PRSS1 P07477 2/20 0.58
ACR P10323 2/20 0.58
MAPT P10636 2/20 0.58
SMN1; SMN2 Q16637 2/20 0.58
TMPRSS15 P98073 2/20 0.57
USP2 O75604 1/20 0.57
KMT2A Q03164 5/20 0.56
TDP1 Q9NUW8 2/20 0.56
ALDH1A1 P00352 2/20 0.56
L3MBTL1 Q9Y468 1/20 0.56
PKM P14618 1/20 0.56
CES2 O00748 1/20 0.55
CES1 P23141 1/20 0.55
NSD2 O96028 1/20 0.55
NPC1 O15118 2/20 0.54
RAB9A P51151 1/20 0.54
MEN1 O00255 1/20 0.53
CYP1A2 P05177 1/20 0.53
CYP2C9 P11712 1/20 0.53

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
SCHEMBL11584711 0.98 PARP10 (0.62) PARP10PRSS1ACRMAPTSMN1; SMN2
SCHEMBL13415306 0.94 SMN1; SMN2 (0.56) PARP10PRSS1ACRMAPTSMN1; SMN2
SCHEMBL15382236 0.94 PARP10 (0.68) PARP10PRSS1ACRMAPTSMN1; SMN2
SCHEMBL26038899 0.94 PARP10 (0.68) PARP10PRSS1ACRMAPTSMN1; SMN2
SCHEMBL8638980 0.93 PARP10 (0.57) PARP10PRSS1ACRMAPTSMN1; SMN2
Formic Acid SCHEMBL18406223 0.93 PARP10 (0.53) PARP10PRSS1ACRMAPTSMN1; SMN2
SCHEMBL26038990 0.93 SMN1; SMN2 (0.58) PARP10PRSS1ACRMAPTSMN1; SMN2
Benzoic Acid 4-Methylphenyl Ester SCHEMBL1546372 0.92 KMT2A (0.66) PARP10PRSS1ACRMAPTSMN1; SMN2
SCHEMBL11111888 0.91 PARP10 (0.56) PARP10PRSS1ACRMAPTSMN1; SMN2
SCHEMBL15014171 0.90 VCP (0.53) PARP10PRSS1ACRMAPTSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250129015-A1 HALOGENATED BENZYLIDINE DERIVATIVES Renovel Innovations, Inc. (US) 2025-04-24 US claimed
WO-2023212597-A1 CARBON DIOXIDE CAPTURE AND UTILIZATION AS A CLEAN FEEDSTOCK MICHIGAN TECHNOLOGICAL UNIVERSITY (US) 2023-11-02 WO claimed
CN-111033777-B Dielectric layer comprising copolymer with mesogenic units PPG工业俄亥俄公司 2023-08-08 CN claimed
US-20230107812-A1 HALOGENATED BENZYLIDINE DERIVATIVES Renovel Innovations, Inc. 2023-04-06 US claimed
CN-103236542-A Preparation method for lithium-sulfur battery positive electrode material adopting metal-organic framework material as sulfur carrier UNIV ZHEJIANG 2013-08-07 CN claimed
CN-1109683-C 2-arylbenzo [ b ] thiophenes for the treatment of estrogen deficiency syndrome LILLY CO ELI (US) 2003-05-28 CN claimed
CN-1278811-A 2-arylbenzo [ b ] thiophenes for the treatment of estrogen deficiency syndrome LILLY CO ELI (US) 2001-01-03 CN claimed
US-5789576-A DIASTEREOSPECIFIC DIMERIZATION USING ALKOXYMAGNESIUM HALIDE REACTANT; USED FOR SOLID PHASE SYNTHESIS OF ANTISENSE OLIGONUCLEOTIDES GENTA INCORPORATED (US) 1998-08-04 US claimed
US-20250188626-A1 CARBON DIOXIDE CAPTURE AND UTILIZATION AS A CLEAN FEEDSTOCK UNIV MICHIGAN TECH (US) 2025-06-12 US disclosed
CN-119708924-A Ink, ink preparation method and ink-jet printing method 广东聚华印刷显示技术有限公司 2025-03-28 CN disclosed
EP-3869268-B1 MATERIAL FOR FORMING ORGANIC FILM, PATTERNING PROCESS, AND POLYMER SHINETSU CHEMICAL CO (JP) 2024-01-17 EP disclosed
US-11858952-B2 Compound and color conversion film comprising same LG CHEM, LTD. (KR) 2024-01-02 US disclosed
US-11858952-B2 Compound and color conversion film comprising same LG CHEM, LTD. (KR) 2024-01-02 US disclosed
WO-2023212597-A1 CARBON DIOXIDE CAPTURE AND UTILIZATION AS A CLEAN FEEDSTOCK MICHIGAN TECHNOLOGICAL UNIVERSITY (US) 2023-11-02 WO disclosed
US-4609928-A LEUCO DYES, COLOR DEVELOPERS, BISHENOL, P-HYDROXYBENZOIC ACID ESTER, POROSITY, FILLERS RICOH COMPANY, LTD. (JP) 1986-09-02 US disclosed
US-4575734-A LEVCO DYES RICOH COMPANY, LTD. (JP) 1986-03-11 US disclosed
US-4562448-A Heat-sensitive transfer medium RICOH CO., LTD. (JP) 1985-12-31 US disclosed
US-4547788-A SHEET HAVING LAYER CONTAINING LEVCO DYE; ACCEPTOR SHEET CONTAININGCOLORING AGENT; POROUS FILLER RICOH COMPANY, LTD. (JP) 1985-10-15 US disclosed
US-4479138-A PHENYL BENZOIC ESTER TO INCREASE SENSITIVITY FUJI PHOTO FILM CO., LTD. (JP) 1984-10-23 US disclosed
US-3993437-A Process for the dyeing of polyamide fibers with sulphur dyestuffs CASSELLA FARBWERKE MAINKUR AKTIENGESELLSCHAFT (DT) 1976-11-23 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 (3 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-20250129015-A1 HALOGENATED BENZYLIDINE DERIVATIVES BRD2, MPO, BRD9 PARP10 783/4885PRSS1 2117/4885ACR 889/4885
US-11858952-B2 Compound and color conversion film comprising same BLVRB, CDYL, CRY1 PARP10 1789/4885PRSS1 3964/4885ACR 2726/4885
US-20230107812-A1 HALOGENATED BENZYLIDINE DERIVATIVES BRD2, MPO, BRD9 PARP10 783/4885PRSS1 2117/4885ACR 889/4885

“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.