SCHEMBL9192176

SCHEMBL9192176

O=C1c2ccccc2C(=O)c2c1ccc(C(=O)O)c2[N+](=O)[O-]

nearest known ligand 0.72

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 6/20 0.72
NPC1 O15118 2/20 0.72
RAB9A P51151 2/20 0.72
HPGD P15428 1/20 0.67
ALDH1A1 P00352 7/20 0.63
CYP3A4 P08684 3/20 0.63
TSHR P16473 2/20 0.63
MAPT P10636 11/20 0.60
MEN1 O00255 5/20 0.60
KMT2A Q03164 5/20 0.60
LMNA P02545 5/20 0.60
MAPK1 P28482 4/20 0.60
POLB P06746 2/20 0.60
THRB P10828 1/20 0.60
RECQL P46063 1/20 0.60
L3MBTL1 Q9Y468 1/20 0.58
KDM4E B2RXH2 1/20 0.56
MMP14 P50281 1/20 0.56
PKM P14618 1/20 0.52
CYP2D6 P10635 3/20 0.51

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
Hydrochloric Acid SCHEMBL11776089 0.98 SMN1; SMN2 (0.71) SMN1; SMN2NPC1RAB9AHPGDALDH1A1
SCHEMBL11330090 0.88 SMN1; SMN2 (0.69) SMN1; SMN2NPC1RAB9AHPGDALDH1A1
SCHEMBL11776076 0.88 SMN1; SMN2 (0.69) SMN1; SMN2NPC1RAB9AHPGDALDH1A1
SCHEMBL11317722 0.85 SMN1; SMN2 (0.62) SMN1; SMN2NPC1RAB9AHPGDALDH1A1
SCHEMBL11330097 0.84 SMN1; SMN2 (0.68) SMN1; SMN2NPC1RAB9AHPGDALDH1A1
SCHEMBL11327656 0.84 SMN1; SMN2 (1.00) SMN1; SMN2NPC1RAB9AHPGDALDH1A1
SCHEMBL7827861 0.82 SMN1; SMN2 (0.52) SMN1; SMN2NPC1RAB9AHPGDALDH1A1
SCHEMBL11325695 0.81 SMN1; SMN2 (1.00) SMN1; SMN2NPC1RAB9AHPGDALDH1A1
SCHEMBL11318200 0.81 SMN1; SMN2 (0.67) SMN1; SMN2NPC1RAB9AHPGDALDH1A1
SCHEMBL11327907 0.81 SMN1; SMN2 (0.67) SMN1; SMN2NPC1RAB9AHPGDALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0530559-B1 Process for the preparation of 1-nitroanthraquinone-2-carboxylic acid BASF AG (DE) 1995-10-18 EP claimed
US-5245058-A PREPARATION OF 1-NITROANTHRAQUINONE-2-CARBOXYLIC ACIDS BASF AKTIENGESELLSCHAFT (DE) 1993-09-14 US claimed
EP-0371362-B1 PROCESS FOR THE PREPARATION OF 1-NITRO, 2-CARBOXY-ANTHRAQUINONE BASF Aktiengesellschaft (DE) 1993-02-03 EP claimed
US-4950756-A OXIDATION OF 2-SUBSTITUTED 1-NITROANTHRAQUINONE BASF AKTIENGESELLSCHAFT (DE) 1990-08-21 US claimed
EP-0021264-B1 PROCESS FOR THE DELIGNIFICATION OF LIGNOCELLULOSIC MATERIALS BAYER AG (DE) 1983-01-19 EP claimed
EP-0005206-B1 METHOD OF PREPARING 1,4-DIAMINOANTHRAQUINONE-2-CARBOXYLIC ACID CIBA-GEIGY AG (CH) 1981-04-01 EP claimed
US-4250102-A Process for the manufacture of aminohydroxyanthraquinones CIBA-GEIGY AG (CH) 1981-02-10 US claimed
EP-0021264-A1 Process for the delignification of lignocellulosic materials BAYER AG (DE) 1981-01-07 EP claimed
US-4243600-A Process for the manufacture of 1,4-diaminoanthraquinone-2-carboxylic acid CIBA-GEIGY AG (CH) 1981-01-06 US claimed
US-4198518-A Process for the production of 3-substituted pyrazolanthrones CIBA-GEIGY CORPORATION (US) 1980-04-15 US claimed
US-4046785-A Process for preparing aminoanthraquinones MITSUI TOATSU CHEMICALS, INC. (JA) 1977-09-06 US claimed
JP-2184657-A None JP disclosed
JP-5194329-A None JP disclosed
US-20260117284-A1 REDOX LABELED OLIGONUCLEOTIDE PROBES AND THEIR USE ABBOTT DIAGNOSTICS SCARBOROUGH INC 2026-04-30 US disclosed
EP-4556571-A2 REDOX LABELED OLIGONUCLEOTIDE PROBES AND THEIR USE Abbott Diagnostics Scarborough, Inc. (US) 2025-05-21 EP disclosed
US-4202696-A Method of removing surface tack of cured free radical polymerized resin composition using organic carbonyl compound ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1980-05-13 US disclosed
US-4198518-A Process for the production of 3-substituted pyrazolanthrones CIBA-GEIGY CORPORATION (US) 1980-04-15 US disclosed
US-4046785-A Process for preparing aminoanthraquinones MITSUI TOATSU CHEMICALS, INC. (JA) 1977-09-06 US disclosed
US-4016182-A Process for the production of aminoanthraquinone compounds SANDOZ LTD. (CH) 1977-04-05 US disclosed
US-4006171-A FROM NITROANTHRAQUINONE AND HALOGEN BAYER AKTIENGESELLSCHAFT (DT) 1977-02-01 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 (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-20260117284-A1 REDOX LABELED OLIGONUCLEOTIDE PROBES AND THEIR USE POLRMT, SQOR, MTHFD1 SMN1; SMN2 3703/4885NPC1 4809/4885RAB9A 4868/4885

“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.