SCHEMBL767775

SCHEMBL767775

O=[N+]([O-])c1c(O)ccc2ccccc12

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.62
CYP3A4 P08684 1/20 0.60
ESR1 P03372 1/20 0.57
ESR2 Q92731 1/20 0.57
S100A4 P26447 1/20 0.53
CTSB P07858 1/20 0.52
NCEH1 Q6PIU2 1/20 0.51
PTPN22 Q9Y2R2 1/20 0.50
ALDH1A1 P00352 1/20 0.50
KDM4E B2RXH2 1/20 0.49
MEN1 O00255 1/20 0.49
MAPT P10636 1/20 0.49
KMT2A Q03164 1/20 0.49
GPR35 Q9HC97 1/20 0.48
HPRT1 P00492 1/20 0.47
CASP6 P55212 1/20 0.47
ERN1 O75460 1/20 0.47
POLB P06746 1/20 0.47
RRM1 P23921 1/20 0.46
USP2 O75604 1/20 0.46

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
SCHEMBL27824283 0.98 TSHR (0.61) TSHRCYP3A4ESR1ESR2S100A4
SCHEMBL10719531 0.84 CYP3A4 (0.59) TSHRCYP3A4ESR1ESR2S100A4
SCHEMBL28284165 0.82 TSHR (0.48) TSHRCYP3A4ESR1ESR2NCEH1
SCHEMBL7118487 0.79 CYP3A4 (0.69) TSHRCYP3A4ESR1ESR2S100A4
SCHEMBL32681583 0.79 ESR1 (0.64) TSHRCYP3A4ESR1ESR2S100A4
SCHEMBL9482795 0.79 ESR1 (0.64) TSHRCYP3A4ESR1ESR2S100A4
SCHEMBL28420685 0.79 ESR1 (0.58) TSHRCYP3A4ESR1ESR2S100A4
SCHEMBL18347041 0.79 GPR35 (0.51) TSHRCYP3A4S100A4CTSBNCEH1
1-Naphthol SCHEMBL28227989 0.79 GPR35 (0.60) TSHRCYP3A4S100A4CTSBALDH1A1
SCHEMBL187452 0.78 TSHR (0.65) TSHRCYP3A4S100A4CTSBNCEH1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119552083-A Method for preparing 1-nitro-2-naphthol by selective nitration of 2-naphthol 常州佳德医药科技有限公司 2025-03-04 CN claimed
CN-113310962-A Rapid colorimetric fluorescent hypochlorite detection reagent 中国科学院新疆理化技术研究所 2021-08-27 CN claimed
EP-2877462-A1 PROCESSES FOR PREPARING ISOINDOLINE-1,3-DIONE COMPOUNDS Celgene Corporation (US) 2015-06-03 EP claimed
WO-2014018866-A1 PROCESSES FOR PREPARING ISOINDOLINE-1,3-DIONE COMPOUNDS CELGENE CORPORATION (US) 2014-01-30 WO claimed
US-20140031552-A1 PROCESSES FOR PREPARING ISOINDOLINE-1,3-DIONE COMPOUNDS CELGENE CORPORATION (US) 2014-01-30 US claimed
EP-1664334-B1 METHOD AND DEVICE FOR DETERMINING IF A PRODUCT IS IN CONDITION FOR USE OR CONSUMPTION CRYOLOG S A (FR) 2012-04-18 EP claimed
US-7960176-B2 Method and device for determining if a product is in condition for use or consumption CRYOLOG SA (FR) 2011-06-14 US claimed
US-20070275467-A1 Method and Device for Determining if a Product is in Condition for Use or Consumption CRYOLOG S.A. (FR) 2007-11-29 US claimed
WO-2007056569-A2 LIGHT RESPONSIVE SELF-TANNING PRODUCTS AND METHODS FOR USE SCALES-MEDEIROS VIRGINIA (US) 2007-05-18 WO claimed
CN-1894420-A Method and device for determining if a product is in condition for use or consumption CRYOLOG S A (FR) 2007-01-10 CN claimed
EP-0388660-A2 Photochromic compound SHOWA DENKO KABUSHIKI KAISHA (JP) 1990-09-26 EP claimed
US-4425404-A MULTILAYER, PROTECTIVE COATINGS MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 1984-01-10 US claimed
US-4196112-A ADDUCT OF A BUTADIENE POLYMER AN A,B-ACID, A CARBOCYCLIC ALCOHOL GELATION INHIBITOR, A HYDROPHILIC SOLVENT, A NEUTRALIZER NIPPON OIL CO., LTD. (JP) 1980-04-01 US claimed
US-4175068-A ADDUCT OF BUTADIENE AND UNSATURATED DICARBOXYLIC ACID, NEUTRALIZER NIPPON OIL CO., LTD. (JP) 1979-11-20 US claimed
US-3952023-A Method for preparing adduct of butadiene polymer or copolymer and α, β-ethylenically unsaturated dicarboxylic acid compound NIPPON OIL COMPANY LTD. (JA) 1976-04-20 US claimed
JP-56011449-A None JP disclosed
JP-63303983-A None JP disclosed
US-3960957-A 2-(6'-methoxynaphth-2'yl) propionaldoxime and 5'-halo derivatives thereof SYNTEX CORPORATION (PM) 1976-06-01 US disclosed
US-3952023-A Method for preparing adduct of butadiene polymer or copolymer and α, β-ethylenically unsaturated dicarboxylic acid compound NIPPON OIL COMPANY LTD. (JA) 1976-04-20 US disclosed
US-3931224-A Aromatic imidodicarboxylic acid diallyl esters, prepolymers thereof, cured resins thereof, and processes for producing these TEIJIN LIMITED (JA) 1976-01-06 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-20140031552-A1 PROCESSES FOR PREPARING ISOINDOLINE-1,3-DIONE COMPOUNDS UGT1A1, CYP3A5, CYP3A7 TSHR 4230/4885CYP3A4 4/4885ESR1 4408/4885

“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.