SCHEMBL691707

SCHEMBL691707

O=Cc1ccc2cc(C(=O)O)ccc2c1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.63
UNG P13051 1/20 0.60
KDM4E B2RXH2 4/20 0.52
TRIM24 O15164 1/20 0.51
TRIM33 Q9UPN9 1/20 0.51
PTPN1 P18031 2/20 0.44
HPGD P15428 1/20 0.43
ENPP2 Q13822 1/20 0.43
HSD17B10 Q99714 1/20 0.43
KMT2A Q03164 2/20 0.42
MEN1 O00255 1/20 0.42
TP53 P04637 1/20 0.42
TSHR P16473 1/20 0.42
CYP1B1 Q16678 1/20 0.42
PTGS2 P35354 2/20 0.42
CA12 O43570 1/20 0.42
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42
POLB P06746 1/20 0.42
GAA P10253 1/20 0.42

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
SCHEMBL30196606 1.00 ALDH1A1 (0.63) ALDH1A1UNGKDM4ETRIM24TRIM33
SCHEMBL12213021 0.96 ALDH1A1 (0.59) ALDH1A1UNGKDM4ETRIM24TRIM33
SCHEMBL12213019 0.96 ALDH1A1 (0.59) ALDH1A1UNGKDM4ETRIM24TRIM33
SCHEMBL12213020 0.96 ALDH1A1 (0.59) ALDH1A1UNGKDM4ETRIM24TRIM33
SCHEMBL12213018 0.94 ALDH1A1 (0.61) ALDH1A1UNGKDM4ETRIM24TRIM33
Diethylamine SCHEMBL28167539 0.88 ALDH1A1 (0.50) ALDH1A1UNGKDM4ETRIM24TRIM33
Formic Acid SCHEMBL28281907 0.83 KDM4E (0.59) ALDH1A1UNGKDM4EPTPN1HPGD
SCHEMBL20024752 0.83 PARP10 (0.58) ALDH1A1UNGKDM4EKMT2APOLB
SCHEMBL18758 0.82 KDM4E (0.68) ALDH1A1KDM4EPTPN1HPGDENPP2
SCHEMBL29359975 0.82 KDM4E (0.68) ALDH1A1KDM4EPTPN1HPGDENPP2

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 1001 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120004721-A 2, 6-Naphthalene dicarboxylic acid product, preparation method thereof, acid precipitation method of 2, 6-naphthalene dicarboxylic acid and application thereof 中国石油化工股份有限公司 2025-05-16 CN claimed
CN-120004724-A Method for separating and purifying 2, 6-naphthalene dicarboxylic acid and purified 2, 6-naphthalene dicarboxylic acid 中国石油化工股份有限公司 2025-05-16 CN claimed
CN-120004723-A Method for synthesizing polymerization grade 2, 6-naphthalene dicarboxylic acid by using crude 2, 6-naphthalene dicarboxylic acid and polymerization grade 2, 6-naphthalene dicarboxylic acid 中国石油化工股份有限公司 2025-05-16 CN claimed
CN-118854692-A Self-repairing organic silicon synthetic leather and preparation method and application thereof 江西纳恩新材料有限公司 2024-10-29 CN claimed
CN-115215740-B Method for separating and purifying 2, 6-naphthalene dicarboxylic acid and obtained 2, 6-naphthalene dicarboxylic acid 中国石油化工股份有限公司 2024-06-28 CN claimed
CN-117917393-A Method for separating and purifying 2, 6-naphthalene dicarboxylic acid 中国石油化工股份有限公司 2024-04-23 CN claimed
CN-117843471-A Method for purifying 2, 6-naphthalene dicarboxylic acid 中国石油化工股份有限公司 2024-04-09 CN claimed
CN-114426480-B Hydrofining method of crude 2,6-naphthalene dicarboxylic acid 中国石油化工股份有限公司 2024-03-26 CN claimed
CN-115594574-A Composition and method for removing color from crude polysubstituted carboxyarene or the like containing colored impurities 中国石油化工股份有限公司(CN) 2023-01-13 CN claimed
CN-115215740-A Method for separating and purifying 2,6-naphthalenedicarboxylic acid and 2,6-naphthalenedicarboxylic acid obtained by same 中国石油化工股份有限公司 2022-10-21 CN claimed
WO-2006071028-A1 METHOD FOR PREPARING TRANSFORMANTS EXPRESSING BENZALDEHYDE DEHYDROGENASE AND PREPATION OF 2,6-NAPHTHALENE DICARBOXYLIC ACID USING THE TRANSFORMANTS HYOSUNG CORPORATION (KR) 2006-07-06 WO claimed
US-6755991-B2 ESPECIALLY 2,6-NAPHTHALENEDICARBOXYLIC ACID MIXED WITH 6-FORMYL-2-NAPHTHOIC ACID, 6-METHOXYCARBONYL-2-NAPHTHOIC ACID OR TRIMELLITIC ACID; ALKALI METAL COMPOUND KABUSHIKI KAISHA UENO SEIYAKU OYO KENKYUJO (JP) 2004-06-29 US claimed
US-6756509-B2 REDUCING CRUDE 2,6-NAPHTHALENEDICARBOXYLIC ACID CONTAINING 6-FORMYL-2-NAPHTHOIC ACID WITH HYDROGEN AND CLEANING THE REDUCTION PRODUCT WITH ALCOHOL. KOBE STEEL, LTD. (JP) 2004-06-29 US claimed
US-20030088121-A1 Method for purifying crude 2,6-naphthalenedicarboxylic acid KABUSHIKI KAISHA KOBE SEIKO SHO(KOBE STEEL, LTD.) (JP) 2003-05-08 US claimed
EP-1275634-A1 Method for purifying crude 2,6-Naphthalenedicarboxylic acid Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) (JP) 2003-01-15 EP claimed
US-20020045728-A1 Aromatic dicarboxylic acid composition and liquid crystalline polyester resin made from the same KABUSHIKI KAISHA UENO SEIYAKU OYO KENKYUJO 2002-04-18 US claimed
WO-2001096859-A1 THE RAPID EVALUATION METHOD OF HYDROPURIFICATION CATALYST SAMSUNG GENERAL CHEMICALS CO., LTD. (KR) 2001-12-20 WO claimed
US-6255525-B1 MIXING WITH SOLVENT IN THE PRESENCE OF HYDROGEN GAS WITH CARBON CATALYST FREE OF HYDROGENATION METAL COMPONENT AT ELEVATED TEMPERATURE AND PRESSURE BP AMOCO CORPORATION 2001-07-03 US claimed
WO-1999029652-A1 PROCESS FOR PREPARING PURIFIED CARBOXYLIC ACIDS BP AMOCO CORPORATION (US) 1999-06-17 WO claimed
US-5770764-A SALT FORMATION WITH DI- OR TRIALKYLAMINE AMOCO CORPORATION (US) 1998-06-23 US 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 (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-20030088121-A1 Method for purifying crude 2,6-naphthalenedicarboxylic acid ADH1C, DHCR24, ADH1A ALDH1A1 134/4885UNG 596/4885KDM4E 3205/4885

“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.