Naphthoic Acid

Naphthoic Acid

SCHEMBL1407017

Br.O=C(O)c1cccc2ccccc12

nearest known ligand 0.95

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4

The experimentally established mechanism targets of Naphthoic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NR4A1 P22736 1/20 0.95
NR4A2 P43354 1/20 0.95
NR4A3 Q92570 1/20 0.95
CDC25B P30305 2/20 0.74
WDR5 P61964 1/20 0.61
PTPN1 P18031 2/20 0.60
LDHA P00338 1/20 0.59
MMP3 P08254 1/20 0.59
HDAC8 Q9BY41 1/20 0.59
PLK1 P53350 1/20 0.57
ALDH1A1 P00352 3/20 0.56
ALOX15 P16050 1/20 0.56
GFER P55789 1/20 0.54
KDM4E B2RXH2 1/20 0.53
HSD17B10 Q99714 1/20 0.52
MAPT P10636 2/20 0.51
HTT P42858 2/20 0.51
HSP90AA1 P07900 1/20 0.51
HPGD P15428 1/20 0.51
L3MBTL1 Q9Y468 2/20 0.50

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
Naphthoic Acid SCHEMBL29352220 0.98 NR4A1 (1.00) NR4A1NR4A2NR4A3CDC25BWDR5
Naphthoic Acid SCHEMBL28110155 0.98 NR4A1 (1.00) NR4A1NR4A2NR4A3CDC25BWDR5
Naphthoic Acid SCHEMBL30233567 0.98 NR4A1 (1.00) NR4A1NR4A2NR4A3CDC25BWDR5
Naphthoic Acid SCHEMBL17258 0.98 NR4A1 (1.00) NR4A1NR4A2NR4A3CDC25BWDR5
Naphthoic Acid SCHEMBL6912565 0.95 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BWDR5
Naphthoic Acid SCHEMBL785728 0.95 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BWDR5
Naphthoic Acid SCHEMBL3823412 0.95 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BWDR5
Naphthoic Acid SCHEMBL868482 0.95 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BWDR5
Naphthoic Acid SCHEMBL20591191 0.95 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BWDR5
Naphthoic Acid SCHEMBL9178942 0.95 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BWDR5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1923381-B1 Hydrogenation process for high-purity naphthalenedicarboxylic acid HYOSUNG CORP (KR) 2011-03-09 EP claimed
US-20080119666-A1 Hydrogenation process for high-purity naphthalenedicarboxylic acid HYOSUNG CORPORATION (KR) 2008-05-22 US claimed
EP-1923381-A1 Hydrogenation process for high-purity naphthalenedicarboxylic acid Hyosung Corporation (KR) 2008-05-21 EP claimed
WO-2016202894-A1 METHOD OF CONVERTING ALCOHOL TO HALIDE UNIVERSITAET DES SAARLANDES (DE) 2016-12-22 WO disclosed
CN-103833723-B The manufacture method of cyclic sulfonic acid ester and intermediate thereof 和光纯药工业株式会社 2016-08-17 CN disclosed
EP-2757102-B1 Intermediate for producing a cyclic sulfonic acid ester WAKO PURE CHEM IND LTD (JP) 2016-03-23 EP disclosed
US-8969591-B2 Method for producing cyclic sulfonic acid ester and intermediate thereof WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 2015-03-03 US disclosed
EP-2463281-B1 METHOD FOR PRODUCING CYCLIC SULFONIC ACID ESTER AND INTERMEDIATE THEREOF WAKO PURE CHEM IND LTD (JP) 2014-10-22 EP disclosed
EP-2757102-A1 1,3-propanesultone derivative useful in the preparation of a 1,3-propenesultone derivative Wako Pure Chemical Industries, Ltd. (JP) 2014-07-23 EP disclosed
CN-103833723-A METHOD FOR PRODUCING CYCLIC SULFONIC ACID ESTER AND INTERMEDIATE THEREOF WAKO PURE CHEM IND LTD 2014-06-04 CN disclosed
US-20140142324-A1 METHOD FOR PRODUCING CYCLIC SULFONIC ACID ESTER AND INTERMEDIATE THEREOF WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 2014-05-22 US disclosed
CN-101182292-B Hydrogenation process for high-purity naphthalenedicarboxylic acid HYOSUNG CORP. (KR) 2011-11-30 CN disclosed
EP-1923381-B1 Hydrogenation process for high-purity naphthalenedicarboxylic acid HYOSUNG CORP (KR) 2011-03-09 EP disclosed
JP-2008127383-A HYDROGENATION PROCESS FOR 2,6-NAPHTHALENEDICARBOXYLIC ACID HYOSUNG CORP 2008-06-05 JP disclosed
US-20080119666-A1 Hydrogenation process for high-purity naphthalenedicarboxylic acid HYOSUNG CORPORATION (KR) 2008-05-22 US disclosed
US-20080119666-A1 Hydrogenation process for high-purity naphthalenedicarboxylic acid HYOSUNG CORPORATION (KR) 2008-05-22 US disclosed
EP-1923381-A1 Hydrogenation process for high-purity naphthalenedicarboxylic acid Hyosung Corporation (KR) 2008-05-21 EP disclosed
EP-1923381-A1 Hydrogenation process for high-purity naphthalenedicarboxylic acid Hyosung Corporation (KR) 2008-05-21 EP disclosed
CN-101182292-A Hydrogenation process for high-purity naphthalenedicarboxylic acid HYOSUNG CORP (KR) 2008-05-21 CN disclosed
US-4044002-A ACYL BROMIDES AND A BROMINE SCAVENGER ELI LILLY AND COMPANY (US) 1977-08-23 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 (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-20140142324-A1 METHOD FOR PRODUCING CYCLIC SULFONIC ACID ESTER AND INTERMEDIATE THEREOF STS, TST, SULT1A1 NR4A1 2986/4885NR4A2 3589/4885NR4A3 3312/4885

“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.