Naphthoic Acid

Naphthoic Acid

SCHEMBL785728

Cl.O=C(O)c1cccc2ccccc12

nearest known ligand 0.95

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
HDAC8 known ✓ Q9BY41 1/20 0.59
HSP90AA1 known ✓ P07900 1/20 0.51
NR4A1 P22736 1/20 0.95
NR4A2 P43354 1/20 0.95
NR4A3 Q92570 1/20 0.95
CDC25B P30305 2/20 0.74
LDHA P00338 1/20 0.64
WDR5 P61964 1/20 0.61
PTPN1 P18031 2/20 0.60
MMP3 P08254 1/20 0.59
PLK1 P53350 1/20 0.57
ALDH1A1 P00352 4/20 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
HPGD P15428 2/20 0.51
HTT P42858 2/20 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 SCHEMBL27641446 1.00 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BLDHA
Naphthoic Acid SCHEMBL28110155 0.98 NR4A1 (1.00) NR4A1NR4A2NR4A3CDC25BLDHA
Naphthoic Acid SCHEMBL30233567 0.98 NR4A1 (1.00) NR4A1NR4A2NR4A3CDC25BLDHA
Naphthoic Acid SCHEMBL29352220 0.98 NR4A1 (1.00) NR4A1NR4A2NR4A3CDC25BLDHA
Naphthoic Acid SCHEMBL17258 0.98 NR4A1 (1.00) NR4A1NR4A2NR4A3CDC25BLDHA
Naphthoic Acid SCHEMBL6912565 0.95 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BLDHA
Naphthoic Acid SCHEMBL3823412 0.95 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BLDHA
Naphthoic Acid SCHEMBL1407017 0.95 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BLDHA
Naphthoic Acid SCHEMBL20591191 0.95 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BLDHA
Naphthoic Acid SCHEMBL9178942 0.95 NR4A1 (0.95) NR4A1NR4A2NR4A3CDC25BLDHA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4567210-A 4-ACYL-2-PHENYL-1-OXA-3,4-DIAZOL-5-ONES AS BLOWING AGENTS BAYER AKTIENGESELLSCHAFT (DE) 1986-01-28 US claimed
EP-0059596-B1 N-NAPHTHOYLGLYCINE DERIVATIVES AYERST, MCKENNA AND HARRISON INC. (CA) 1985-04-24 EP claimed
EP-0059596-A1 N-Naphthoylglycine derivatives AYERST, MCKENNA AND HARRISON INC. (CA) 1982-09-08 EP claimed
US-4331613-A Process for the preparation of trifluoromethylnaphthalenes BAYER AKTIENGESELLSCHAFT (DE) 1982-05-25 US claimed
US-4272502-A Process for preparing gaseous hydrogen chloride from dilute aqueous hydrochloric acid CHEMISCHE WERKE HULS AKTIENGESELLSCHAFT (DE) 1981-06-09 US claimed
JP-4099748-A None JP disclosed
JP-6009493-A None JP disclosed
JP-61134364-A None JP disclosed
EP-3512905-B1 METHOD FOR PRODUCING A POLYBENZAZOL POLYMER (P) BASF SE (DE) 2022-08-24 EP disclosed
US-11306053-B2 Ester compound and lubricating oil base oil DAISAN KASEI CO., LTD (JP) 2022-04-19 US disclosed
US-20210230096-A1 ESTER COMPOUND AND LUBRICATING OIL BASE OIL DAISAN KASEI CO., LTD (JP) 2021-07-29 US disclosed
EP-3512905-A1 METHOD FOR PRODUCING A POLYBENZAZOL POLYMER (P) BASF SE (DE) 2019-07-24 EP disclosed
US-4284584-A REACTING AN ANHYDRIDE WITH AN ALKALI METAL CYANIDE BAYER AKTIENGESELLSCHAFT (DE) 1981-08-18 US disclosed
US-4272502-A Process for preparing gaseous hydrogen chloride from dilute aqueous hydrochloric acid CHEMISCHE WERKE HULS AKTIENGESELLSCHAFT (DE) 1981-06-09 US disclosed
US-4265633-A Process for the manufacture of vat dyes CIBA-GEIGY AG (CH) 1981-05-05 US disclosed
US-4209462-A Method for preparing acyl cyanides STAUFFER CHEMICAL COMPANY (US) 1980-06-24 US disclosed
US-4143068-A PROCESS FOR THE PREPARATION OF ACYL CYANIDE COMPOUNDS BAYER AKTIENGESELLSCHAFT (DE) 1979-03-06 US disclosed
US-4069252-A Process for the preparation of certain acyl cyanide compounds BAYER AKTIENGESELLSCHAFT (DT) 1978-01-17 US disclosed
US-4018767-A 5-ENDO-(1-NAPHTHOYLOXY)-N-(AMINOALKYL) BICYCLO(2.2.1)HEPTANE-2,3-DI-ENDO-CARBOXYLIC ACID IMIDES BRISTOL-MYERS COMPANY (US) 1977-04-19 US disclosed
US-3980667-A Anti-arrhythmic 5-endo-substituted oxy-N-(aminoloweralkyl)bicycle [2.2.2.]oc BRISTOL-MYERS COMPANY (US) 1976-09-14 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 (2 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-11306053-B2 Ester compound and lubricating oil base oil F12, ELOVL1, HRH1 HDAC8 2456/4885HSP90AA1 685/4885NR4A1 1730/4885
US-20210230096-A1 ESTER COMPOUND AND LUBRICATING OIL BASE OIL F12, ELOVL1, HRH1 HDAC8 2456/4885HSP90AA1 685/4885NR4A1 1730/4885

“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.