Phthalic Acid

Phthalic Acid

SCHEMBL7897478

Cl.O=C([O-])c1ccccc1C(=O)[O-].[K+].[K+]

nearest known ligand 0.61

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 Phthalic 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
CA2 known ✓ P00918 2/20 0.48
HDAC8 known ✓ Q9BY41 1/20 0.39
ALDH1A1 P00352 6/20 0.61
KDM4E B2RXH2 4/20 0.61
HPGD P15428 3/20 0.61
CA4 P22748 2/20 0.48
ALOX15 P16050 2/20 0.48
NFKB1 P19838 1/20 0.42
MAPK1 P28482 1/20 0.42
CYP2C19 P33261 1/20 0.42
BLM P54132 1/20 0.42
CES2 O00748 2/20 0.40
CES1 P23141 2/20 0.40
CA12 O43570 1/20 0.40
CA1 P00915 1/20 0.40
HMGB1 P09429 1/20 0.40
CA6 P23280 1/20 0.40
CA7 P43166 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
CA9 Q16790 1/20 0.40

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
Phthalic Acid SCHEMBL10891143 1.00 ALDH1A1 (0.61) ALDH1A1KDM4EHPGDCA2CA4
Phthalic Acid SCHEMBL7875648 0.97 ALDH1A1 (0.58) ALDH1A1KDM4EHPGDCA2CA4
Phthalic Acid SCHEMBL109123 0.97 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDCA2CA4
Phthalic Acid SCHEMBL30001010 0.97 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDCA2CA4
Phthalic Acid SCHEMBL3914680 0.97 ALDH1A1 (0.64) ALDH1A1KDM4EHPGDCA2CA4
Phthalic Acid SCHEMBL11216044 0.94 ALDH1A1 (0.61) ALDH1A1KDM4EHPGDCA2CA4
Phthalic Acid SCHEMBL183233 0.94 ALDH1A1 (0.61) ALDH1A1KDM4EHPGDCA2CA4
Phthalic Acid SCHEMBL21494484 0.94 ALDH1A1 (0.61) ALDH1A1KDM4EHPGDCA2CA4
Phthalic Acid SCHEMBL120006 0.94 ALDH1A1 (0.61) ALDH1A1KDM4EHPGDCA2CA4
Phthalic Acid SCHEMBL486782 0.94 ALDH1A1 (0.61) ALDH1A1KDM4EHPGDCA2CA4

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5654156-A PREPARING REAGENT COMPRISING LIPOSOMES CONTAINING ANTIGEN OR ANTIBODY WHICH BINDS ANALYTE TO BE MEASURED, ENCAPSULATING MARKER THEREIN, ACIDIFYING SAMPLE, CONTACTING SAMPLE WITH REAGENT, MEASURING AMOUNT OF DETECTABLE MARKER RELEASED WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 1997-08-05 US claimed
JP-10215875-A None JP disclosed
US-6180839-B1 PREVENTING THE FORMATION OF A LIQUID TWO-PHASE MIXTURE IN THE REACTION MIXTURE; CONTROLLING THE AMOUNTS OF PRODUCT BY KEEPING THE RESIDENCE TIME CONCENTRATION COEFFICIENT IN A RANGE VALUE BASF AKTIENGESELLSCHAFT (DE) 2001-01-30 US disclosed
EP-0552954-B1 Immunoassay and reagents used therefor WAKO PURE CHEM IND LTD (JP) 1998-11-25 EP disclosed
JP-H10215875-A PURIFICATION OF PROTEIN MITSUBISHI CHEM CORP 1998-08-18 JP disclosed
US-5654156-A PREPARING REAGENT COMPRISING LIPOSOMES CONTAINING ANTIGEN OR ANTIBODY WHICH BINDS ANALYTE TO BE MEASURED, ENCAPSULATING MARKER THEREIN, ACIDIFYING SAMPLE, CONTACTING SAMPLE WITH REAGENT, MEASURING AMOUNT OF DETECTABLE MARKER RELEASED WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 1997-08-05 US disclosed
EP-0552954-A1 Immunoassay and reagents used therefor WAKO PURE CHEMICAL INDUSTRIES LTD (JP) 1993-07-28 EP disclosed
US-5116734-A Precipitation of the oxidized substrate complexed with a transition metal and a colloidal Group 1B metal compound; immunoassay DIGENE DIAGNOSTICS, INC. (US) 1992-05-26 US disclosed
WO-1991003718-A1 A HIGHLY SENSITIVE METHOD FOR DETECTING PEROXIDASE DIGENE DIAGNOSTICS, INC. (US) 1991-03-21 WO disclosed