Phthalic Acid

Phthalic Acid

SCHEMBL5159685

O=C(O)c1ccccc1C(=O)O.[Na+].[OH-]

nearest known ligand 0.88

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
CA12 known ✓ O43570 1/20 0.62
CA1 known ✓ P00915 1/20 0.62
CA2 known ✓ P00918 1/20 0.62
CA4 known ✓ P22748 1/20 0.62
ALDH1A1 P00352 4/20 0.88
ALOX15 P16050 1/20 0.88
AKR1C3 P42330 3/20 0.64
NAPRT Q6XQN6 2/20 0.62
KDM4E B2RXH2 1/20 0.62
HMGB1 P09429 1/20 0.62
HPGD P15428 1/20 0.62
CA6 P23280 1/20 0.62
CA7 P43166 1/20 0.62
SMN1; SMN2 Q16637 1/20 0.62
CA9 Q16790 1/20 0.62
CA14 Q9ULX7 1/20 0.62
MAPT P10636 2/20 0.59
HDAC8 Q9BY41 1/20 0.59
POLB P06746 1/20 0.56
NR4A1 P22736 3/20 0.54

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 SCHEMBL4584474 0.97 ALDH1A1 (0.82) ALDH1A1ALOX15AKR1C3NAPRTKDM4E
Phthalic Acid SCHEMBL4584478 0.97 ALDH1A1 (0.82) ALDH1A1ALOX15AKR1C3NAPRTKDM4E
Phthalic Acid SCHEMBL4168570 0.94 ALDH1A1 (0.78) ALDH1A1ALOX15AKR1C3NAPRTKDM4E
Phthalic Acid SCHEMBL28258532 0.94 ALDH1A1 (0.88) ALDH1A1ALOX15AKR1C3NAPRTKDM4E
Phthalic Acid SCHEMBL589206 0.94 ALDH1A1 (0.88) ALDH1A1ALOX15AKR1C3NAPRTKDM4E
Phthalic Acid SCHEMBL195822 0.94 ALDH1A1 (0.88) ALDH1A1ALOX15AKR1C3NAPRTKDM4E
Phthalic Acid SCHEMBL5668586 0.94 ALDH1A1 (1.00) ALDH1A1ALOX15AKR1C3NAPRTKDM4E
Phthalic Acid SCHEMBL10477086 0.94 ALDH1A1 (1.00) ALDH1A1ALOX15AKR1C3NAPRTKDM4E
Phthalic Acid SCHEMBL1332278 0.94 ALDH1A1 (1.00) ALDH1A1ALOX15AKR1C3NAPRTKDM4E
Phthalic Acid SCHEMBL146125 0.94 ALDH1A1 (1.00) ALDH1A1ALOX15AKR1C3NAPRTKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111019933-A Immobilized laccase, preparation method and application in antibiotic degradation 天津大学 2020-04-17 CN claimed
US-5104794-A Deconjugation of conjugated bilirubins to be measured using high performance liquid chromatography UNITIKA LTD. (JP) 1992-04-14 US claimed
US-20230414617-A1 PHARMACEUTICAL COMPOSITION COMPRISING ACID-BASE NEUTRALIZATION COMBINATION AND APPLICATION THEREOF CHENGDU KUACHANGAOPU MEDICAL TECH CO LTD (CN) 2023-12-28 US disclosed
EP-4223313-A1 PHARMACEUTICAL COMPOSITION COMPRISING ACID-BASE NEUTRALIZATION COMBINATION AND APPLICATION THEREOF Chengdu Kuachangaopu Medical Technology Co., Ltd. (CN) 2023-08-09 EP disclosed
CN-111809068-B Preparation method of ammonium metavanadate for all-vanadium redox flow battery 中国科学院过程工程研究所 2020-12-15 CN disclosed
CN-111809068-A Preparation method of ammonium metavanadate for all-vanadium redox flow battery 中国科学院过程工程研究所 2020-10-23 CN disclosed
CN-111019933-A Immobilized laccase, preparation method and application in antibiotic degradation 天津大学 2020-04-17 CN disclosed
CN-107722103-A A kind of extracting method of margosine 江苏金太阳纺织科技股份有限公司 2018-02-23 CN disclosed
EP-0678580-B1 Reagent for measuring direct bilirubin UNITIKA LTD (JP) 2007-02-21 EP disclosed
EP-1188770-A1 SUBSTANCE BINDING TO THE SUBSTRATE OF ACTIVATED BLOOD COAGULATION FACTOR IN COMPETITION WITH THIS FACTORTO THEREBY REGULATE THE R EACTION BETWEEN THE ACTIVATED BLOOD COAGULATION FACTOR AND THE SUBSTRATE, A PROCESS FOR PRODUCING THE SUBSTANCE AND BLOOD COAGULATION FACTOR-ADSORBENT WITH THE USE OF THE FUJIMORI KOGYO CO., LTD. (JP) 2002-03-20 EP disclosed
EP-0387784-B1 Quantitative determination of bilirubin and a reagent therefor UNITIKA LTD (JP) 1997-09-10 EP disclosed
US-5599661-A REAGENT COMPRISES BUFFER, TETRAPYRROLE COMPOUND, BILIRUBIN OXIDIZING COMPOUND OF BILIRUBIN OXIDASE, AN OXIDIZING AGENT, OR A DIAZONIUM SALT UNITIKA, LTD. (JP) 1997-02-04 US disclosed
EP-0678580-A2 Reagent for measuring direct bilirubin UNITIKA LTD. (JP) 1995-10-25 EP disclosed
US-5104794-A Deconjugation of conjugated bilirubins to be measured using high performance liquid chromatography UNITIKA LTD. (JP) 1992-04-14 US disclosed
EP-0387784-A2 Quantitative determination of bilirubin and a reagent therefor UNITIKA LTD. (JP) 1990-09-19 EP disclosed