Isophthalic Acid

Isophthalic Acid

SCHEMBL725833

O=C([O-])c1cccc(C(=O)O)c1.[Na+]

nearest known ligand 0.64

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 Isophthalic 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 3/20 0.62
CA4 known ✓ P22748 1/20 0.62
CA1 known ✓ P00915 2/20 0.56
CA12 known ✓ O43570 1/20 0.56
CA9 Q16790 2/20 0.56
CA6 P23280 1/20 0.56
KMO O15229 1/20 0.52
CYP1A2 P05177 1/20 0.52
CYP2C9 P11712 1/20 0.52
HPGD P15428 1/20 0.52
HSD17B10 Q99714 1/20 0.52
TP53 P04637 1/20 0.52
DAO P14920 1/20 0.50
TSHR P16473 1/20 0.50
NAPRT Q6XQN6 1/20 0.50
UNG P13051 1/20 0.50
FOLH1 Q04609 1/20 0.48
AKR1C3 P42330 1/20 0.48
L3MBTL1 Q9Y468 2/20 0.48
ATM Q13315 1/20 0.48

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
Isophthalic Acid SCHEMBL31187513 1.00 CA2 (0.62) CA2CA4CA1CA9CA12
Isophthalic Acid SCHEMBL15573521 0.96 CA2 (0.58) CA2CA4CA1CA9CA12
Isophthalic Acid SCHEMBL11436838 0.95 CA2 (0.56) CA2CA4CA1CA9CA12
Isophthalic Acid SCHEMBL6378446 0.95 CA2 (0.56) CA2CA4CA1CA9CA12
Isophthalic Acid SCHEMBL9930191 0.93 CA2 (0.54) CA2CA4CA1CA9CA12
Isophthalic Acid SCHEMBL15571521 0.93 CA2 (0.54) CA2CA4CA1CA9CA12
Isophthalic Acid SCHEMBL15571213 0.93 CA2 (0.54) CA2CA4CA1CA9CA12
Isophthalic Acid SCHEMBL1396770 0.92 CA2 (0.54) CA2CA4CA1CA9CA12
Isophthalic Acid SCHEMBL15572660 0.91 CA2 (0.52) CA2CA4CA1CA9CA12
Isophthalic Acid SCHEMBL6280491 0.91 CA2 (0.60) CA2CA4CA1CA9CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12630710-B1 1,5-pentanediol-based polyester compositions with enhanced crystallization rates and methods of manufacture THE BOARD OF REGENTS OF THE UNIVERSITY OF OKLAHOMA (US) 2026-05-19 US claimed
CN-117181077-A Smokeless sulfur-free firework whistle agent mixing device and method 万载县建坤化工有限公司 2023-12-08 CN claimed
CN-110981653-B Smokeless and sulfur-free firework flute sound agent and preparation method thereof 北京理工大学 2020-12-01 CN claimed
CN-110981653-A Smokeless and sulfur-free firework flute sound agent and preparation method thereof 北京理工大学 2020-04-10 CN claimed
US-8716404-B1 Polyesters modified by a combination of ionomer and fatty acid salts E I DU PONT DE NEMOURS AND COMPANY (US) 2014-05-06 US claimed
US-8609770-B2 Polyesters modified by a combination of ionomer and organic acid salts E I DU PONT DE NEMOURS AND COMPANY (US) 2013-12-17 US claimed
EP-2235108-B1 POLYESTERS MODIFIED BY A COMBINATION OF IONOMER AND ORGANIC ACID SALTS DU PONT (US) 2013-02-27 EP claimed
EP-2235107-B1 TOUGHENED POLY(TRIMETHYLENE TEREPHTHALATE) COMPOSITION WITH REDUCED MELT VISCOSITY DU PONT (US) 2012-09-26 EP claimed
US-8242209-B2 Renewable polyester and carboxylic acid salt as nucleator; moldings; improved stiffness and impact strength E I DU PONT DE NEMOURS AND COMPANY (US) 2012-08-14 US claimed
JP-4694094-B2 2011-06-01 JP claimed
US-20090192268-A1 POLYESTERS MODIFIED BY A COMBINATION OF IONOMER AND ORGANIC ACID SALTS E. I. DU PONT DE NEMOURS AND COMPANY (US) 2009-07-30 US claimed
US-20090192266-A1 TOUGHENED POLY(TRIMETHYLENE TEREPHTHALATE) COMPOSITION WITH REDUCED MELT VISCOSITY E.I DU PONT DE NEMOURS AND COMPANY (US) 2009-07-30 US claimed
WO-2009094362-A1 TOUGHENED POLY(TRIMETHYLENE TEREPHTHALATE) COMPOSITION WITH REDUCED MELT VISCOSITY E. I. DU PONT DE NEMOURS AND COMPANY (US) 2009-07-30 WO claimed
EP-1339781-B1 METHOD TO PRODUCE A POLY(TRIMETHYLENE TEREPHTHALATE) FILM DU PONT (US) 2008-12-31 EP claimed
US-6818160-B2 Nucleating polypropylene terephthalate prior to film formation by adding monosodium salt of aromatic dicarboxylic acid during resin synthesis, and controlling quench temperature during casting of film; reduce brittleness of the film on thermal aging E. I. DU PONT DE NEMOURS AND COMPANY 2004-11-16 US claimed
JP-2004522814-A 2004-07-29 JP claimed
EP-1339781-A1 METHOD TO PRODUCE A POLY(TRIMETHYLENE TEREPHTHALATE) FILM E.I. DUPONT DE NEMOURS AND COMPANY (US) 2003-09-03 EP claimed
EP-1114095-B1 NUCLEATING AGENT FOR POLYESTERS DU PONT (US) 2003-06-04 EP claimed
US-20020117081-A1 Method to improve properties of poly (Trimethylene terephthalate) film E. I. DU PONT DE NEMOURS AND COMPANY 2002-08-29 US claimed
WO-2002040583-A1 METHOD TO PRODUCE A POLY(TRIMETHYLENE TEREPHTHALATE) FILM E.I. DU PONT DE NEMOURS AND COMPANY (US) 2002-05-23 WO 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-12630710-B1 1,5-pentanediol-based polyester compositions with enhanced crystallization rates and methods of manufacture GRIN2D, SMCHD1, GRIN2C CA2 55/4885CA4 416/4885CA1 14/4885

“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.