Isophthalic Acid

Isophthalic Acid

SCHEMBL377398

Cl.Cl.O=C(O)c1cccc(C(=O)O)c1

nearest known ligand 0.80

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 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 1/20 0.68
CA12 O43570 1/20 0.68
CA1 P00915 1/20 0.68
CA6 P23280 1/20 0.68
CA9 Q16790 1/20 0.68
TSHR P16473 2/20 0.63
DAO P14920 1/20 0.63
NAPRT Q6XQN6 1/20 0.63
KMO O15229 1/20 0.62
CYP1A2 P05177 1/20 0.62
CYP2C9 P11712 1/20 0.62
HPGD P15428 1/20 0.62
HSD17B10 Q99714 1/20 0.62
UNG P13051 1/20 0.60
L3MBTL1 Q9Y468 2/20 0.59
ATM Q13315 1/20 0.59
TDP1 Q9NUW8 1/20 0.59
FOLH1 Q04609 1/20 0.58
AKR1C3 P42330 1/20 0.58
TP53 P04637 2/20 0.56

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 SCHEMBL9241794 1.00 CA12 (0.68) CA12CA1CA2CA6CA9
Isophthalic Acid SCHEMBL69359 1.00 CA12 (0.68) CA12CA1CA2CA6CA9
Isophthalic Acid SCHEMBL8084576 1.00 CA12 (0.68) CA12CA1CA2CA6CA9
Isophthalic Acid SCHEMBL5522892 1.00 CA12 (0.68) CA12CA1CA2CA6CA9
Isophthalic Acid SCHEMBL22462 0.97 CA12 (0.71) CA12CA1CA2CA6CA9
Isophthalic Acid SCHEMBL20500514 0.97 CA12 (0.71) CA12CA1CA2CA6CA9
Isophthalic Acid SCHEMBL28462260 0.97 CA12 (0.71) CA12CA1CA2CA6CA9
Isophthalic Acid SCHEMBL2512374 0.97 CA12 (0.71) CA12CA1CA2CA6CA9
Isophthalic Acid SCHEMBL147366 0.97 CA12 (0.71) CA12CA1CA2CA6CA9
Isophthalic Acid SCHEMBL28756611 0.97 CA12 (0.71) CA12CA1CA2CA6CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3758947-B1 HEAT SENSITIVE RECORDING MATERIAL AND COLOR DEVELOPER SOLENIS TECHNOLOGIES CAYMAN LP (KY) 2025-05-14 EP claimed
CN-115894899-A Polyamide copolymer PA5IT and preparation method thereof 上海凯赛生物技术股份有限公司 2023-04-04 CN claimed
CN-115894898-A Quaternary copolymerized polyamide PA56IT and preparation method thereof 上海凯赛生物技术股份有限公司 2023-04-04 CN claimed
CN-115894900-A Polyamide copolymer PA6IT and preparation method thereof 上海凯赛生物技术股份有限公司 2023-04-04 CN claimed
US-11512048-B2 Heat sensitive recording material, and color developer SOLENIS TECHNOLOGIES, L.P. (US) 2022-11-29 US claimed
CN-113637210-A Gas-barrier moisture-permeable film and preparation method and application thereof 中国石油化工股份有限公司 2021-11-12 CN claimed
CN-113634136-A Nanofiltration membrane and preparation method and application thereof 中国石油化工股份有限公司 2021-11-12 CN claimed
CN-110358081-B Preparation method of aromatic polyamide high polymer containing sulfonic group and having higher molecular weight 东华大学 2021-11-09 CN claimed
CN-113214472-A Low-water-absorption high-toughness polyamide copolymer 513TI and preparation method thereof 上海凯赛生物技术股份有限公司 2021-08-06 CN claimed
CN-113121817-A Polyamide copolymer 56TI with low water absorption rate, and preparation method and application thereof 上海凯赛生物技术股份有限公司 2021-07-16 CN claimed
EP-0040177-B1 PROCESS FOR THE PREPARATION OF BENZENE OR NAPHTHALENE ALKENYL CARBOXYLIC ACID DERIVATIVES CIBA-GEIGY AG (CH) 1983-07-20 EP claimed
EP-0025506-B1 POLYOXAZOLE PRECURSORS, THEIR PREPARATION AND THEIR USE SIEMENS AKTIENGESELLSCHAFT (DE) 1983-05-25 EP claimed
EP-0023662-B1 HEAT-RESISTENT POSITIVE PHOTORESISTS AND PROCESS FOR THE PREPARATION OF HEAT-RESISTENT RELIEF STRUCTURES SIEMENS AKTIENGESELLSCHAFT (DE) 1983-05-18 EP claimed
EP-0026821-B1 METHOD OF PRODUCING RELIEF STRUCTURES RESISTANT TO A HIGH TEMPERATURE, RELIEF STRUCTURES PRODUCED THEREBY AND THEIR USE SIEMENS AKTIENGESELLSCHAFT (DE) 1983-04-06 EP claimed
US-4335054-A Process for the preparation of alkenylbenzenecarboxylic acid derivatives and alkenylnaphthalenecarboxylic acid derivatives CIBA-GEIGY CORPORATION (US) 1982-06-15 US claimed
US-4335055-A Process for the preparation of alkenylbenzene derivatives or alkenylnaphthalene derivatives CIBA-GEIGY CORPORATION (US) 1982-06-15 US claimed
US-4278786-A BIS/P-AMINOPHENOL ETHER OF A BISPHENOL HITACHI, LTD. (JP) 1981-07-14 US claimed
US-4187364-A Crosslinkable polymers of unsaturated imides CIBA-GEIGY CORPORATION (US) 1980-02-05 US claimed
US-4100116-A AMINATION BAYER AKTIENGESELLSCHAFT (DE) 1978-07-11 US claimed
US-4091017-A FRIEDEL-CRAFTS CATALYSTS, HYDROLYSIS DYNAMIT NOBEL AKTIENGESELLSCHAFT (DT) 1978-05-23 US 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-11512048-B2 Heat sensitive recording material, and color developer SCN1A, NCS1, SCN5A CA2 394/4885CA12 775/4885CA1 55/4885

“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.