SCHEMBL667582

SCHEMBL667582

O=C(O)c1cc(-c2ccccc2)c(C(=O)O)cc1-c1ccccc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTPN1 P18031 4/20 0.59
FOLH1 Q04609 1/20 0.58
HNF4A P41235 3/20 0.57
AKR1C2 P52895 4/20 0.55
AKR1C1 Q04828 4/20 0.55
AKR1C3 P42330 2/20 0.55
ALDH1A1 P00352 1/20 0.55
ALOX15 P16050 1/20 0.55
PTPN6 P29350 2/20 0.53
PTPN2 P17706 1/20 0.53
ACMSD Q8TDX5 3/20 0.52
DHFR P00374 1/20 0.52
MCL1 Q07820 1/20 0.52
HSD17B10 Q99714 1/20 0.52
FABP3 P05413 1/20 0.52
FABP4 P15090 1/20 0.52
FABP5 Q01469 1/20 0.52
BACE1 P56817 1/20 0.50
BCAT2 O15382 1/20 0.50
PRKAB2 O43741 1/20 0.47

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
SCHEMBL28439181 0.95 PTPN1 (0.55) PTPN1FOLH1HNF4AAKR1C2AKR1C1
SCHEMBL5569233 0.95 PTPN1 (0.55) PTPN1FOLH1HNF4AAKR1C2AKR1C1
SCHEMBL9171492 0.93 PTPN1 (0.57) PTPN1FOLH1HNF4AAKR1C2AKR1C1
SCHEMBL7772423 0.90 PTPN1 (0.59) PTPN1FOLH1HNF4AAKR1C2AKR1C1
SCHEMBL5851553 0.88 PTPN1 (0.57) PTPN1FOLH1HNF4AAKR1C2AKR1C1
Hydrochloric Acid SCHEMBL8067582 0.87 HNF4A (0.55) PTPN1FOLH1HNF4AAKR1C2AKR1C1
SCHEMBL594177 0.87 IDO1 (0.57) PTPN1FOLH1HNF4AAKR1C2AKR1C1
SCHEMBL11356171 0.86 FOLH1 (0.47) PTPN1FOLH1HNF4AAKR1C2AKR1C1
SCHEMBL6500060 0.85 ALDH1A1 (0.51) PTPN1FOLH1HNF4AAKR1C2AKR1C1
SCHEMBL28486818 0.84 CYP2C8 (0.56) PTPN1FOLH1HNF4AAKR1C3ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12629654-B2 Concentration of chemical species through the use of photosenstive sorbent materials GENESIS SYSTEMS LLC (US) 2026-05-19 US claimed
US-20250197653-A1 MODULATING OBJECT SIGNATURES THROUGH THE USE OF PHOTOSENSTIVE SORBENT COATINGS GENESIS SYSTEMS LLC 2025-06-19 US claimed
US-20250196095-A1 CONCENTRATION OF CHEMICAL SPECIES THROUGH THE USE OF PHOTOSENSTIVE SORBENT MATERIALS GENESIS SYSTEMS LLC 2025-06-19 US claimed
CN-117720824-A Improved method for manufacturing quinacridone solid solution pigment 温州金源新材料科技有限公司 2024-03-19 CN claimed
EP-1890992-B1 AN ENRICHMENT PROCESS USING COMPOUNDS USEFUL IN A POLYESTER PROCESS GRUPO PETROTEMEX SA DE CV (MX) 2019-10-23 EP claimed
CN-105693536-B A kind of preparation method for synthesizing quinacridone pigment intermediate DXTA 温州永宏科技孵化有限公司 2017-12-01 CN claimed
US-7494641-B2 Extraction process for removal of impurities from an oxidizer purge stream in the synthesis of carboxylic acid EASTMAN CHEMICAL COMPANY (US) 2009-02-24 US claimed
EP-1890992-A2 AN ENRICHMENT PROCESS USING COMPOUNDS USEFUL IN A POLYESTER PROCESS EASTMAN CHEMICAL COMPANY (US) 2008-02-27 EP claimed
WO-2006125158-A2 AN ENRICHMENT PROCESS USING COMPOUNDS USEFUL IN A POLYESTER PROCESS EASTMAN CHEMICAL COMPANY (US) 2006-11-23 WO claimed
US-20060264656-A1 Enrichment process using compounds useful in a polyester process FUJITSU LIMITED (JP) 2006-11-23 US claimed
EP-0655052-A1 PROCESS FOR PREPARING 2,5-DIPHENYLTEREPHTHALIC ACID EASTMAN CHEMICAL COMPANY (US) 1995-05-31 EP claimed
US-5334754-A Process for preparing 2,5-diphenylterephthalic acid by oxidation EASTMAN CHEMICAL COMPANY (US) 1994-08-02 US claimed
WO-1994004481-A1 PROCESS FOR PREPARING 2,5-DIPHENYLTEREPHTHALIC ACID EASTMAN CHEMICAL COMPANY (US) 1994-03-03 WO claimed
US-12629654-B2 Concentration of chemical species through the use of photosenstive sorbent materials GENESIS SYSTEMS LLC (US) 2026-05-19 US disclosed
US-20250196095-A1 CONCENTRATION OF CHEMICAL SPECIES THROUGH THE USE OF PHOTOSENSTIVE SORBENT MATERIALS GENESIS SYSTEMS LLC 2025-06-19 US disclosed
US-20250197653-A1 MODULATING OBJECT SIGNATURES THROUGH THE USE OF PHOTOSENSTIVE SORBENT COATINGS GENESIS SYSTEMS LLC 2025-06-19 US disclosed
WO-1994004481-A1 PROCESS FOR PREPARING 2,5-DIPHENYLTEREPHTHALIC ACID EASTMAN CHEMICAL COMPANY (US) 1994-03-03 WO disclosed
US-4161607-A Thermally stable, rigid bisphenols E. I. DU PONT DE NEMOURS AND COMPANY (US) 1979-07-17 US disclosed
US-4065432-A Thermally stable, rigid polyesters from aromatic dibasic acids and thermally stable, rigid bisphenols E. I. DU PONT DE NEMOURS AND COMPANY (US) 1977-12-27 US disclosed
US-4065431-A Thermally stable, rigid polyesters from aromatic dibasic acids and thermally stable, rigid diols E. I. DU PONT DE NEMOURS AND COMPANY (US) 1977-12-27 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 (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-12629654-B2 Concentration of chemical species through the use of photosenstive sorbent materials TRPV4, TRPA1, TRPM4 PTPN1 3473/4885FOLH1 544/4885HNF4A 261/4885

“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.