Terephthalic Acid

Terephthalic Acid

SCHEMBL5969822

O=C(O)c1ccc(C(=O)O)cc1.[CsH]

nearest known ligand 0.92

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

OPRM1

The experimentally established mechanism targets of Terephthalic 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
▸ TSHR P16473 3/20 0.92
▸ TP53 P04637 1/20 0.92
▸ SRD5A2 P31213 4/20 0.75
▸ CA1 P00915 3/20 0.71
▸ CA2 P00918 3/20 0.71
▸ CA12 O43570 1/20 0.71
▸ CA3 P07451 1/20 0.71
▸ TYR P14679 1/20 0.71
▸ DRD1 P21728 1/20 0.71
▸ CA4 P22748 1/20 0.71
▸ CA6 P23280 1/20 0.71
▸ CA5A P35218 1/20 0.71
▸ CA7 P43166 1/20 0.71
▸ CA9 Q16790 1/20 0.71
▸ CA14 Q9ULX7 1/20 0.71
▸ CA5B Q9Y2D0 1/20 0.71
▸ NAPRT Q6XQN6 2/20 0.69
▸ DAO P14920 1/20 0.69
▸ ALDH1A1 P00352 2/20 0.67
▸ ALOX15 P16050 1/20 0.67

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
Terephthalic Acid SCHEMBL1655 0.96 TSHR (1.00) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL5053781 0.96 TSHR (1.00) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL2511919 0.96 TSHR (1.00) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL175823 0.96 TSHR (1.00) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL25381766 0.92 TSHR (0.92) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL156613 0.92 TSHR (0.92) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL1151273 0.92 TSHR (0.92) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL20704876 0.92 TSHR (0.92) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL21443891 0.92 TSHR (0.92) TSHRTP53SRD5A2CA1CA2
Terephthalic Acid SCHEMBL17667155 0.92 TSHR (0.92) TSHRTP53SRD5A2CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9704612-B2 Composition of silver-conjugated compound composite SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2017-07-11 — — US claimed
EP-2687304-B1 METAL COMPLEX COMPOSITIONS AND MIXTURE THEREOF SUMITOMO CHEMICAL CO (JP) 2019-01-23 — — EP disclosed
US-9704612-B2 Composition of silver-conjugated compound composite SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2017-07-11 — — US disclosed
EP-2687304-A1 METAL COMPLEX COMPOSITIONS AND MIXTURE THEREOF Sumitomo Chemical Company Limited (JP) 2014-01-22 — — EP disclosed
US-20140001422-A1 COMPOSITION OF SILVER-CONJUGATED COMPOUND COMPOSITE SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2014-01-02 — — US disclosed
US-20130341571-A1 METALLIC COMPOSITE COMPOSITION AND MIXTURE THEREOF SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2013-12-26 — — US disclosed
US-20060128608-A1 Novel chemical compounds and their use BIOTA SCIENTIFIC MANAGEMENT PTY LTD (AU) 2006-06-15 — — US disclosed
US-20030176610-A1 Poly(methylene/polyethylene terephthalate) copolymers BAYLOR UNIVERSITY 2003-09-18 — — US disclosed
US-6011133-A Laminates of glass or metal and poly(alkylene dicarboxylates) and syntheses thereof BAYLOR UNIVERSITY (US) 2000-01-04 — — US disclosed
US-5837381-A MULTILAYER PROTECTIVE COATING; WEAR AND CORROSION RESISTANCE UNIV BAYLOR (US) 1998-11-17 — — US disclosed
US-5668224-A TETRAALKYL- OR TRIALKYLAMMONIUM END GROUPS BAYLOR UNIVERSITY 1997-09-16 — — US disclosed
US-5451643-A PROTECTIVE COATINGS FOR METALS OR GLASS BAYLOR UNIVERSITY (US) 1995-09-19 — — US disclosed
WO-1994020296-A1 POLY (ALKYLENE DICARBOXYLATES) AND SYNTHESES THEREOF BAYLOR UNIVERSITY (US) 1994-09-15 — — WO 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-20060128608-A1 Novel chemical compounds and their use PGLS, ABCG2, UGCG TSHR 4534/4885TP53 2032/4885SRD5A2 2842/4885

“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.

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