Terephthalic Acid

Terephthalic Acid

SCHEMBL2187152

CC(=O)N(C)C.O=C(O)c1ccc(C(=O)O)cc1

nearest known ligand 0.63

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 0.63
TP53 P04637 1/20 0.63
ALDH1A1 P00352 3/20 0.56
SMN1; SMN2 Q16637 1/20 0.56
SRD5A2 P31213 3/20 0.55
CA1 P00915 3/20 0.52
CA2 P00918 3/20 0.52
CA12 O43570 1/20 0.52
CA3 P07451 1/20 0.52
TYR P14679 1/20 0.52
DRD1 P21728 1/20 0.52
CA4 P22748 1/20 0.52
CA6 P23280 1/20 0.52
CA5A P35218 1/20 0.52
CA7 P43166 1/20 0.52
CA9 Q16790 1/20 0.52
CA14 Q9ULX7 1/20 0.52
CA5B Q9Y2D0 1/20 0.52
POLB P06746 2/20 0.50
KMT2A Q03164 2/20 0.50

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
SCHEMBL28465550 0.87 MAPT (0.61) TSHRALDH1A1SMN1; SMN2SRD5A2DAO
Terephthalic Acid SCHEMBL9407875 0.86 TSHR (0.75) TSHRTP53ALDH1A1SMN1; SMN2SRD5A2
Terephthalic Acid SCHEMBL9407876 0.86 TSHR (0.75) TSHRTP53ALDH1A1SMN1; SMN2SRD5A2
Terephthalic Acid SCHEMBL8209798 0.83 TSHR (0.80) TSHRTP53ALDH1A1SMN1; SMN2SRD5A2
Terephthalic Acid SCHEMBL28358071 0.83 TSHR (0.80) TSHRTP53ALDH1A1SMN1; SMN2SRD5A2
Terephthalic Acid SCHEMBL123278 0.83 TSHR (0.80) TSHRTP53ALDH1A1SMN1; SMN2SRD5A2
SCHEMBL458926 0.82 ALDH1A1 (0.61) TSHRTP53ALDH1A1SMN1; SMN2SRD5A2
SCHEMBL8953838 0.81 POLB (0.53) TSHRTP53ALDH1A1SMN1; SMN2SRD5A2
Terephthalic Acid SCHEMBL8210119 0.80 TSHR (0.75) TSHRTP53ALDH1A1SMN1; SMN2SRD5A2
Terephthalic Acid SCHEMBL5706612 0.80 TSHR (0.75) TSHRTP53ALDH1A1SMN1; SMN2SRD5A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130261323-A1 INTEGRATED METHODS OF PREPARING RENEWABLE CHEMICALS GEVO, INC. (US) 2013-10-03 US disclosed
US-8450543-B2 Integrated methods of preparing renewable chemicals GEVO, INC. (US) 2013-05-28 US disclosed
US-20110172475-A1 INTEGRATED METHODS OF PREPARING RENEWABLE CHEMICALS GEVO, INC. (US) 2011-07-14 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 (2 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-20110172475-A1 INTEGRATED METHODS OF PREPARING RENEWABLE CHEMICALS ADH1A, ADH1C, FASN TSHR 4760/4885TP53 3397/4885ALDH1A1 95/4885
US-20130261323-A1 INTEGRATED METHODS OF PREPARING RENEWABLE CHEMICALS ADH1A, ADH1C, FASN TSHR 4760/4885TP53 3397/4885ALDH1A1 95/4885

“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.