SCHEMBL25347292

SCHEMBL25347292

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

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP10 Q53GL7 9/20 0.43
PARP4 Q9UKK3 2/20 0.43
CA1 P00915 2/20 0.43
CA2 P00918 2/20 0.43
PARP1 P09874 2/20 0.43
PARP2 Q9UGN5 1/20 0.43
PARP15 Q460N3 2/20 0.41
ALDH1A1 P00352 1/20 0.41
KMT2A Q03164 1/20 0.41
PARP14 Q460N5 1/20 0.41
PARP16 Q8N5Y8 1/20 0.41
PARP11 Q9NR21 1/20 0.41
GPR119 Q8TDV5 2/20 0.41
AAK1 Q2M2I8 1/20 0.38
ELANE P08246 1/20 0.38
NOS1 P29475 1/20 0.37
CA12 O43570 1/20 0.36
CA9 Q16790 1/20 0.36
CA14 Q9ULX7 1/20 0.36
POLB P06746 1/20 0.36

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
SCHEMBL3256088 0.84 MAPT (0.44) CA1CA2ALDH1A1KMT2AELANE
SCHEMBL29394739 0.84 RAB9A (0.39) CA1CA2ALDH1A1KMT2AELANE
Acetic Acid SCHEMBL6648493 0.83 NQO2 (0.44)
SCHEMBL6914487 0.82 CYP3A4 (0.39) CA1CA2ALDH1A1ELANECA12
SCHEMBL8385557 0.80 MAPT (0.39) PARP10CA1CA2PARP15ALDH1A1
SCHEMBL19998352 0.79 CYP3A4 (0.37) PARP10CA1CA2ALDH1A1GPR119
SCHEMBL5360319 0.79 MT-CO2 (0.37) CA1CA2ELANEMAPTMT-CO2
SCHEMBL5421359 0.79 RAB9A (0.43) ALDH1A1KMT2AAAK1MAPTTSHR
SCHEMBL8736767 0.78 MEN1 (0.43) ALDH1A1KMT2ACYP3A4TSHRCYP2C19
SCHEMBL6648429 0.77 POLB (0.44) ALDH1A1POLBMAPTTSHRHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12552739-B2 Method for preparing primary amide compounds from secondary or tertiary amides INDUSTRY FOUNDATION OF CHONNAM NATIONAL UNIVERSITY (KR) 2026-02-17 US disclosed
US-20230234913-A1 METHOD FOR PREPARING PRIMARY AMIDE COMPOUNDS FROM SECONDARY OR TERTIARY AMIDES INDUSTRY FOUNDATION OF CHONNAM NATIONAL UNIVERSITY (KR) 2023-07-27 US disclosed
US-20230234913-A1 METHOD FOR PREPARING PRIMARY AMIDE COMPOUNDS FROM SECONDARY OR TERTIARY AMIDES INDUSTRY FOUNDATION OF CHONNAM NATIONAL UNIVERSITY (KR) 2023-07-27 US disclosed
US-20230234913-A1 METHOD FOR PREPARING PRIMARY AMIDE COMPOUNDS FROM SECONDARY OR TERTIARY AMIDES INDUSTRY FOUNDATION OF CHONNAM NATIONAL UNIVERSITY (KR) 2023-07-27 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 (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-20230234913-A1 METHOD FOR PREPARING PRIMARY AMIDE COMPOUNDS FROM SECONDARY OR TERTIARY AMIDES CA3, NAAA, ATL3 PARP10 2269/4885PARP4 2845/4885CA1 11/4885
US-12552739-B2 Method for preparing primary amide compounds from secondary or tertiary amides CPS1, NAAA, MLN PARP10 3223/4885PARP4 3132/4885CA1 59/4885

“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.