SCHEMBL7274381

SCHEMBL7274381

CN[C@H](C(=O)OC)C(C)C

nearest known ligand 0.58

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CA14 Q9ULX7 4/20 0.58
CA12 O43570 3/20 0.58
SMN1; SMN2 Q16637 4/20 0.48
TSHR P16473 1/20 0.46
CA7 P43166 2/20 0.46
CA9 Q16790 2/20 0.46
TAS1R3 Q7RTX0 1/20 0.41
TAS1R1 Q7RTX1 1/20 0.41
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
CYP2C9 P11712 1/20 0.40
CYP2C19 P33261 1/20 0.40
MAPT P10636 1/20 0.39
HSD17B10 Q99714 1/20 0.39
GAA P10253 2/20 0.38
THRB P10828 1/20 0.37
BIRC2 Q13490 1/20 0.36
ALDH1A1 P00352 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
SCHEMBL6966533 1.00 CA14 (0.58) CA14CA12SMN1; SMN2TSHRCA7
SCHEMBL13204470 1.00 CA14 (0.58) CA14CA12SMN1; SMN2TSHRCA7
Hydrochloric Acid SCHEMBL17559741 0.97 CA14 (0.56) CA14CA12SMN1; SMN2TSHRCA7
Hydrochloric Acid SCHEMBL1761465 0.97 CA14 (0.56) CA14CA12SMN1; SMN2TSHRCA7
Hydrochloric Acid SCHEMBL29398016 0.97 CA14 (0.56) CA14CA12SMN1; SMN2TSHRCA7
SCHEMBL24445693 0.82 CA14 (0.45) CA14CA12SMN1; SMN2TSHRCA7
SCHEMBL8164724 0.82 CA14 (0.45) CA14CA12SMN1; SMN2TSHRCA7
SCHEMBL24556376 0.82 CA14 (0.45) CA14CA12SMN1; SMN2TSHRCA7
SCHEMBL10654071 0.82 CA12 (0.40) CA14CA12SMN1; SMN2TSHRCA7
SCHEMBL9925882 0.82 CA14 (0.45) CA14CA12SMN1; SMN2TSHRCA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12624053-B2 Ras inhibitors Revolution Medicines, Inc. (US) 2026-05-12 US disclosed
US-20260070930-A1 RAS INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT 2026-03-12 US disclosed
EP-4688790-A1 MACROCYCLIC RAS INHIBITORS Revolution Medicines, Inc. (US) 2026-02-11 EP disclosed
EP-4688789-A1 MACROCYCLIC RAS INHIBITORS Revolution Medicines, Inc. (US) 2026-02-11 EP disclosed
US-20260028353-A1 MACROCYCLIC RAS INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT 2026-01-29 US disclosed
US-20250388608-A1 RAS INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION, AS AGENT 2025-12-25 US disclosed
US-20250368661-A1 RAS INHIBITORS REVOLUTION MEDICINES INC (US) 2025-12-04 US disclosed
EP-4656201-A2 RAS INHIBITORS Revolution Medicines, Inc. (US) 2025-12-03 EP disclosed
US-12384790-B2 Pteridinone compounds and uses thereof VERTEX PHARMACEUTICALS INCORPORATED (US) 2025-08-12 US disclosed
US-20250195521-A1 USE OF SOS1 INHIBITORS TO TREAT MALIGNANCIES WITH SHP2 MUTATIONS Revolution Medicines, Inc. 2025-06-19 US disclosed
US-20170226124-A1 PHTHALAZINONE DERIVATIVES KUDOS PHARMACEUTICALS LIMITED (GB) 2017-08-10 US disclosed
US-20100234307-A1 PREPARATION AND USE OF BIPHENYL AMINO ACID DERIVATIVES FOR THE TREATMENT OF OBESITY BAYER HEALTHCARE LLC (US) 2010-09-16 US disclosed
US-20100016295-A1 Preparation and Use of Biphenyl Amino Acid Derivatives for the Treatment of Obesity BAYER HEALTHCARE LLC (US) 2010-01-21 US disclosed
CN-101583352-A Preparation and use of biphenyl amino acid derivatives for the treatment of obesity BAYER PHARMACEUTICALS CORP (US) 2009-11-18 CN disclosed
US-7553969-B1 Substituted phenethylamine derivatives CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2009-06-30 US disclosed
US-7553969-B1 Substituted phenethylamine derivatives CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2009-06-30 US disclosed
WO-2007049803-A1 NEW CYCLIC PEPTIDE COMPOUNDS ASTELLAS PHARMA INC. (JP) 2007-05-03 WO disclosed
WO-2004080976-A1 PHTHALAZINONE DERIVATIVES KUDOS PHARMACEUTICALS LIMITED (GB) 2004-09-23 WO disclosed
US-4668683-A Cardiotonic quinazoline derivatives KYOWA HAKKO KOGYO K.K. (JP) 1987-05-26 US disclosed
EP-0195667-A2 Cardiotonic quinazoline derivatives KYOWA HAKKO KOGYO KABUSHIKI KAISHA (JP) 1986-09-24 EP 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 (10 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-20250368661-A1 RAS INHIBITORS KRAS, NRAS, HRAS CA14 3948/4885CA12 4023/4885SMN1; SMN2 3728/4885
US-20260070930-A1 RAS INHIBITORS KRAS, NRAS, RIN1 CA14 4565/4885CA12 3608/4885SMN1; SMN2 4241/4885
US-20170226124-A1 PHTHALAZINONE DERIVATIVES NR0B1, NR0B2, NR2E1 CA14 2063/4885CA12 1947/4885SMN1; SMN2 3650/4885
US-20260028353-A1 MACROCYCLIC RAS INHIBITORS KRAS, NRAS, HRAS CA14 3262/4885CA12 3386/4885SMN1; SMN2 3943/4885
US-20250195521-A1 USE OF SOS1 INHIBITORS TO TREAT MALIGNANCIES WITH SHP2 MUTATIONS SOS1, PPM1D, PTPN1 CA14 4556/4885CA12 4480/4885SMN1; SMN2 986/4885
US-12624053-B2 Ras inhibitors KRAS, NRAS, HMGCR CA14 4511/4885CA12 4070/4885SMN1; SMN2 4495/4885
US-20250388608-A1 RAS INHIBITORS KRAS, NRAS, HMGCR CA14 4511/4885CA12 4070/4885SMN1; SMN2 4495/4885
US-20100016295-A1 Preparation and Use of Biphenyl Amino Acid Derivatives for the Treatment of Obesity BCAT2, BCAT1, FABP4 CA14 4718/4885CA12 4717/4885SMN1; SMN2 4427/4885
US-20100234307-A1 PREPARATION AND USE OF BIPHENYL AMINO ACID DERIVATIVES FOR THE TREATMENT OF OBESITY BCAT2, BCAT1, FABP4 CA14 4718/4885CA12 4717/4885SMN1; SMN2 4427/4885
US-12384790-B2 Pteridinone compounds and uses thereof DPYD, PKD1, TYMP CA14 4431/4885CA12 4350/4885SMN1; SMN2 1711/4885

“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.