SCHEMBL377175

SCHEMBL377175

O=C(O)C[C@H](C(=O)O)c1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.61
ALDH1A1 P00352 2/20 0.61
GAA P10253 1/20 0.61
POLB P06746 2/20 0.59
TDP1 Q9NUW8 1/20 0.59
CYP2C19 P33261 2/20 0.57
GABBR2 O75899 1/20 0.53
GABBR1 Q9UBS5 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.53
CYP1A2 P05177 1/20 0.51
TSHR P16473 1/20 0.51
CYP2D6 P10635 1/20 0.50
SRC P12931 1/20 0.50
MEN1 O00255 1/20 0.49
KMT2A Q03164 1/20 0.49
CPA1 P15085 2/20 0.48
CPB1 P15086 1/20 0.48
CPA3 P15088 1/20 0.48
CPB2 Q96IY4 1/20 0.48
LMNA P02545 2/20 0.48

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
SCHEMBL29903902 1.00 L3MBTL1 (0.61) L3MBTL1ALDH1A1GAAPOLBTDP1
SCHEMBL146867 1.00 L3MBTL1 (0.61) L3MBTL1ALDH1A1GAAPOLBTDP1
SCHEMBL377609 1.00 L3MBTL1 (0.61) L3MBTL1ALDH1A1GAAPOLBTDP1
SCHEMBL23782080 0.98 L3MBTL1 (0.59) L3MBTL1ALDH1A1GAAPOLBTDP1
SCHEMBL6739142 0.98 L3MBTL1 (0.59) L3MBTL1ALDH1A1GAAPOLBTDP1
SCHEMBL11137284 0.91 L3MBTL1 (0.71) L3MBTL1ALDH1A1GAAPOLBTDP1
SCHEMBL3274728 0.89 ALDH1A1 (0.51) L3MBTL1ALDH1A1GAAPOLBTDP1
SCHEMBL28306756 0.88 L3MBTL1 (0.59) L3MBTL1ALDH1A1GAAPOLBTDP1
SCHEMBL10717750 0.87 MEN1 (0.54) L3MBTL1ALDH1A1GAAPOLBTDP1
SCHEMBL9736992 0.86 GABBR2 (0.53) L3MBTL1ALDH1A1GAAPOLBTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117105931-A Method for preparing pyridopyrimidine compounds and intermediate thereof 上海翰森生物医药科技有限公司 2023-11-24 CN claimed
CN-108884081-B Process for separating enantiomers of piperazine derivatives 阿森纽荣股份公司 2022-11-01 CN claimed
EP-3419974-B1 PROCESS FOR THE SEPARATION OF ENANTIOMERS OF PIPERAZINE DERIVATIVES ASCENEURON SA (CH) 2021-05-05 EP claimed
US-10344021-B2 Process for the separation of enantiomers of piperazine derivatives ASCENEURON S A (CH) 2019-07-09 US claimed
EP-3419974-A1 PROCESS FOR THE SEPARATION OF ENANTIOMERS OF PIPERAZINE DERIVATIVES Asceneuron SA (CH) 2019-01-02 EP claimed
CN-108884081-A The method for separating the enantiomer of bridged piperazine derivatives 阿森纽荣股份公司 2018-11-23 CN claimed
WO-2017144635-A1 PROCESS FOR THE SEPARATION OF ENANTIOMERS OF PIPERAZINE DERIVATIVES ASCENEURON S. A. (CH) 2017-08-31 WO claimed
US-20070270487-A1 Novel process and intermediates 085 ASTRAZENECA AB (SE) 2007-11-22 US claimed
US-20250368642-A1 SYNTHESIS OF KEY INTERMEDIATE OF KRAS G12C INHIBITOR COMPOUND AMGEN INC. (US) 2025-12-04 US disclosed
US-20250368643-A1 SYNTHESIS OF KEY INTERMEDIATE OF KRAS G12C INHIBITOR COMPOUND AMGEN INC. (US) 2025-12-04 US disclosed
US-12398130-B2 Acid addition salts of piperazine derivatives ASCENEURON SA (CH) 2025-08-26 US disclosed
US-12391691-B2 Synthesis of key intermediate of KRAS G12C inhibitor compound AMGEN INC. (US) 2025-08-19 US disclosed
US-12391689-B2 Synthesis of key intermediate of KRAS G12C inhibitor compound AMGEN INC. (US) 2025-08-19 US disclosed
US-20250206735-A1 SYNTHESIS OF KEY INTERMEDIATE OF KRAS G12C INHIBITOR COMPOUND AMGEN INC. (US) 2025-06-26 US disclosed
WO-2006032023-A2 4-((PHENOXYALKYL)THIO)-PHENOXYACETIC ACIDS AND ANALOGS JANSSEN PHARMACEUTICA N.V. (BE) 2006-03-23 WO disclosed
US-20060058393-A1 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs JANSSEN PHARMACEUTICA N.V. (BE) 2006-03-16 US disclosed
US-20050124698-A1 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs CYMABAY THERAPEUTICS, INC. 2005-06-09 US disclosed
WO-2005042478-A2 4-((PHENOXYALKYL)THIO)-PHENOXYACETIC ACIDS AND ANALOGS JANSSEN PHARMACEUTICA, N.V. (BE) 2005-05-12 WO disclosed
WO-1995007260-A1 TETRAHYDROISOQUINOLINES AS ALPHA-2 ANTAGONISTS AND BIOGENIC AMINE UPTAKE INHIBITORS ABBOTT LABORATORIES (US) 1995-03-16 WO disclosed
US-5389638-A Nervous system disorders ABBOTT LABORATORIES (US) 1995-02-14 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 (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-10344021-B2 Process for the separation of enantiomers of piperazine derivatives CYP3A5, CYP4Z1, HTR5A L3MBTL1 4798/4885ALDH1A1 115/4885GAA 1712/4885
US-20060058393-A1 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs PPARA, PPARG, PPARD L3MBTL1 3198/4885ALDH1A1 1360/4885GAA 833/4885
US-20070270487-A1 Novel process and intermediates 085 CYP3A5, AGPAT5, CYP4F8 L3MBTL1 4414/4885ALDH1A1 377/4885GAA 961/4885
US-12391691-B2 Synthesis of key intermediate of KRAS G12C inhibitor compound KRAS, NRAS, HRAS L3MBTL1 3019/4885ALDH1A1 3493/4885GAA 2623/4885
US-20050124698-A1 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs PPARA, PPARG, PPARD L3MBTL1 3157/4885ALDH1A1 1558/4885GAA 803/4885
US-20250368643-A1 SYNTHESIS OF KEY INTERMEDIATE OF KRAS G12C INHIBITOR COMPOUND KRAS, NRAS, HRAS L3MBTL1 3019/4885ALDH1A1 3493/4885GAA 2623/4885
US-20250368642-A1 SYNTHESIS OF KEY INTERMEDIATE OF KRAS G12C INHIBITOR COMPOUND KRAS, NRAS, HRAS L3MBTL1 3019/4885ALDH1A1 3493/4885GAA 2623/4885
US-20250206735-A1 SYNTHESIS OF KEY INTERMEDIATE OF KRAS G12C INHIBITOR COMPOUND KRAS, NRAS, HRAS L3MBTL1 3019/4885ALDH1A1 3493/4885GAA 2623/4885
US-12398130-B2 Acid addition salts of piperazine derivatives DNPEP, GAA, SLC30A5 L3MBTL1 4743/4885ALDH1A1 63/4885GAA 2/4885
US-12391689-B2 Synthesis of key intermediate of KRAS G12C inhibitor compound KRAS, NRAS, HRAS L3MBTL1 3019/4885ALDH1A1 3493/4885GAA 2623/4885

“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.