SCHEMBL4855282

SCHEMBL4855282

CCC(CC(=O)OC)NCc1ccccc1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.44
MEN1 O00255 2/20 0.44
POLB P06746 2/20 0.43
LMNA P02545 2/20 0.43
L3MBTL1 Q9Y468 2/20 0.42
ALDH1A1 P00352 2/20 0.42
MAPT P10636 1/20 0.42
PPID Q08752 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.41
TRPM8 Q7Z2W7 1/20 0.41
SIGMAR1 Q99720 1/20 0.41
KDM4E B2RXH2 2/20 0.41
CA1 P00915 2/20 0.41
CA2 P00918 2/20 0.41
HPGD P15428 1/20 0.41
CA12 O43570 1/20 0.40
CA3 P07451 1/20 0.40
CA4 P22748 1/20 0.40
CA6 P23280 1/20 0.40
CA5A P35218 1/20 0.40

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
SCHEMBL8996651 1.00 KMT2A (0.44) KMT2AMEN1POLBLMNAL3MBTL1
SCHEMBL8996549 1.00 KMT2A (0.44) KMT2AMEN1POLBLMNAL3MBTL1
SCHEMBL4408805 0.92 MEN1 (0.48) KMT2AMEN1POLBLMNAL3MBTL1
SCHEMBL4851565 0.88 PPID (0.54) KMT2AMEN1POLBLMNAL3MBTL1
SCHEMBL4857826 0.88 MEN1 (0.43) KMT2AMEN1POLBLMNAL3MBTL1
SCHEMBL4856050 0.88 SIGMAR1 (0.49) KMT2AMEN1L3MBTL1MAPTTRPM8
SCHEMBL4856075 0.88 MEN1 (0.44) KMT2AMEN1LMNAL3MBTL1ALDH1A1
SCHEMBL4855741 0.86 MEN1 (0.43) KMT2AMEN1LMNAL3MBTL1ALDH1A1
SCHEMBL17462362 0.86 CA1 (0.49) KMT2AMEN1LMNAL3MBTL1ALDH1A1
SCHEMBL4855726 0.85 POLB (0.46) KMT2AMEN1POLBLMNAL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12358932-B2 Chemical compounds BORAH, INC. (US) 2025-07-15 US disclosed
US-20240368196-A1 CHEMICAL COMPOUNDS BORAH, INC. 2024-11-07 US disclosed
EP-3994142-A1 CHEMICAL COMPOUNDS Borah, Inc. (US) 2022-05-11 EP disclosed
CN-114341145-A Chemical compound 博拉公司 2022-04-12 CN disclosed
WO-2021003501-A1 CHEMICAL COMPOUNDS Boragen, Inc. (US) 2021-01-07 WO disclosed
EP-1493819-B1 PROCESS FOR PRODUCING EITHER OPTICALLY ACTIVE N-SUBSTITUTED BETA-AMINO ACID AND OPTICALLY ACTIVE N-SUBSTITUTED BETA-AMINO ACID ESTER OR OPTICALLY ACTIVE N-SUBSTITUTED 2-HOMOPIPECOLIC ACID AND OPTICALLY ACTIVE N-SUBSTITUTED 2-HOMOPIPECOLIC ACID ESTER UBE INDUSTRIES (JP) 2014-11-12 EP disclosed
US-7879862-B2 Central nervous system disorders; psychological disorders; anxiolytic agents; irritable bowel syndrome; antidepressants SMITHKLINE BEECHAM (CORK) LIMITED (IE) 2011-02-01 US disclosed
US-7879862-B2 Central nervous system disorders; psychological disorders; anxiolytic agents; irritable bowel syndrome; antidepressants SMITHKLINE BEECHAM (CORK) LIMITED (IE) 2011-02-01 US disclosed
US-7449325-B2 Process for enzymatically producing either optically active N-substituted β-amino acids or esters thereof or optically active N-substituted 2-homopipecolic acids or esters thereof UBE INDUSTRIES, LTD. (JP) 2008-11-11 US disclosed
US-20080194589-A1 Pyrazolo[1,5-Alpha]Pyrimidinyl Derivatives Useful as Corticotropin-Releasing Factor (Crf) Receptor Antagonists NEUROCRINE BIOSCIENCES, INC. (US) 2008-08-14 US disclosed
US-20080194589-A1 Pyrazolo[1,5-Alpha]Pyrimidinyl Derivatives Useful as Corticotropin-Releasing Factor (Crf) Receptor Antagonists NEUROCRINE BIOSCIENCES, INC. (US) 2008-08-14 US disclosed
US-20050170473-A1 Process for producing either optically active n-substituted beta-amino acid and optically active n-substituted beta-amino acid ester or optically active n-substituted 2-homopipecolic acid and optically active n-substituted 2-homopipecolic acid ester UBE INDUSTRIES, LTD. (JP) 2005-08-04 US disclosed
EP-1493819-A1 PROCESS FOR PRODUCING EITHER OPTICALLY ACTIVE N-SUBSTITUTED BETA-AMINO ACID AND OPTICALLY ACTIVE N-SUBSTITUTED BETA-AMINO ACID ESTER OR OPTICALLY ACTIVE N-SUBSTITUTED 2-HOMOPIPECOLIC ACID AND OPTICALLY ACTIVE N-SUBSTITUTED 2-HOMOPIPECOLIC ACID ESTER Ube Industries, Ltd. (JP) 2005-01-05 EP disclosed
EP-0269043-B1 PROCESS FOR PREPARING 3 PENTENOIC ACID ESTERS FROM 2-PENTENOIC ACID ESTERS BASF Aktiengesellschaft (DE) 1991-08-21 EP disclosed
US-4845269-A Preparation of 3-pentenoates from 2-pentenoates BASF AKTIENGESELLSCHAFT (DE) 1989-07-04 US disclosed
EP-0269043-A2 Process for preparing 3 pentenoic acid esters from 2-pentenoic acid esters BASF Aktiengesellschaft (DE) 1988-06-01 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 (4 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-20050170473-A1 Process for producing either optically active n-substituted beta-amino acid and optically active n-substituted beta-amino acid ester or optically active n-substituted 2-homopipecolic acid and optically active n-substituted 2-homopipecolic acid ester CYP8B1, SRR, HM13 KMT2A 4504/4885MEN1 3529/4885POLB 2773/4885
US-20240368196-A1 CHEMICAL COMPOUNDS PDE4A, PDE4B, SYK KMT2A 1015/4885MEN1 2669/4885POLB 2931/4885
US-12358932-B2 Chemical compounds PDE4A, PDE4B, SYK KMT2A 1015/4885MEN1 2669/4885POLB 2931/4885
US-20080194589-A1 Pyrazolo[1,5-Alpha]Pyrimidinyl Derivatives Useful as Corticotropin-Releasing Factor (Crf) Receptor Antagonists CRHR1, CRH, CRHR2 KMT2A 4048/4885MEN1 1984/4885POLB 3949/4885

“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.