SCHEMBL392680

SCHEMBL392680

O=C(O)[C@H](Cc1ccccc1)N1C(=O)c2ccccc2C1=O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 1.00
GAA P10253 1/20 1.00
POLB P06746 4/20 0.82
AADAT Q8N5Z0 1/20 0.77
L3MBTL1 Q9Y468 2/20 0.77
TSHR P16473 1/20 0.74
KMT2A Q03164 4/20 0.70
PKM P14618 2/20 0.66
SMN1; SMN2 Q16637 3/20 0.65
MEN1 O00255 2/20 0.64
KDM4E B2RXH2 1/20 0.64
TP53 P04637 1/20 0.64
GLA P06280 1/20 0.64
CYP3A4 P08684 1/20 0.64
CYP2D6 P10635 1/20 0.64
HPGD P15428 1/20 0.64
ALOX12 P18054 1/20 0.64
NFKB1 P19838 1/20 0.64
APEX1 P27695 1/20 0.64
MAPK1 P28482 1/20 0.64

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
SCHEMBL4861809 1.00 ALDH1A1 (1.00) ALDH1A1GAAPOLBAADATL3MBTL1
SCHEMBL30216480 1.00 ALDH1A1 (1.00) ALDH1A1GAAPOLBAADATL3MBTL1
SCHEMBL478614 1.00 ALDH1A1 (1.00) ALDH1A1GAAPOLBAADATL3MBTL1
Hydrochloric Acid SCHEMBL7840775 0.98 ALDH1A1 (0.97) ALDH1A1GAAPOLBAADATL3MBTL1
SCHEMBL6692611 0.91 POLB (1.00) ALDH1A1GAAPOLBAADATL3MBTL1
SCHEMBL20246861 0.91 ALDH1A1 (0.82) ALDH1A1GAAPOLBAADATL3MBTL1
SCHEMBL8883949 0.91 ALDH1A1 (0.82) ALDH1A1GAAPOLBAADATL3MBTL1
SCHEMBL11463170 0.91 POLB (1.00) ALDH1A1GAAPOLBAADATL3MBTL1
SCHEMBL6635286 0.89 ALDH1A1 (0.80) ALDH1A1GAAPOLBAADATL3MBTL1
SCHEMBL10768539 0.89 ALDH1A1 (0.80) ALDH1A1GAAPOLBAADATL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114957384-B Synthesis method of dipeptide-4 湖北泓肽生物科技有限公司 2023-11-14 CN claimed
CN-114957384-A Synthesis method of dipeptide-4 湖北泓肽生物科技有限公司 2022-08-30 CN claimed
EP-0778827-B1 PROCESS FOR PRODUCING A BETA-AMINO ALCOHOL DEGUSSA (DE) 2001-12-12 EP claimed
US-5994555-A (4S,5S)-4-BENZYL-2-OXO-OXAZOLIDINE-5-CARBOXYLIC ACID FROM PHENYLALANINE AND PHTHALIC ANHYDRIDE F. HOFFMAN-LAROCHE AG (CH) 1999-11-30 US claimed
US-5859248-A Process for the production of a β-amino alcohol F. HOFFMAN-LA ROCHE AG (CH) 1999-01-12 US claimed
EP-0778827-A1 PROCESS FOR PRODUCING A BETA-AMINO ALCOHOL F. HOFFMANN-LA ROCHE AG (CH) 1997-06-18 EP claimed
WO-1996007642-A1 PROCESS FOR PRODUCING A β-AMINO ALCOHOL F. HOFFMANN-LA ROCHE AG (DE) 1996-03-14 WO claimed
EP-3924349-B1 AMINO ACID DERIVATIVES FOR THE TREATMENT OF INFLAMMATORY DISEASES THE ROSKAMP INST (US) 2025-06-25 EP disclosed
CN-114957384-B Synthesis method of dipeptide-4 湖北泓肽生物科技有限公司 2023-11-14 CN disclosed
CN-114957384-B Synthesis method of dipeptide-4 湖北泓肽生物科技有限公司 2023-11-14 CN disclosed
CN-114957384-A Synthesis method of dipeptide-4 湖北泓肽生物科技有限公司 2022-08-30 CN disclosed
CN-114957384-A Synthesis method of dipeptide-4 湖北泓肽生物科技有限公司 2022-08-30 CN disclosed
US-20220081415-A1 Amino Acid Derivatives for the Treatment of Inflammatory Diseases THE ROSKAMP INST (US) 2022-03-17 US disclosed
US-4613676-A PEPTIDES CIBA-GEIGY CORPORATION (US) 1986-09-23 US disclosed
EP-0143746-A2 5-Amino 4-hydroxy-valeryl-substituted derivatives CIBA-GEIGY AG (CH) 1985-06-05 EP disclosed
US-4329473-A HYPOTENSIVE AGENTS SRI INTERNATIONAL 1982-05-11 US disclosed
US-4242256-A Synthesis of peptide analogues SHARPE ROBERT (GB) 1980-12-30 US disclosed
US-4147700-A HYDRAZINOLYZING A PHTHALYL DERIVATIVE SHIONOGI & CO., LTD. (JP) 1979-04-03 US disclosed
US-4143048-A AMINATION SHIONOGI & CO., LTD. (JP) 1979-03-06 US disclosed
US-4141901-A REDUCING AN AZIDO DERIVATIVE SHIONOGI & CO., LTD. (JP) 1979-02-27 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 (1 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-20220081415-A1 Amino Acid Derivatives for the Treatment of Inflammatory Diseases NFKBIA, NFRKB, IKBKG ALDH1A1 4214/4885GAA 828/4885POLB 634/4885

“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.