SCHEMBL1241916

SCHEMBL1241916

CC(CC(=O)OCc1ccccc1)[C@H](N)C(=O)O

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC15A1 P46059 2/20 0.65
SLC1A3 P43003 3/20 0.53
SLC1A2 P43004 3/20 0.53
SLC1A1 P43005 3/20 0.53
KMT2A Q03164 2/20 0.53
MEN1 O00255 1/20 0.53
CYP1A2 P05177 1/20 0.53
CYP2D6 P10635 1/20 0.53
CYP2C9 P11712 1/20 0.53
CYP2C19 P33261 1/20 0.53
ALDH1A1 P00352 3/20 0.51
MAPK1 P28482 1/20 0.51
L3MBTL1 Q9Y468 1/20 0.51
MMP9 P14780 1/20 0.45
SLC6A2 P23975 1/20 0.44
SLC6A3 Q01959 1/20 0.44
TDP1 Q9NUW8 1/20 0.44
CDC25B P30305 1/20 0.43
ABCB1 P08183 1/20 0.42
CA12 O43570 1/20 0.42

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
SCHEMBL22804119 1.00 SLC15A1 (0.65) SLC15A1SLC1A3SLC1A2SLC1A1KMT2A
SCHEMBL28209173 0.88 SLC15A1 (0.60) SLC15A1SLC1A3SLC1A2SLC1A1KMT2A
SCHEMBL7385188 0.85 SLC15A1 (0.59) SLC15A1SLC1A3SLC1A2SLC1A1KMT2A
SCHEMBL84418 0.84 SLC15A1 (0.63) SLC15A1SLC1A3SLC1A2SLC1A1KMT2A
SCHEMBL6566591 0.84 SLC15A1 (0.63) SLC15A1SLC1A3SLC1A2SLC1A1KMT2A
SCHEMBL7207073 0.84 SLC15A1 (0.63) SLC15A1SLC1A3SLC1A2SLC1A1KMT2A
SCHEMBL27635124 0.83 SLC15A1 (0.59) SLC15A1SLC1A3SLC1A2SLC1A1KMT2A
SCHEMBL8447494 0.83 SLC15A1 (0.59) SLC15A1SLC1A3SLC1A2SLC1A1KMT2A
SCHEMBL9781868 0.83 SLC15A1 (0.59) SLC15A1SLC1A3SLC1A2SLC1A1KMT2A
SCHEMBL8323575 0.83 SLC15A1 (0.60) SLC15A1SLC1A3SLC1A2SLC1A1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109125260-A Amphipathic polymer is preparing the application in oral drugs 北京中医药大学 2019-01-04 CN claimed
WO-2025224463-A1 DESMURAMYLPEPTIDE ANALOGUE MONOESTER Imhotex Limited (GB) 2025-10-30 WO disclosed
WO-2025049064-A9 CARDIOPROTECTIVE LIPIDS AND METHODS OF USE SIGNPATH PHARMA INC. (US) 2025-05-22 WO disclosed
WO-2025049064-A2 CARDIOPROTECTIVE LIPIDS AND METHODS OF USE SIGNPATH PHARMA INC. (US) 2025-03-06 WO disclosed
CN-119522110-A Novel linker compounds and ligand-drug conjugates thereof 特里奥尔株式会社 2025-02-25 CN disclosed
CN-119451701-A Compounds comprising self-destructing groups and ligand-drug conjugates comprising the same 特里奥尔株式会社 2025-02-14 CN disclosed
EP-4472668-A1 PHOSPHORAMIDATE-BASED PSMA-TARGETED SMALL-MOLECULE DRUG CONJUGATES Cancer Targeted Technology LLC (US) 2024-12-11 EP disclosed
WO-2024224089-A1 DESMURAMYLPEPTIDE MONOESTERS AS NOD2 AGONISTS AND USE THEREOF Imhotex Limited (GB) 2024-10-31 WO disclosed
US-20240270765-A2 CARDIOPROTECTIVE LIPIDS AND METHODS OF USE SIGNPATH PHARMA INC. 2024-08-15 US disclosed
US-20240025928-A1 CARDIOPROTECTIVE LIPIDS AND METHODS OF USE SIGNPATH PHARMA INC (US) 2024-01-25 US disclosed
EP-0282891-B1 New thymopentin retro-inverso analogs and fragments thereof, a process of preparation of the new compounds and the intermediates obtained therein ENIRICERCHE SPA (IT) 1994-01-26 EP disclosed
EP-0565631-A1 ANTI-VIRAL COMPOUNDS. MERRELL DOW PHARMA (US) 1993-10-20 EP disclosed
WO-1993013066-A1 CYCLIC AMIDES OF 3-AMINO-2-HYDROXY-CARBOXYLIC ACIDS AS HIV-PROTEASE INHIBITORS SYNTEX (U.S.A.) INC. (US) 1993-07-08 WO disclosed
WO-1993005026-A1 PEPTIDE ISOTERS CONTAINING A HETEROCYCLE AS H.I.V. INHIBITORS SMITHKLINE BEECHAM CORPORATION (US) 1993-03-18 WO disclosed
WO-1992012123-A1 ANTI-VIRAL COMPOUNDS MERRELL DOW PHARMACEUTICALS INC. (US) 1992-07-23 WO disclosed
US-4880780-A RESPIRATORY SYSTEM DISORDERS ICI AMERICAS INC. (US) 1989-11-14 US disclosed
EP-0282891-A2 New thymopentin retro-inverso analogs and fragments thereof, a process of preparation of the new compounds and the intermediates obtained therein ENIRICERCHE S.p.A. (IT) 1988-09-21 EP disclosed
US-4369178-A Glucosamine peptide derivatives, their production and use TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1983-01-18 US disclosed
EP-0014984-A1 Glucosamine-peptide derivatives, their production and use Takeda Chemical Industries, Ltd. (JP) 1980-09-03 EP disclosed
US-4028315-A Solid phase synthesis of peptides E. R. SQUIBB & SONS, INC. (US) 1977-06-07 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-20240025928-A1 CARDIOPROTECTIVE LIPIDS AND METHODS OF USE CPT1B, FABP3, NR1H2 SLC15A1 2352/4885SLC1A3 2725/4885SLC1A2 2775/4885
US-20240270765-A2 CARDIOPROTECTIVE LIPIDS AND METHODS OF USE CPT1B, FABP3, NR1H2 SLC15A1 2352/4885SLC1A3 2725/4885SLC1A2 2775/4885

“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.