SCHEMBL910423

SCHEMBL910423

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

nearest known ligand 0.70

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
▸ FOLH1 Q04609 6/20 0.70
▸ MME P08473 1/20 0.64
▸ ECE1 P42892 1/20 0.64
▸ NAALAD2 Q9Y3Q0 1/20 0.61
▸ PPARA Q07869 2/20 0.57
▸ PPARG P37231 1/20 0.57
▸ SIRT2 Q8IXJ6 1/20 0.56
▸ SIRT1 Q96EB6 1/20 0.56
▸ CASP1 P29466 1/20 0.55

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
Benzene SCHEMBL28226069 1.00 FOLH1 (0.70) FOLH1MMEECE1NAALAD2PPARA
SCHEMBL910232 1.00 FOLH1 (0.70) FOLH1MMEECE1NAALAD2PPARA
SCHEMBL910233 1.00 FOLH1 (0.70) FOLH1MMEECE1NAALAD2PPARA
Cyclopropane SCHEMBL5691187 0.96 FOLH1 (0.65) FOLH1MMEECE1NAALAD2PPARA
SCHEMBL24238520 0.95 FOLH1 (0.64) FOLH1MMEECE1NAALAD2PPARA
SCHEMBL9697060 0.95 FOLH1 (0.64) FOLH1MMEECE1NAALAD2PPARA
SCHEMBL19925534 0.95 FOLH1 (0.64) FOLH1MMEECE1NAALAD2PPARA
SCHEMBL19307785 0.95 FOLH1 (0.64) FOLH1MMEECE1NAALAD2PPARA
SCHEMBL9697579 0.95 MME (0.65) FOLH1MMEECE1NAALAD2CASP1
SCHEMBL9698236 0.95 FOLH1 (0.64) FOLH1MMEECE1NAALAD2PPARA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116642980-A Method for preparing microcystin imprinting material by plasma polymerization and application 临沂大学 2023-08-25 — — CN claimed
CN-112557572-B Method for detecting isomer content in Cbz-Glu 成都普康生物科技有限公司 2023-05-05 — — CN claimed
CN-108290919-B Azithromycin derivatives having epithelial barrier enhancing properties 艾比恩多制药有限责任公司 2022-06-17 — — CN claimed
US-10723752-B2 Azithromycin derivatives with epithelial barrier enhancement properties EPIENDO PHARMACEUTICALS EHF (IS) 2020-07-28 — — US claimed
US-20180354981-A1 Azithromycin Derivatives With Epithelial Barrier Enhancement Properties EPI-ENDO PHARMACEUTICALS EHF (IS) 2018-12-13 — — US claimed
EP-0550899-B1 Process for preparing derivatives of (R) 5-pentylamino-5-oxopentanoic acid with anticholecystokinin activity ROTTA RESEARCH LAB (IT) 1995-12-06 — — EP claimed
EP-0498830-B1 GLUTAMIC AND ASPARTIC ACID DERIVATIVES WITH ANTIGASTRIN ACTIVITY AND A METHOD FOR THEIR PREPARATION ROTTA RESEARCH LAB (IT) 1994-12-14 — — EP claimed
EP-0561863-B1 AMIDIC DERIVATIVES OF GLUTAMIC, ASPARTIC AND 2-AMINO ADIPIC ACIDS WITH ANTIGASTRIN ACTIVITY ROTTA RESEARCH LAB (IT) 1994-11-02 — — EP claimed
EP-0561863-A1 AMIDIC DERIVATIVES OF GLUTAMIC, ASPARTIC AND 2-AMINO ADIPIC ACIDS WITH ANTIGASTRIN ACTIVITY. ROTTA RESEARCH LAB (IT) 1993-09-29 — — EP claimed
EP-0550899-A1 Process for preparing derivatives of (R) 5-pentylamino-5-oxopentanoic acid with anticholecystokinin activity ROTTA RESEARCH LABORATORIUM S.P.A. (IT) 1993-07-14 — — EP claimed
EP-0498830-A1 GLUTAMIC AND ASPARTIC ACID DERIVATIVES WITH ANTIGASTRIN ACTIVITY AND A METHOD FOR THEIR PREPARATION. ROTTA RESEARCH LAB (IT) 1992-08-19 — — EP claimed
US-5130474-A For treatment of gastrointestinal disorders such as colitis, pancreatitis, antispastic agents and biliary diskinesia ROTTA RESEARCH LABORATORIUM SPA (IT) 1992-07-14 — — US claimed
WO-1992010479-A1 AMIDIC DERIVATIVES OF GLUTAMIC, ASPARTIC AND 2-AMINO ADIPIC ACIDS WITH ANTIGASTRIN ACTIVITY ROTTA RESEARCH LABORATORIUM S.P.A. (IT) 1992-06-25 — — WO claimed
WO-1991006529-A1 GLUTAMIC AND ASPARTIC ACID DERIVATIVES WITH ANTIGASTRIN ACTIVITY AND A METHOD FOR THEIR PREPARATION ROTTA RESEARCH LABORATORIUM S.P.A. (IT) 1991-05-16 — — WO claimed
EP-0344184-A1 DERIVATIVES OF (R) 5-PENTYLAMINO-5-OXOPENTANOIC ACID WITH ANTICHOLECYSTOKININ ACTIVITY. ROTTA RESEARCH LAB (IT) 1989-12-06 — — EP claimed
WO-1988005774-A1 DERIVATIVES OF (R) 5-PENTYLAMINO-5-OXOPENTANOIC ACID WITH ANTICHOLECYSTOKININ ACTIVITY ROTTA RESEARCH LABORATORIUM S.P.A. (IT) 1988-08-11 — — WO claimed
US-20260021190-A1 GLUCOSE-RESPONSIVE INSULIN CONJUGATES COMPRISING A PENTA-VALENT SUGAR CLUSTER FOR TREATMENT OF DIABETES MERCK SHARP & DOHME LLC (US) 2026-01-22 — — US disclosed
EP-4615487-A1 GLUCOSE-RESPONSIVE INSULIN CONJUGATES COMPRISING A PENTA-VALENT SUGAR CLUSTER FOR TREATMENT OF DIABETES Merck Sharp & Dohme LLC (US) 2025-09-17 — — EP disclosed
US-4678800-A INHIBITORS OF ANGIOTENSIN-CONVERTING ENZYME CIBA-GEIGY CORPORATION (US) 1987-07-07 — — US disclosed
EP-0191989-A1 Antibiotic isoxazole derivatives, their production and use Takeda Chemical Industries, Ltd. (JP) 1986-08-27 — — 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 (3 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-20260021190-A1 GLUCOSE-RESPONSIVE INSULIN CONJUGATES COMPRISING A PENTA-VALENT SUGAR CLUSTER FOR TREATMENT OF DIABETES INSR, GPR119, GLP1R FOLH1 368/4885MME 449/4885ECE1 2437/4885
US-20180354981-A1 Azithromycin Derivatives With Epithelial Barrier Enhancement Properties CFTR, AQP1, CTSA FOLH1 3638/4885MME 587/4885ECE1 120/4885
US-10723752-B2 Azithromycin derivatives with epithelial barrier enhancement properties CFTR, AQP1, CTSA FOLH1 3638/4885MME 587/4885ECE1 120/4885

“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.

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