Sugi Predict

Sugi Predict / Compounds / SCHEMBL65502

SCHEMBL65502

SCHEMBL65502

CN(C(=O)OC(C)(C)C)[C@@H](Cc1ccccc1)C(=O)O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MMP13 P45452 1/20 0.46
▸ REN P00797 1/20 0.46
▸ ITGB3 P05106 1/20 0.45
▸ ITGA2B P08514 1/20 0.45
▸ ATM Q13315 1/20 0.44
▸ ITGA4 P13612 1/20 0.43
▸ ITGB7 P26010 1/20 0.43
▸ ACE P12821 1/20 0.43
▸ ALDH1A1 P00352 1/20 0.43
▸ MAPT P10636 1/20 0.43
▸ CTSS P25774 2/20 0.42
▸ ADAMTS5 Q9UNA0 1/20 0.42
▸ CTSL P07711 1/20 0.42
▸ CTSB P07858 1/20 0.42
▸ CTSK P43235 1/20 0.42
▸ CYP1A2 P05177 1/20 0.42
▸ SLC7A5 Q01650 1/20 0.42
▸ L3MBTL1 Q9Y468 1/20 0.41
▸ MMP2 P08253 1/20 0.41
▸ MMP9 P14780 1/20 0.41

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
SCHEMBL1401042 1.00 MMP13 (0.46) MMP13RENITGB3ITGA2BATM
SCHEMBL2476924 1.00 MMP13 (0.46) MMP13RENITGB3ITGA2BATM
SCHEMBL30688558 0.95 ITGB3 (0.45) MMP13RENITGB3ITGA2BATM
SCHEMBL22457743 0.95 ITGB3 (0.45) MMP13RENITGB3ITGA2BATM
SCHEMBL30688551 0.95 ITGB3 (0.45) MMP13RENITGB3ITGA2BATM
SCHEMBL18248052 0.92 ALDH1A1 (0.48) MMP13RENITGB3ITGA2BACE
SCHEMBL1401223 0.92 ALDH1A1 (0.48) MMP13RENITGB3ITGA2BACE
SCHEMBL28518117 0.92 ALDH1A1 (0.48) MMP13RENITGB3ITGA2BACE
SCHEMBL29624556 0.92 ALDH1A1 (0.48) MMP13RENITGB3ITGA2BACE
SCHEMBL8911125 0.92 ALDH1A1 (0.48) MMP13RENITGB3ITGA2BACE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118621394-A Pulse copper electroplating solution applied to circuit board 南雄市溢诚化工有限公司 2024-09-10 — — CN claimed
CN-118007135-A Corrosion inhibition method for inhibiting metal corrosion in sulfur-containing medium 福建理工大学 2024-05-10 — — CN claimed
EP-4685150-A1 METHOD FOR PRODUCING AMIDE GROUP-CONTAINING COMPOUND USING N-CARBOXYAMINO ACID ANHYDRIDE CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2026-01-28 — — EP disclosed
US-20260015313-A1 AMINO ACID ACTIVE ESTER AND SALT THEREOF PEPTIDREAM INC (JP) 2026-01-15 — — US disclosed
US-20250281424-A1 SMALL MOLECULE ANTAGONISTS OF PF4 ZHOU YUHANG (US) 2025-09-11 — — US disclosed
US-12331072-B2 Deprotection method and resin removal method in solid-phase reaction for peptide compound or amide compound, and method for producing peptide compound CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-06-17 — — US disclosed
US-20250188116-A1 DEPROTECTION METHOD AND RESIN REMOVAL METHOD IN SOLID-PHASE REACTION FOR PEPTIDE COMPOUND OR AMIDE COMPOUND, AND METHOD FOR PRODUCING PEPTIDE COMPOUND CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-06-12 — — US disclosed
EP-4534524-A1 AMINO ACID ACTIVE ESTER AND SALT THEREOF PeptiDream Inc. (JP) 2025-04-09 — — EP disclosed
CN-119708146-A Preparation method of cyclopeptide Lagunamide D 五邑大学 2025-03-28 — — CN disclosed
US-12240871-B2 Method for producing peptide compound NISSAN CHEMICAL CORPORATION (JP) 2025-03-04 — — US disclosed
US-20250037039-A1 MOLECULAR DATA STORAGE USING COST-FREE MOLECULAR LIBRARIES BROWN UNIVERSITY 2025-01-30 — — US disclosed
US-4603121-A ANALGESICS G. D. SEARLE & CO. (US) 1986-07-29 — — US disclosed
EP-0136720-A2 Enkephalin analogs G.D. Searle & Co. (US) 1985-04-10 — — EP disclosed
US-4510085-A Antihypertensive tetrapeptide amides G.D. SEARLE & CO. (US) 1985-04-09 — — US disclosed
US-4495178-A Enkephalin analogs G. D. SEARLE & CO. (US) 1985-01-22 — — US disclosed
US-4407746-A Cyclohexyl and phenyl substituted enkephalins G. D. SEARLE & CO. (US) 1983-10-04 — — US disclosed
EP-0081838-A1 Cyclohexyl and phenyl substituted enkephalins G.D. Searle & Co. (US) 1983-06-22 — — EP disclosed
US-4320051-A Analgesic tripeptide amides AMERICAN HOME PRODUCTS CORPORATION (US) 1982-03-16 — — US disclosed
US-4273704-A N-Adamantane-substituted tetrapeptide amides G. D. SEARLE & CO. (US) 1981-06-16 — — US disclosed
US-4178371-A ANALGESIC, NARCOTIC ANTAGONIST OR ANTIDIARRHEAL AGENT RECKITT & COLMAN PRODUCTS LIMITED (GB) 1979-12-11 — — 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 (5 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-12331072-B2 Deprotection method and resin removal method in solid-phase reaction for peptide compound or amide compound, and method for producing peptide compound VIP, PEPD, MLN MMP13 1319/4885REN 272/4885ITGB3 3392/4885
US-20260015313-A1 AMINO ACID ACTIVE ESTER AND SALT THEREOF NSUN3, BCAT1, SLC43A1 MMP13 2905/4885REN 503/4885ITGB3 2864/4885
US-20250281424-A1 SMALL MOLECULE ANTAGONISTS OF PF4 PF4, F12, F2 MMP13 3328/4885REN 2571/4885ITGB3 185/4885
US-12240871-B2 Method for producing peptide compound NGLY1, NPPA, NPEPPS MMP13 2428/4885REN 1579/4885ITGB3 3772/4885
US-20250188116-A1 DEPROTECTION METHOD AND RESIN REMOVAL METHOD IN SOLID-PHASE REACTION FOR PEPTIDE COMPOUND OR AMIDE COMPOUND, AND METHOD FOR PRODUCING PEPTIDE COMPOUND VIP, PEPD, MLN MMP13 1319/4885REN 272/4885ITGB3 3392/4885

“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.