SCHEMBL1437012

SCHEMBL1437012

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

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MMP1 P03956 1/20 0.57
▸ MMP3 P08254 1/20 0.57
▸ MMP9 P14780 1/20 0.57
▸ MAPT P10636 6/20 0.56
▸ TDP1 Q9NUW8 4/20 0.56
▸ POLB P06746 3/20 0.56
▸ ALDH1A1 P00352 2/20 0.55
▸ THRB P10828 1/20 0.55
▸ CYP2C9 P11712 1/20 0.55
▸ CYP2C19 P33261 1/20 0.55
▸ HSD17B10 Q99714 1/20 0.55
▸ CTRB1 P17538 3/20 0.54
▸ ITGA4 P13612 1/20 0.54
▸ ITGB7 P26010 1/20 0.54
▸ CTSS P25774 2/20 0.53
▸ CTSL P07711 1/20 0.53
▸ CTSB P07858 1/20 0.53
▸ CTSK P43235 1/20 0.53
▸ NPSR1 Q6W5P4 3/20 0.53
▸ ATM Q13315 1/20 0.53

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
Hydrochloric Acid SCHEMBL27530934 0.99 MMP1 (0.56) MMP1MMP3MMP9MAPTTDP1
Hydrochloric Acid SCHEMBL5966853 0.99 MMP1 (0.56) MMP1MMP3MMP9MAPTTDP1
SCHEMBL31293473 0.90 MMP1 (0.55) MMP1MMP3MMP9MAPTTDP1
SCHEMBL15223643 0.88 ALDH1A1 (0.64) MMP1MMP3MMP9MAPTTDP1
SCHEMBL29484050 0.87 MMP1 (0.55) MMP1MMP3MMP9MAPTTDP1
SCHEMBL29973208 0.87 MMP1 (0.53) MMP1MMP3MMP9MAPTTDP1
SCHEMBL11786518 0.87 MMP1 (0.53) MMP1MMP3MMP9MAPTTDP1
SCHEMBL24346312 0.86 ALDH1A1 (0.72) POLBALDH1A1THRBCYP2C9CYP2C19
SCHEMBL5493329 0.86 ALDH1A1 (0.72) POLBALDH1A1THRBCYP2C9CYP2C19
SCHEMBL27336415 0.86 ALDH1A1 (0.72) POLBALDH1A1THRBCYP2C9CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
WO-2024225377-A1 METHOD FOR PRODUCING AMIDE GROUP-CONTAINING COMPOUND USING N-CARBOXYAMINO ACID ANHYDRIDE 中外製薬株式会社 2024-10-31 — — WO disclosed
US-20220017940-A1 FLUORESCENT PROBE FOR DETECTING CARBOXYPEPTIDASE ACTIVITY THE UNIVERSITY OF TOKYO (JP) 2022-01-20 — — US disclosed
US-20110053892-A1 Imidazo[4,5-d]Pyridazine Compounds For Treating Viral Infections LEIVERS MARTIN 2011-03-03 — — US disclosed
WO-2011026024-A2 IMIDAZO [4,5-D] PYRIDAZINE COMPOUNDS FOR TREATING VIRAL INFECTIONS GLAXOSMITHKLINE LLC (US) 2011-03-03 — — WO disclosed
US-20110052534-A1 Imidazopyridazine Compounds for Treating Viral Infections LEIVERS MARTIN 2011-03-03 — — US disclosed
WO-2011026091-A1 IMIDAZOPYRIDAZINE COMPOUNDS FOR TREATING VIRAL INFECTIONS GLAXOSMITHKLINE LLC (US) 2011-03-03 — — WO disclosed
US-7507764-B2 Amphiphilic [5:1]- and [3:3]- hexakisadducts of fullerenes TEGO BIOSCIENCES CORPORATION (US) 2009-03-24 — — US disclosed
US-20060223761-A1 Methods and compounds for inhibiting beta-amyloid peptide release and/or its synthesis ELAN PHARMACEUTICALS, INC. (US) 2006-10-05 — — US disclosed
US-20050143327-A1 Amphiphilic [5:1]- and [3:3]- hexakisadducts of fullerenes LUNA LABS USA, LLC 2005-06-30 — — US disclosed
US-20030229024-A1 Methods and compounds for inhibiting beta-amyloid peptide release and/or its synthesis AUDIA JAMES E (US) 2003-12-11 — — US disclosed
US-6476263-B1 Compounds for inhibiting β-amyloid peptide release and/or its synthesis ELAN PHARMACEUTICALS, INC. 2002-11-05 — — US disclosed
US-20020052322-A1 Methods and compounds for inhibiting beta-amyloid peptide release and/or its synthesis ELAN PHARMACEUTICALS, INC. 2002-05-02 — — US disclosed
US-6211235-B1 ALZHEIMERS DISEASE ELAN PHARMACEUTICALS, INC. 2001-04-03 — — US disclosed
US-6207710-B1 FOR THERAPY OF ALZHEIMER'S DISEASE ELAN PHARMACEUTICALS, INC. 2001-03-27 — — US disclosed
US-6191166-B1 ALZHEIMER'S DISEASE ELAN PHARMACEUTICALS, INC. 2001-02-20 — — US disclosed
EP-0942924-A2 METHODS AND COMPOUNDS FOR INHIBITING $g(b)-AMYLOID PEPTIDE RELEASE AND/OR ITS SYNTHESIS Elan Pharmaceuticals, Inc. (US) 1999-09-22 — — EP disclosed
WO-1998022494-A9 METHODS AND COMPOUNDS FOR INHIBITING β-AMYLOID PEPTIDE RELEASE AND/OR SYNTHESIS — 1998-08-20 — — WO disclosed
WO-1998022494-A2 METHODS AND COMPOUNDS FOR INHIBITING β-AMYLOID PEPTIDE RELEASE AND/OR SYNTHESIS ELAN PHARMACEUTICALS, INC. (US) 1998-05-28 — — WO disclosed
EP-0364804-A1 Non-peptide renin inhibitors ABBOTT LABORATORIES (US) 1990-04-25 — — 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 (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-20020052322-A1 Methods and compounds for inhibiting beta-amyloid peptide release and/or its synthesis APP, BACE1, IAPP MMP1 1115/4885MMP3 632/4885MMP9 535/4885
US-20110052534-A1 Imidazopyridazine Compounds for Treating Viral Infections ACE, ACE2, TPMT MMP1 1595/4885MMP3 2945/4885MMP9 3849/4885
US-20060223761-A1 Methods and compounds for inhibiting beta-amyloid peptide release and/or its synthesis APP, BACE1, IAPP MMP1 1277/4885MMP3 706/4885MMP9 572/4885
US-20030229024-A1 Methods and compounds for inhibiting beta-amyloid peptide release and/or its synthesis APP, BACE1, IAPP MMP1 1115/4885MMP3 632/4885MMP9 535/4885
US-20110053892-A1 Imidazo[4,5-d]Pyridazine Compounds For Treating Viral Infections MAVS, ZC3HAV1, IL5 MMP1 1974/4885MMP3 3431/4885MMP9 4364/4885

“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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