Benzodiazepine

Benzodiazepine

SCHEMBL4144041

C1=Cc2ccccc2NN=C1.[C]

nearest known ligand 0.43

Full drug profile on Sugi Atlas →

Predicted protein targets (top 2)

geneUniProtsupporting neighboursconfidence
GAA P10253 1/20 0.43
MAPT P10636 1/20 0.43

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
Benzodiazepine SCHEMBL7160172 0.98 GAA (0.44) GAAMAPT
Benzodiazepine SCHEMBL8137 0.98 GAA (0.44) GAAMAPT
Benzodiazepine SCHEMBL6618830 0.96 GAA (0.43) GAAMAPT
Benzodiazepine SCHEMBL4420872 0.96 GAA (0.43) GAAMAPT
Benzodiazepine SCHEMBL936208 0.96 GAA (0.43) GAAMAPT
Benzodiazepine SCHEMBL11809777 0.96 GAA (0.43) GAAMAPT
Benzodiazepine SCHEMBL11484022 0.96 GAA (0.43) GAAMAPT
Benzodiazepine SCHEMBL11474576 0.96 GAA (0.43) GAAMAPT
Benzodiazepine SCHEMBL4700331 0.96 GAA (0.43) GAAMAPT
Benzodiazepine SCHEMBL8139617 0.96 GAA (0.43) GAAMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090062256-A1 LACTAMS SUBSTITUTED BY CYCLIC SUCCINATES AS INHIBITORS OF Abeta PROTEIN PRODUCTION BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2009-03-05 US disclosed
US-7456278-B2 Lactams substituted by cyclic succinates as inhibitors of Aβ protein production BRISTOL-MYERS SQUIBB PHARMA CORPORATION (US) 2008-11-25 US disclosed
US-20080103128-A1 LACTAMS SUBSTITUTED BY CYCLIC SUCCINATES AS INHIBITORS OF ABETTA PROTEIN PRODUCTION BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2008-05-01 US disclosed
US-7354914-B2 Lactams substituted by cyclic succinates as inhibitors of Aβ protein production BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2008-04-08 US disclosed
US-20050261274-A1 Lactams substituted by cyclic succinates as inhibitors of Abeta protein production OLSON RICHARD E 2005-11-24 US disclosed
EP-1593683-A2 Dihydro-2,3-Benzodiazepine derivatives ELI LILLY AND COMPANY (US) 2005-11-09 EP disclosed
US-6958329-B2 Lactams substituted by cyclic succinates as inhibitors of A-β protein production BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2005-10-25 US disclosed
EP-1157992-B1 Dihydro-2,3-Benzodiazepine derivatives LILLY CO ELI (US) 2005-08-24 EP disclosed
EP-0699678-B1 Crystalline form of dihydro-2,3-benzodiazepine derivative LILLY CO ELI (US) 2004-03-24 EP disclosed
US-20030119815-A1 Lactams substituted by cyclic succinates as inhibitors of A-beta protein production OLSON RICHARD E (US) 2003-06-26 US disclosed
US-5795886-A ANTICONVULSANTS ELI LILLY AND COMPANY (US) 1998-08-18 US disclosed
US-5665878-A Stereoselective process for producing dihydro-2,3-benzodiazepine derivatives ELI LILLY AND COMPANY (US) 1997-09-09 US disclosed
EP-0771198-A4 1997-05-28 EP disclosed
EP-0771198-A1 DIHYDRO-2,3-BENZODIAZEPINE DERIVATIVES ELI LILLY AND COMPANY (US) 1997-05-07 EP disclosed
CN-1128264-A Crystalline form of dihydro-2,3-benzodiazepine derivative LILLY CO ELI (US) 1996-08-07 CN disclosed
CN-1123282-A Stereoselective process for producing dihydro-2,3-benzodiazepine derivatives LILLY CO ELI (US) 1996-05-29 CN disclosed
CN-1122338-A Physical form of dihydro-2,3-benzodiazepine derivative LILLY CO ELI (US) 1996-05-15 CN disclosed
WO-1996006606-A1 DIHYDRO-2,3-BENZODIAZEPINE DERIVATIVES ELI LILLY AND COMPANY (US) 1996-03-07 WO disclosed
EP-0699677-A1 Stereoselective process for producing dihydro-2,3-benzodiazepine derivatives ELI LILLY AND COMPANY (US) 1996-03-06 EP disclosed
EP-0699676-A1 Physical form of dihidro-2,3-benzodiazepine derivative ELI LILLY AND COMPANY (US) 1996-03-06 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 (4 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-20050261274-A1 Lactams substituted by cyclic succinates as inhibitors of Abeta protein production BACE1, APP, APH1A GAA 253/4885MAPT 47/4885
US-20090062256-A1 LACTAMS SUBSTITUTED BY CYCLIC SUCCINATES AS INHIBITORS OF Abeta PROTEIN PRODUCTION BACE1, APP, APH1A GAA 253/4885MAPT 47/4885
US-20080103128-A1 LACTAMS SUBSTITUTED BY CYCLIC SUCCINATES AS INHIBITORS OF ABETTA PROTEIN PRODUCTION APH1A, APH1B, APP GAA 115/4885MAPT 105/4885
US-20030119815-A1 Lactams substituted by cyclic succinates as inhibitors of A-beta protein production APH1A, APH1B, APP GAA 98/4885MAPT 63/4885

“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.