Tolazamide

Tolazamide

SCHEMBL992662

CCCCNC(=O)NS(=O)(=O)c1ccc(C)cc1.Cc1ccc(S(=O)(=O)NC(=O)NN2CCCCCC2)cc1

nearest known ligand 0.75

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC8KCNJ11

The experimentally established mechanism targets of Tolazamide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.75
LMNA P02545 4/20 0.75
CYP2C9 P11712 2/20 0.75
TSHR P16473 2/20 0.75
CYP3A4 P08684 2/20 0.75
NFKB1 P19838 2/20 0.75
ALB P02768 1/20 0.75
TDP1 Q9NUW8 1/20 0.75
KDM4E B2RXH2 1/20 0.75
TP53 P04637 1/20 0.75
GLA P06280 1/20 0.75
GAA P10253 1/20 0.75
MAPT P10636 1/20 0.75
ALOX12 P18054 1/20 0.75
FBP1 P09467 3/20 0.56
AKR1C3 P42330 1/20 0.53
CA12 O43570 1/20 0.49
CA1 P00915 1/20 0.49
CA2 P00918 1/20 0.49
CA9 Q16790 1/20 0.49

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
Tolazamide SCHEMBL747962 0.93 ALDH1A1 (0.65) ALDH1A1LMNACYP2C9TSHRCYP3A4
Tolazamide SCHEMBL2534564 0.88 ALDH1A1 (0.70) ALDH1A1LMNACYP2C9TSHRCYP3A4
Tolazamide SCHEMBL13725632 0.87 ALDH1A1 (1.00) ALDH1A1LMNACYP2C9TSHRCYP3A4
Tolbutamide SCHEMBL15918 0.87 ALDH1A1 (1.00) ALDH1A1LMNACYP2C9TSHRCYP3A4
Tolazamide SCHEMBL34417 0.87 ALDH1A1 (1.00) ALDH1A1LMNACYP2C9TSHRCYP3A4
Tolbutamide SCHEMBL1536920 0.87 ALDH1A1 (1.00) ALDH1A1LMNACYP2C9TSHRCYP3A4
Glypinamide SCHEMBL5243890 0.86 ALDH1A1 (0.59) ALDH1A1LMNACYP2C9TSHRCYP3A4
Tolbutamide SCHEMBL140363 0.85 ALDH1A1 (0.97) ALDH1A1LMNACYP2C9TSHRCYP3A4
Tolbutamide SCHEMBL11357518 0.85 ALDH1A1 (0.97) ALDH1A1LMNACYP2C9TSHRCYP3A4
Tolbutamide SCHEMBL11356450 0.85 ALDH1A1 (0.97) ALDH1A1LMNACYP2C9TSHRCYP3A4

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-3458033-B1 TRIPLE DRUG COMBINATION (METFORMIN, SIMVASTATIN, DIGOXIN) FOR TARGETED TREATMENT OF PANCREATIC CANCER UNIV CALIFORNIA (US) 2023-07-05 EP disclosed
US-11197844-B2 Triple drug combination (metformin, simvastatin, digoxin) for targeted treatment of pancreatic cancer THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2021-12-14 US disclosed
US-20210100770-A1 TRIPLE DRUG COMBINATION (METFORMIN, SIMVASTATIN, DIGOXIN) FOR TARGETED TREATMENT OF PANCREATIC CANCER THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2021-04-08 US disclosed
US-10813909-B2 Triple drug combination (metformin, simvastatin, digoxin) for targeted treatment of pancreatic cancer THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2020-10-27 US disclosed
EP-3458033-A2 TRIPLE DRUG COMBINATION (METFORMIN, SIMVASTATIN, DIGOXIN) FOR TARGETED TREATMENT OF PANCREATIC CANCER THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2019-03-27 EP disclosed
WO-2018044369-A2 TRIPLE DRUG COMBINATION (METFORMIN, SIMVASTATIN, DIGOXIN) FOR TARGETED TREATMENT OF PANCREATIC CANCER THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2018-03-08 WO disclosed
EP-1014941-B2 HOT-MELT EXTRUDABLE PHARMACEUTICAL FORMULATION UNIV TEXAS (US) 2017-05-17 EP disclosed
US-9198865-B2 Biologically active composition comprising ethylcellulose DOW GLOBAL TECHNOLOGIES LLC 2015-12-01 US disclosed
EP-2272536-A2 Hot-melt extrudable Pharmaceutical formulation Board of Regents, The University of Texas System (US) 2011-01-12 EP disclosed
EP-1978940-B1 BIOLOGICALLY ACTIVE COMPOSITION COMPRISING ETHYLCELLULOSE DOW GLOBAL TECHNOLOGIES INC (US) 2010-12-29 EP disclosed
EP-1978940-A2 BIOLOGICALLY ACTIVE COMPOSITION COMPRISING ETHYLCELLULOSE DOW GLOBAL TECHNOLOGIES INC. (US) 2008-10-15 EP disclosed
WO-2007084212-A2 BIOLOGICALLY ACTIVE COMPOSITION COMPRISING ETHYLCELLULOSE DOW GLOBAL TECHNOLOGIES INC. (US) 2007-07-26 WO disclosed
US-20060251724-A1 Method for preparing thermoformed compositions containing acrylic polymer binders, pharmaceutical dosage forms and methods of preparing the same BPSI HOLDINGS, INC. 2006-11-09 US disclosed
EP-1624859-A2 METHOD FOR PREPARING THERMOFORMED COMPOSITIONS CONTAINING ACRYLIC POLYMER BINDERS, PHARMACEUTUAL DOSAGE FORMS AND METHODS OF PREPARING THE SAME BPSI Holdings, Inc. (US) 2006-02-15 EP disclosed
EP-1014941-A4 HOT-MELT EXTRUDABLE PHARMACEUTICAL FORMULATION UNIV TEXAS (US) 2005-11-09 EP disclosed
WO-2004100883-A2 METHOD FOR PREPARING THERMOFORMED COMPOSITIONS CONTAINING ACRYLIC POLYMER BINDERS, PHARMACEUTUAL DOSAGE FORMS AND METHODS OF PREPARING THE SAME BPSI HOLDINGS, INC. (US) 2004-11-25 WO disclosed
US-6488963-B1 POLYETHYLENE OXIDE FORMULATIONS THAT ARE NOT FILM-LIKE PREPARATIONS; CONTROLLED DRUG DELIVERY THE UNIVERSITY OF TEXAS SYSTEM 2002-12-03 US disclosed
EP-1014941-A1 HOT-MELT EXTRUDABLE PHARMACEUTICAL FORMULATION THE BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2000-07-05 EP disclosed
WO-1997049384-A1 HOT-MELT EXTRUDABLE PHARMACEUTICAL FORMULATION BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1997-12-31 WO disclosed
US-5143731-A Administering hyperosmotic, isoosmotic, or hypoosmotic thermo-irreversible gel as drug vehicle MEDIVENTURES INCORPORATED (US) 1992-09-01 US disclosed