Tolbutamide

Tolbutamide

SCHEMBL140363

CCCCNC(=O)NS(=O)(=O)c1ccc(C)cc1.O

nearest known ligand 0.97

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC8KCNJ11

The experimentally established mechanism targets of Tolbutamide. 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 5/20 0.97
LMNA P02545 3/20 0.97
CYP2C9 P11712 2/20 0.97
TSHR P16473 2/20 0.97
ALB P02768 1/20 0.97
TDP1 Q9NUW8 1/20 0.97
FBP1 P09467 7/20 0.69
NPSR1 Q6W5P4 2/20 0.61
CYP3A4 P08684 1/20 0.61
THRB P10828 1/20 0.61
NFKB1 P19838 1/20 0.61
HTR2A P28223 1/20 0.61
CYP2C19 P33261 1/20 0.61
ADRA1A P35348 1/20 0.61
SMN1; SMN2 Q16637 1/20 0.61
CA12 O43570 1/20 0.60
CA1 P00915 1/20 0.60
CA2 P00918 1/20 0.60
CA9 Q16790 1/20 0.60
MAPT P10636 1/20 0.56

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
Tolbutamide SCHEMBL15918 0.98 ALDH1A1 (1.00) ALDH1A1LMNACYP2C9TSHRALB
Tolbutamide SCHEMBL1536920 0.98 ALDH1A1 (1.00) ALDH1A1LMNACYP2C9TSHRALB
Tolbutamide SCHEMBL28046582 0.97 ALDH1A1 (0.97) ALDH1A1LMNACYP2C9TSHRALB
Tolbutamide SCHEMBL11356450 0.97 ALDH1A1 (0.97) ALDH1A1LMNACYP2C9TSHRALB
Tolbutamide SCHEMBL668223 0.97 ALDH1A1 (0.97) ALDH1A1LMNACYP2C9TSHRALB
Tolbutamide SCHEMBL4367531 0.97 ALDH1A1 (0.97) ALDH1A1LMNACYP2C9TSHRALB
Tolbutamide SCHEMBL28184306 0.97 ALDH1A1 (0.97) ALDH1A1LMNACYP2C9TSHRALB
Tolbutamide SCHEMBL11357518 0.97 ALDH1A1 (0.97) ALDH1A1LMNACYP2C9TSHRALB
Tolbutamide SCHEMBL7551276 0.97 ALDH1A1 (0.97) ALDH1A1LMNACYP2C9TSHRALB
Tolbutamide SCHEMBL8733982 0.96 ALDH1A1 (0.94) ALDH1A1LMNACYP2C9TSHRALB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12024519-B2 Fused ring derivative having MGAT-2 inhibitory activity SHIONOGI & CO., LTD. (JP) 2024-07-02 US disclosed
CN-117999257-A Bicyclic heterocyclic derivatives having virus proliferation inhibitory activity and pharmaceutical compositions containing the same 盐野义制药株式会社 2024-05-07 CN disclosed
CN-113501821-B Fused ring derivatives having MGAT-2 inhibitory activity 盐野义制药株式会社 2024-04-09 CN disclosed
CN-112533922-B Polycyclic pyridone derivatives 盐野义制药株式会社 2024-03-22 CN disclosed
EP-3653625-B1 FUSED RING DERIVATIVE HAVING MGAT-2 INHIBITORY ACTIVITY SHIONOGI & CO (JP) 2024-02-07 EP disclosed
CN-117362306-A Amide derivatives having antiviral activity 盐野义制药株式会社 2024-01-09 CN disclosed
CN-117327072-A Polycyclic carbamoyl pyridone derivatives 盐野义制药株式会社 2024-01-02 CN disclosed
EP-4257137-A2 POLYCYCLIC CARBAMOYLPYRIDONE DERIVATIVES FOR THE TREATMENT OF HIV Shionogi & Co., Ltd (JP) 2023-10-11 EP disclosed
CN-112513042-B Polycyclic carbamoyl pyridone derivatives 盐野义制药株式会社 2023-09-29 CN disclosed
CN-116528850-A Amide derivatives having antiviral activity 盐野义制药株式会社 2023-08-01 CN disclosed
CN-103140221-A Novel heterocyclic derivatives and pharmaceutical composition containing same SHIONOGI & CO 2013-06-05 CN disclosed
EP-2511269-A1 FUSED HETEROCYCLIC COMPOUND HAVING AMINO GROUP Shionogi & Co., Ltd. (JP) 2012-10-17 EP disclosed
EP-2511268-A1 OXAZINE DERIVATIVE Shionogi & Co., Ltd. (JP) 2012-10-17 EP disclosed
US-20120245155-A1 FUSED HETEROCYCLIC COMPOUND HAVING AMINO GROUP SHIONOGI & CO., LTD. (JP) 2012-09-27 US disclosed
US-20120238557-A1 AMINOTHIAZINE OR AMINOOXAZINE DERIVATIVE HAVING AMINO LINKER SHIONOGI & CO., LTD. (JP) 2012-09-20 US disclosed
EP-2500344-A1 AMINOTHIAZINE OR AMINOOXAZINE DERIVATIVE HAVING AMINO LINKER Shionogi&Co., Ltd. (JP) 2012-09-19 EP disclosed
EP-2460805-A1 FUSED IMIDAZOLE DERIVATIVE HAVING TTK INHIBITORY ACTION Oncotherapy Science, Inc. (JP) 2012-06-06 EP disclosed
US-20120059061-A1 NOVEL ANTI-INFLAMMATORY COMPOUNDS THE UNIVERSITY OF TOKYO (JP) 2012-03-08 US disclosed
US-20120059162-A1 FUSED IMIDAZOLE DERIVATIVE HAVING TTK INHIBITORY ACTION ONCOTHERAPY SCIENCE, INC. (JP) 2012-03-08 US disclosed
EP-2415748-A1 NOVEL ANTI-INFLAMMATORY COMPOUNDS The University of Tokyo (JP) 2012-02-08 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-20120059162-A1 FUSED IMIDAZOLE DERIVATIVE HAVING TTK INHIBITORY ACTION NR0B1, GRK7, NR5A2 ALDH1A1 3128/4885LMNA 3669/4885CYP2C9 3302/4885
US-20120238557-A1 AMINOTHIAZINE OR AMINOOXAZINE DERIVATIVE HAVING AMINO LINKER APP, APBA1, SLC1A5 ALDH1A1 2660/4885LMNA 2574/4885CYP2C9 2591/4885
US-20120059061-A1 NOVEL ANTI-INFLAMMATORY COMPOUNDS ALOX15, ALOX15B, ALOX12 ALDH1A1 1074/4885LMNA 4387/4885CYP2C9 1084/4885
US-20120245155-A1 FUSED HETEROCYCLIC COMPOUND HAVING AMINO GROUP APP, IAPP, BACE1 ALDH1A1 3901/4885LMNA 873/4885CYP2C9 1417/4885
US-12024519-B2 Fused ring derivative having MGAT-2 inhibitory activity MGAT2, MGAT1, ACAT2 ALDH1A1 1270/4885LMNA 4291/4885CYP2C9 2930/4885

“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.