Rebamipide

Rebamipide

SCHEMBL2859632

NC(CO)(CO)CO.O=C(NC(Cc1cc(=O)[nH]c2ccccc12)C(=O)O)c1ccc(Cl)cc1

nearest known ligand 0.87

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DHFRGARTPTGFRPTGIRPTGS1PTGS2TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8envmurAthyA

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

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
UBASH3B Q8TF42 1/20 0.87
ERAP2 Q6P179 1/20 0.51
PPARG P37231 1/20 0.50
ITGB2 P05107 5/20 0.49
ICAM1 P05362 5/20 0.49
ITGAL P20701 5/20 0.49
F11 P03951 2/20 0.49
TACR1 P25103 2/20 0.47
CA2 P00918 1/20 0.45
CCKBR P32239 3/20 0.45
MEN1 O00255 1/20 0.44
KMT2A Q03164 1/20 0.44
PIN1 Q13526 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
Rebamipide SCHEMBL23346201 0.93 UBASH3B (1.00) UBASH3BERAP2PPARGITGB2ICAM1
Rebamipide SCHEMBL29560992 0.93 UBASH3B (1.00) UBASH3BERAP2PPARGITGB2ICAM1
Rebamipide SCHEMBL221527 0.93 UBASH3B (1.00) UBASH3BERAP2PPARGITGB2ICAM1
Rebamipide SCHEMBL5794018 0.93 UBASH3B (1.00) UBASH3BERAP2PPARGITGB2ICAM1
Rebamipide SCHEMBL21623658 0.93 UBASH3B (1.00) UBASH3BERAP2PPARGITGB2ICAM1
Rebamipide SCHEMBL9114879 0.92 UBASH3B (0.98) UBASH3BERAP2PPARGITGB2ICAM1
Rebamipide SCHEMBL28798513 0.92 UBASH3B (0.98) UBASH3BERAP2PPARGITGB2ICAM1
Rebamipide SCHEMBL2292009 0.92 UBASH3B (0.98) UBASH3BERAP2PPARGITGB2ICAM1
Rebamipide SCHEMBL27858766 0.92 UBASH3B (0.98) UBASH3BERAP2PPARGITGB2ICAM1
Rebamipide SCHEMBL26607917 0.92 UBASH3B (0.98) UBASH3BERAP2PPARGITGB2ICAM1

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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1706383-B1 Amine salt of carbostyril derivative useful for the treatment of, inter alia, gastric ulcer OTSUKA PHARMA CO LTD (JP) 2015-07-22 EP disclosed
US-8222276-B2 Amine salt of carbostyril derivative OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2012-07-17 US disclosed
EP-2253619-A1 Amine salt of carbostyril derivative Otsuka Pharmaceutical Co., Ltd. (JP) 2010-11-24 EP disclosed
US-20100210684-A1 Amine salt of carbostyril derivative OTSUKA PHARMACEUTICAL CO., LTD. 2010-08-19 US disclosed
US-7732611-B2 Amine salt of carbostyril derivative OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2010-06-08 US disclosed
US-20070155787-A1 Amine salt of carbostyril derivative OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2007-07-05 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 (2 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-20100210684-A1 Amine salt of carbostyril derivative SLC7A1, ARGLU1, JAK1 UBASH3B 1921/4885ERAP2 4336/4885PPARG 3499/4885
US-20070155787-A1 Amine salt of carbostyril derivative SLC7A1, ARGLU1, JAK1 UBASH3B 2005/4885ERAP2 4407/4885PPARG 3525/4885

“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.