Bepotastine

Bepotastine

SCHEMBL2804852

O=C(O)CCCN1CCC(O[C@@H](c2ccc(Cl)cc2)c2ccccn2)CC1.O=C(O)c1ccccc1

nearest known ligand 0.54

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HRH1

The experimentally established mechanism targets of Bepotastine. 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
HRH1 known ✓ P35367 1/20 0.47
BCHE P06276 7/20 0.54
DRD2 P14416 8/20 0.47
NPC1 O15118 1/20 0.47
MLNR O43193 1/20 0.47
NR1I2 O75469 1/20 0.47
EGFR P00533 1/20 0.47
LMNA P02545 1/20 0.47
ERBB2 P04626 1/20 0.47
FYN P06241 1/20 0.47
CHRM2 P08172 1/20 0.47
CHRM4 P08173 1/20 0.47
ABCB1 P08183 1/20 0.47
ADRB1 P08588 1/20 0.47
HTR1A P08908 1/20 0.47
CHRM5 P08912 1/20 0.47
ADRA2A P08913 1/20 0.47
ADORA3 P0DMS8 1/20 0.47
CHRM1 P11229 1/20 0.47
ADRB3 P13945 1/20 0.47

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
Bepotastine SCHEMBL30200949 0.95 BCHE (0.55) BCHEDRD2NPC1MLNRNR1I2
Bepotastine SCHEMBL29459 0.95 BCHE (0.55) BCHEDRD2NPC1MLNRNR1I2
Bepotastine SCHEMBL5151702 0.95 BCHE (0.55) BCHEDRD2NPC1MLNRNR1I2
Bepotastine SCHEMBL29440897 0.95 BCHE (0.55) BCHEDRD2NPC1MLNRNR1I2
Bepotastine SCHEMBL726880 0.95 BCHE (0.55) BCHEDRD2NPC1MLNRNR1I2
Bepotastine SCHEMBL2803678 0.95 BCHE (0.55) BCHEDRD2NPC1MLNRNR1I2
Bepotastine SCHEMBL2808049 0.95 BCHE (0.55) BCHEDRD2NPC1MLNRNR1I2
Bepotastine SCHEMBL2806225 0.95 BCHE (0.55) BCHEDRD2NPC1MLNRNR1I2
Bepotastine SCHEMBL2807641 0.95 BCHE (0.55) BCHEDRD2NPC1MLNRNR1I2
SCHEMBL28391952 0.92 BCHE (0.56) BCHEDRD2NPC1MLNRNR1I2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100137367-A1 NOVEL CRYSTALLINE BEPOTASTINE METAL SALT HYDRATE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME HANMI PHARM. CO., LTD. (KR) 2010-06-03 US disclosed
EP-2144896-A1 NOVEL CRYSTALLINE BEPOTASTINE METAL SALT HYDRATE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME Hanmi Pharm. Co., Ltd. (KR) 2010-01-20 EP disclosed
WO-2008123701-A1 NOVEL CRYSTALLINE BEPOTASTINE METAL SALT HYDRATE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME HANMI PHARM. CO., LTD. (KR) 2008-10-16 WO disclosed
US-7282589-B2 Acid addition salt of optically active piperidine compound and process for preparing the same UBE INDUSTRIES, LTD. (JP) 2007-10-16 US disclosed
US-20040220226-A1 Acid addition salt of optically active piperidine compound and process for preparing the same UBE INDUSTRIES, LTD. 2004-11-04 US disclosed
US-6780877-B2 ANTIHISTAMINIC ACTIVITY, ANTI-ALLERGIC ACTIVITY UBE INDUSTRIES, LTD. (JP) 2004-08-24 US disclosed
EP-0949260-B1 ACID-ADDITION SALTS OF OPTICALLY ACTIVE PIPERIDINE COMPOUND AND PROCESS FOR PRODUCING THE SAME UBE INDUSTRIES (JP) 2002-05-22 EP disclosed
US-20020026054-A1 Acid addition salt of optically active piperidine compound and process for preparing the same UBE INDUSTRIES, LTD. 2002-02-28 US disclosed
US-6307052-B1 Acid-addition salts of optically active piperidine compound and process for producing the same UBE INDUSTRIES, LTD. (JP) 2001-10-23 US disclosed
EP-0949260-A1 ACID-ADDITION SALTS OF OPTICALLY ACTIVE PIPERIDINE COMPOUND AND PROCESS FOR PRODUCING THE SAME UBE INDUSTRIES, LTD. (JP) 1999-10-13 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 (3 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-20100137367-A1 NOVEL CRYSTALLINE BEPOTASTINE METAL SALT HYDRATE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME HRH1, NOTUM, HRH2 HRH1 1/4885BCHE 41/4885DRD2 4080/4885
US-20020026054-A1 Acid addition salt of optically active piperidine compound and process for preparing the same CMA1, HRH1, HRH2 HRH1 2/4885BCHE 966/4885DRD2 1620/4885
US-20040220226-A1 Acid addition salt of optically active piperidine compound and process for preparing the same DCTPP1, SSRP1, ITPA HRH1 988/4885BCHE 3465/4885DRD2 250/4885

“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.