Bupranolol

Bupranolol

SCHEMBL348362

Cc1ccc(Cl)c(OC[C@@H](O)CNC(C)(C)C)c1.Cl

nearest known ligand 0.65

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
GLA known ✓ P06280 1/20 0.58
ACHE known ✓ P22303 1/20 0.55
ADRB2 known ✓ P07550 2/20 0.51
ADRB1 known ✓ P08588 1/20 0.51
HTR1A known ✓ P08908 1/20 0.50
ADRA2A known ✓ P08913 1/20 0.50
ADRA2B known ✓ P18089 1/20 0.50
MAOA known ✓ P21397 1/20 0.50
HTR2B known ✓ P41595 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.65
KMT2A Q03164 3/20 0.65
MEN1 O00255 2/20 0.65
HTT P42858 1/20 0.65
MAPT P10636 3/20 0.58
NPSR1 Q6W5P4 1/20 0.55
CYP2D6 P10635 2/20 0.54
SLC2A1 P11166 1/20 0.53
KDM4E B2RXH2 1/20 0.50
ALDH1A1 P00352 1/20 0.50

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
Bupranolol SCHEMBL348360 1.00 L3MBTL1 (0.65) L3MBTL1KMT2AMEN1HTTMAPT
Bupranolol SCHEMBL6508337 0.99 L3MBTL1 (0.63) L3MBTL1KMT2AMEN1HTTMAPT
Bupranolol SCHEMBL2497819 0.99 L3MBTL1 (0.63) L3MBTL1KMT2AMEN1HTTMAPT
Bupranolol SCHEMBL123717 0.99 L3MBTL1 (0.63) L3MBTL1KMT2AMEN1HTTMAPT
Bupranolol SCHEMBL29518497 0.99 L3MBTL1 (0.63) L3MBTL1KMT2AMEN1HTTMAPT
Bupranolol SCHEMBL34061 0.99 L3MBTL1 (0.63) L3MBTL1KMT2AMEN1HTTMAPT
SCHEMBL348361 0.91 L3MBTL1 (0.63) L3MBTL1KMT2AMEN1HTTMAPT
Bupranolol SCHEMBL8908385 0.89 L3MBTL1 (0.53) L3MBTL1KMT2AMEN1HTTMAPT
Cloranolol SCHEMBL1230788 0.88 KMT2A (0.63) L3MBTL1KMT2AMEN1HTTMAPT
Cloranolol SCHEMBL1230787 0.88 KMT2A (0.63) L3MBTL1KMT2AMEN1HTTMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2768514-A1 LOCALIZED MODULATION OF TISSUES AND CELLS TO ENHANCE THERAPEUTIC EFFECTS INCLUDING RENAL DENERVATION Mercator Medsystems, Inc. (US) 2014-08-27 EP claimed
US-20130252932-A1 LOCALIZED MODULATION OF TISSUES AND CELLS TO ENHANCE THERAPEUTIC EFFECTS INCLUDING RENAL DENERVATION MERCATOR MEDSYSTEMS, INC. (US) 2013-09-26 US claimed
WO-2013059735-A1 LOCALIZED MODULATION OF TISSUES AND CELLS TO ENHANCE THERAPEUTIC EFFECTS INCLUDING RENAL DENERVATION MERCATOR MEDSYSTEMS, INC. (US) 2013-04-25 WO claimed
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 US claimed
US-5700410-A Method of manufacturing wax matrices NIPPON SHINYAKU CO., LTD. (JP) 1997-12-23 US claimed
US-5288503-A WATER-PERMEABLE DIFFUSION BARRIER OF POLYVINYL ALCOHOL SRCHEM INCORPORATED (US) 1994-02-22 US claimed
US-5260066-A Cryogel bandage containing therapeutic agent SRCHEM INCORPORATED (US) 1993-11-09 US claimed
JP-63104913-A None JP disclosed
JP-52154528-A None JP disclosed
US-20260144747-A1 SYRUP PREPARATION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2026-05-28 US disclosed
US-12564594-B2 Pharmaceutical composition containing 9-ethyl-6, 6-dimethyl-8-(4-morpholin-4-yl-piperidin-1-yl)-11-oxo-6, 11-dihydro-5H-benzo[b]carbazole-3-carbonitrile CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2026-03-03 US disclosed
EP-4606435-A2 PHARMACEUTICAL COMPOSITION COMPRISING POORLY SOLUBLE BASIC AGENT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-08-27 EP disclosed
EP-4316598-B1 PHARMACEUTICAL COMPOSITION COMPRISING A POORLY SOLUBLE BASIC AGENT CHUGAI PHARMACEUTICAL CO LTD (JP) 2025-06-18 EP disclosed
EP-0073819-A4 NASAL ADMINISTRATION OF BETA-BLOCKERS AND DOSAGE FORMS THEREFOR. UNIV KENTUCKY RES FOUND (US) 1984-11-16 EP disclosed
US-4428883-A NASAL OINTMENTS OR GELS THE UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 1984-01-31 US disclosed
EP-0073819-A1 NASAL ADMINISTRATION OF BETA-BLOCKERS AND DOSAGE FORMS THEREFOR. UNIV KENTUCKY RES FOUND (US) 1983-03-16 EP disclosed
WO-1982003009-A1 NASAL ADMINISTRATION OF BETA-BLOCKERS AND DOSAGE FORMS THEREFOR UNIV KENTUCKY RES FOUND (US) 1982-09-16 WO disclosed
EP-0037622-A2 Drug delivery insert for controlled ocular therapy ALZA CORPORATION (US) 1981-10-14 EP disclosed
US-4281654-A Drug delivery system for controlled ocular therapy ALZA CORPORATION (US) 1981-08-04 US disclosed
JP-S52154528-A REMEDY FOR GLAUCOMA KAKEN PHARMACEUT CO LTD 1977-12-22 JP 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-12564594-B2 Pharmaceutical composition containing 9-ethyl-6, 6-dimethyl-8-(4-morpholin-4-yl-piperidin-1-yl)-11-oxo-6, 11-dihydro-5H-benzo[b]carbazole-3-carbonitrile KCNN2, KCNN1, KIT GLA 2750/4885ACHE 1719/4885ADRB2 2077/4885
US-20260144747-A1 SYRUP PREPARATION ALK, IRAK1, IRAK3 GLA 4454/4885ACHE 3413/4885ADRB2 2541/4885

“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.