Carazolol

Carazolol

SCHEMBL7530148

CC(C)NCC(O)COc1cccc2[nH]c3ccccc3c12.Cl

nearest known ligand 0.98

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 Carazolol. 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
ADRB2 known ✓ P07550 10/20 0.98
ADRB1 known ✓ P08588 7/20 0.66
ADRB3 known ✓ P13945 7/20 0.66
HTR1A known ✓ P08908 6/20 0.66
HTR2C known ✓ P28335 5/20 0.66
SIGMAR1 known ✓ Q99720 4/20 0.66
HTR2A known ✓ P28223 4/20 0.66
HTR6 known ✓ P50406 4/20 0.66
DRD3 known ✓ P35462 4/20 0.66
ADRA2A known ✓ P08913 3/20 0.66
SLC6A2 known ✓ P23975 3/20 0.66
OPRM1 known ✓ P35372 3/20 0.66
PTGS1 known ✓ P23219 1/20 0.66
SLC6A4 known ✓ P31645 4/20 0.64
HTR2B known ✓ P41595 4/20 0.64
ADRA1A known ✓ P35348 3/20 0.64
OPRK1 known ✓ P41145 3/20 0.64
SCN1A known ✓ P35498 2/20 0.64
SCN2A known ✓ Q99250 2/20 0.64
SCN3A known ✓ Q9NY46 2/20 0.64

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
Carazolol SCHEMBL10568418 1.00 ADRB2 (0.98) ADRB2DNM1ADRB1ADRB3HTR1A
Carazolol SCHEMBL6511163 0.99 ADRB2 (1.00) ADRB2DNM1ADRB1ADRB3HTR1A
Carazolol SCHEMBL29354289 0.99 ADRB2 (1.00) ADRB2DNM1ADRB1ADRB3HTR1A
Carazolol SCHEMBL77901 0.99 ADRB2 (1.00) ADRB2DNM1ADRB1ADRB3HTR1A
Carazolol SCHEMBL77903 0.99 ADRB2 (1.00) ADRB2DNM1ADRB1ADRB3HTR1A
SCHEMBL2992432 0.87 ADRB2 (0.79) ADRB2DNM1ADRB1ADRB3HTR1A
Fluorocarazolol SCHEMBL14155316 0.87 ADRB2 (0.79) ADRB2DNM1ADRB1ADRB3HTR1A
SCHEMBL3002063 0.86 ADRB2 (0.78) ADRB2DNM1ADRB1ADRB3HTR1A
SCHEMBL13495721 0.85 ADRB2 (0.76) ADRB2DNM1ADRB1ADRB3HTR1A
SCHEMBL12407602 0.84 ADRB2 (0.74) ADRB2DNM1ADRB1ADRB3HTR1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106390128-A USE OF BETA-ADRENERGIC INVERSE AGONISTS FOR SMOKING CESSATION 伊沃恩有限公司 2017-02-15 CN disclosed
EP-1189596-A1 PHARMACEUTICAL COMPOSITION FOR NASALLY ADMINISTERING WATER-SOLUBLE ACTIVE SUBSTANCES Klöcker, Norbert, Dr.med. (DE) 2002-03-27 EP disclosed
WO-2000074652-A1 PHARMACEUTICAL COMPOSITION FOR NASALLY ADMINISTERING WATER-SOLUBLE ACTIVE SUBSTANCES HEXAL AG (DE) 2000-12-14 WO disclosed
WO-1995020568-A1 PHARMACEUTICAL PRODUCT COMPRISING A SALICYLATE OF AN ESTERIFIABLE BETA-BLOCKER CAL INTERNATIONAL LIMITED (IE) 1995-08-03 WO disclosed
US-4849530-A Process for the preparation of crystalline salts or aryloxy-propanolamines RORER PHARMACEUTICAL CORPORATION (US) 1989-07-18 US disclosed
EP-0229947-A1 Novel crystalline salts of aryloxy-propanolamines, their preparation and their use RORER INTERNATIONAL (OVERSEAS) INC. (US) 1987-07-29 EP disclosed
EP-0004920-B1 DERIVATIVES OF CARBAZOLYL-4-OXYPROPANOLAMINE, METHODS FOR THEIR PREPARATION AND MEDICINES CONTAINING THEM Roche Diagnostics GmbH (DE) 1981-08-05 EP disclosed