Cloranolol

Cloranolol

SCHEMBL1649063

CC(C)(C)NCC(O)COc1cc(Cl)ccc1Cl.[Cl-].[H+]

nearest known ligand 0.59

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Cloranolol. 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
ACHE known ✓ P22303 1/20 0.52
CHRM1 known ✓ P11229 1/20 0.47
SLC6A2 known ✓ P23975 1/20 0.47
SLC2A1 P11166 1/20 0.59
KMT2A Q03164 3/20 0.58
MEN1 O00255 2/20 0.58
HTT P42858 1/20 0.58
ADRB2 P07550 4/20 0.55
ADRB1 P08588 3/20 0.55
ADRB3 P13945 2/20 0.55
MAPT P10636 2/20 0.52
CYP2D6 P10635 3/20 0.51
HTR1A P08908 2/20 0.50
ADRA2A P08913 2/20 0.50
ADRA2B P18089 1/20 0.50
MAOA P21397 1/20 0.50
HTR2B P41595 1/20 0.50
GLA P06280 1/20 0.48
L3MBTL1 Q9Y468 1/20 0.47
USP2 O75604 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
Cloranolol SCHEMBL80493 0.97 SLC2A1 (0.62) SLC2A1KMT2AMEN1HTTADRB2
Cloranolol SCHEMBL80494 0.97 SLC2A1 (0.62) SLC2A1KMT2AMEN1HTTADRB2
Cloranolol SCHEMBL1230787 0.96 KMT2A (0.63) SLC2A1KMT2AMEN1HTTADRB2
Cloranolol SCHEMBL1230788 0.96 KMT2A (0.63) SLC2A1KMT2AMEN1HTTADRB2
Bupranolol SCHEMBL29518497 0.85 L3MBTL1 (0.63) SLC2A1KMT2AMEN1HTTADRB2
Bupranolol SCHEMBL123717 0.85 L3MBTL1 (0.63) SLC2A1KMT2AMEN1HTTADRB2
Bupranolol SCHEMBL34061 0.85 L3MBTL1 (0.63) SLC2A1KMT2AMEN1HTTADRB2
Bupranolol SCHEMBL2497819 0.85 L3MBTL1 (0.63) SLC2A1KMT2AMEN1HTTADRB2
Bupranolol SCHEMBL6508337 0.85 L3MBTL1 (0.63) SLC2A1KMT2AMEN1HTTADRB2
Bupranolol SCHEMBL348362 0.84 L3MBTL1 (0.65) SLC2A1KMT2AMEN1HTTADRB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7927613-B2 Pharmaceutical co-crystal compositions UNIVERSITY OF SOUTH FLORIDA (US) 2011-04-19 US disclosed
EP-1303306-B1 EPOXY-STEROIDAL ALDOSTERONE ANTAGONIST AND BETA-ADRENERGIC ANTAGONIST COMBINATION THERAPY FOR TREATMENT OF CONGESTIVE HEART FAILURE PHARMACIA CORP (US) 2006-06-21 EP disclosed
US-20050215537-A1 Epoxy-steroidal aldosterone antagonist and beta-adrenergic antagonist combination therapy for treatment of congestive heart failure PHARMACIA CORPORATION 2005-09-29 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 (1 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-20050215537-A1 Epoxy-steroidal aldosterone antagonist and beta-adrenergic antagonist combination therapy for treatment of congestive heart failure ADRB1, ADRB2, ADRB3 ACHE 2465/4885CHRM1 580/4885SLC6A2 637/4885

“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.