Indenolol

Indenolol

SCHEMBL1650473

CC(C)NCC(O)COc1cccc2c1C=CC2.[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 Indenolol. 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
▸ SLC6A2 known ✓ P23975 1/20 0.54
▸ SLC6A3 known ✓ Q01959 1/20 0.50
▸ ADRB2 P07550 11/20 0.54
▸ ADRB1 P08588 11/20 0.54
▸ ADRB3 P13945 5/20 0.54
▸ CYP1A2 P05177 5/20 0.54
▸ CYP2D6 P10635 5/20 0.54
▸ SIGMAR1 Q99720 4/20 0.54
▸ SLC6A4 P31645 4/20 0.54
▸ HTR2A P28223 4/20 0.54
▸ HTR2C P28335 4/20 0.54
▸ HTR1A P08908 4/20 0.54
▸ LMNA P02545 4/20 0.54
▸ HTR2B P41595 3/20 0.54
▸ NR2E1 Q9Y466 3/20 0.54
▸ ALDH1A1 P00352 3/20 0.54
▸ HTR6 P50406 3/20 0.54
▸ TSHR P16473 3/20 0.54
▸ MAPK1 P28482 3/20 0.54
▸ ADRA1A P35348 3/20 0.54

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
Indenolol SCHEMBL79023 0.98 ADRB2 (0.56) ADRB2ADRB1ADRB3CYP1A2CYP2D6
Indenolol SCHEMBL79021 0.98 ADRB2 (0.56) ADRB2ADRB1ADRB3CYP1A2CYP2D6
Indenolol SCHEMBL349116 0.96 ADRB2 (0.57) ADRB2ADRB1ADRB3CYP1A2CYP2D6
Indenolol SCHEMBL349114 0.96 ADRB2 (0.57) ADRB2ADRB1ADRB3CYP1A2CYP2D6
SCHEMBL11631654 0.90 ADRB2 (0.47) ADRB2ADRB1ADRB3CYP1A2CYP2D6
SCHEMBL11656702 0.87 ADRB2 (0.44) ADRB2ADRB1ADRB3CYP1A2CYP2D6
Idropranolol SCHEMBL1255318 0.86 ADRB1 (0.54) ADRB2ADRB1ADRB3CYP1A2CYP2D6
Indenolol SCHEMBL11666579 0.84 ADRB2 (0.48) ADRB2ADRB1ADRB3CYP1A2CYP2D6
SCHEMBL11754160 0.83 ALOX15 (0.41) ADRB2ADRB1ADRB3CYP1A2CYP2D6
Hydrochloric Acid SCHEMBL11659927 0.82 ADRB2 (0.46) ADRB2ADRB1ADRB3CYP1A2CYP2D6

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 SLC6A2 637/4885SLC6A3 2232/4885ADRB2 2/4885

“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.

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