Dilevalol

Dilevalol

SCHEMBL588720

C[C@H](CCc1ccccc1)NC[C@H](O)c1ccc(O)c(C(N)=O)c1.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRB1ADRB2ADRB3

The experimentally established mechanism targets of Dilevalol. 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
ADRB1 known ✓ P08588 14/20 1.00
ADRB2 known ✓ P07550 14/20 1.00
ADRB3 known ✓ P13945 12/20 1.00
ADRA1A P35348 14/20 1.00
ADRA1D P25100 13/20 1.00
ADRA1B P35368 13/20 1.00
KDM4E B2RXH2 2/20 1.00
ALDH1A1 P00352 2/20 1.00
LMNA P02545 2/20 1.00
ADRA2A P08913 2/20 1.00
HPGD P15428 2/20 1.00
HSD17B10 Q99714 2/20 1.00
GAA P10253 1/20 1.00
ADRA2B P18089 1/20 1.00
ADRA2C P18825 1/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
CYP2D6 P10635 2/20 0.98
HTR1A P08908 2/20 0.98
SLC6A2 P23975 2/20 0.98
SLC6A4 P31645 2/20 0.98

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
Labetalol SCHEMBL9614383 1.00 ADRB1 (1.00) ADRB1ADRA1AADRB2ADRA1DADRA1B
Labetalol SCHEMBL10450118 1.00 ADRB1 (1.00) ADRB1ADRA1AADRB2ADRA1DADRA1B
Labetalol SCHEMBL41230 1.00 ADRB1 (1.00) ADRB1ADRA1AADRB2ADRA1DADRA1B
Labetalol SCHEMBL29710409 1.00 ADRB1 (1.00) ADRB1ADRA1AADRB2ADRA1DADRA1B
Labetalol SCHEMBL10356800 0.99 ADRB1 (1.00) ADRB1ADRA1AADRB2ADRA1DADRA1B
Labetalol SCHEMBL4582 0.99 ADRB1 (1.00) ADRB1ADRA1AADRB2ADRA1DADRA1B
Dilevalol SCHEMBL79468 0.99 ADRB1 (1.00) ADRB1ADRA1AADRB2ADRA1DADRA1B
Labetalol SCHEMBL7273474 0.99 ADRB1 (1.00) ADRB1ADRA1AADRB2ADRA1DADRA1B
Labetalol SCHEMBL41231 0.99 ADRB1 (1.00) ADRB1ADRA1AADRB2ADRA1DADRA1B
Labetalol SCHEMBL10882744 0.99 ADRB1 (1.00) ADRB1ADRA1AADRB2ADRA1DADRA1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2205639-B1 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS MERCK SHARP & DOHME (US) 2015-12-23 EP claimed
US-20140161798-A1 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS MERCK SHARP & DOHME CORP. (US) 2014-06-12 US claimed
US-8268352-B2 Modified release composition for highly soluble drugs TORRENT PHARMACEUTICALS LIMITED (IN) 2012-09-18 US claimed
US-8263125-B2 Dosage form for high dose-high solubility active ingredients that provides for immediate release and modified release of the active ingredients TORRENT PHARMACEUTICALS LIMITED (IN) 2012-09-11 US claimed
WO-2012054438-A1 ANTI-PCSK9 SCHERING CORPORATION (US) 2012-04-26 WO claimed
CN-102232088-A Anti-PCSK9 and methods for treating lipid and cholesterol disorders SCHERING CORP 2011-11-02 CN claimed
US-20110033465-A1 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS SCHERING CORPORATION (US) 2011-02-10 US claimed
EP-2205639-A2 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS SCHERING CORPORATION (US) 2010-07-14 EP claimed
WO-2009055783-A2 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS SCHERING CORPORATION (US) 2009-04-30 WO claimed
EP-1363668-B1 COMBINATIONS OF BILE ACID SEQUESTRANT(S) AND STEROL ABSORPTION INHIBITOR(S) AND TREATMENTS FOR VASCULAR INDICATIONS SCHERING CORP (US) 2007-08-15 EP claimed
US-20060024365-A1 Novel dosage form VAYA NAVIN 2006-02-02 US claimed
US-20060018933-A1 Novel drug delivery system TORRENT PHARMACEUTICALS LIMITED (IN) 2006-01-26 US claimed
US-20060018934-A1 Novel drug delivery system TORRENT PHARMACEUTICALS LIMITED (IN) 2006-01-26 US claimed
EP-1541175-A2 Combinations of sterol absorption inhibitor(s) with cardiovascular agent(s) for the treatment of vascular conditions Schering Corporation (US) 2005-06-15 EP claimed
CN-1582168-A Combinations of sterol absorption inhibitor(s) with cardiovascular agent(s) for the treatment of vascular conditions SCHERING CORP (US) 2005-02-16 CN claimed
EP-1385548-A2 COMBINATIONS OF STEROL ABSORPTION INHIBITOR(S) WITH CARDIOVASCULAR AGENT(S) FOR THE TREATMENT OF VASCULAR CONDITIONS Schering Corporation (US) 2004-02-04 EP claimed
US-20030069221-A1 Combinations of sterol absorption inhibitor(s) with cardiovascular agent(s) for the treatment of vascular conditions SCHERING CORPORATION 2003-04-10 US claimed
US-20020115655-A1 Such as S-(4-methoxybenzyl)-N-(2-(N',N'-dimethylamino)ethyl) thiosalicylamide; for treatment of cardiovascular disorders MASSACHUSETTS COLLEGE OF PHARMACY 2002-08-22 US claimed
WO-2002058731-A2 COMBINATIONS OF STEROL ABSORPTION INHIBITOR(S) WITH CARDIOVASCULAR AGENT(S) FOR THE TREATMENT OF VASCULAR CONDITIONS SCHERING CORPORATION (US) 2002-08-01 WO claimed
US-4619919-A (1)-5-(R)-1-HYDROXY-2(R)-(1-METHYL-3-PHENYLPROPYL)AMINO)ETHYL) SALICYLAMIDE SCHERING CORPORATION (US) 1986-10-28 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 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-20110033465-A1 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS PCSK9, PCSK7, CETP ADRB1 3264/4885ADRB2 4211/4885ADRB3 2783/4885
US-20030069221-A1 Combinations of sterol absorption inhibitor(s) with cardiovascular agent(s) for the treatment of vascular conditions CYP46A1, FABP2, SREBF1 ADRB1 193/4885ADRB2 346/4885ADRB3 264/4885
US-20140161798-A1 ANTI-PCSK9 AND METHODS FOR TREATING LIPID AND CHOLESTEROL DISORDERS PCSK9, PCSK7, CETP ADRB1 3264/4885ADRB2 4211/4885ADRB3 2783/4885
US-20020115655-A1 Such as S-(4-methoxybenzyl)-N-(2-(N',N'-dimethylamino)ethyl) thiosalicylamide; for treatment of cardiovascular disorders CACNA1G, CACNA1F, CACNA1H ADRB1 309/4885ADRB2 246/4885ADRB3 410/4885

“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.