Propranolol

Propranolol

SCHEMBL540824

CC(C)NCC(O)COc1cccc2[nH]ccc12.CC(C)NCC(O)COc1cccc2ccccc12

nearest known ligand 0.87

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRB1ADRB2

The experimentally established mechanism targets of Propranolol. 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 8/20 0.87
ADRB1 known ✓ P08588 7/20 0.87
HTR1A P08908 12/20 0.87
CYP1A2 P05177 5/20 0.87
ADRB3 P13945 5/20 0.87
CYP2D6 P10635 5/20 0.87
LMNA P02545 4/20 0.87
HTR2C P28335 4/20 0.87
ALDH1A1 P00352 4/20 0.87
TSHR P16473 3/20 0.87
MAPK1 P28482 3/20 0.87
DRD3 P35462 3/20 0.87
CYP3A4 P08684 2/20 0.87
CYP2C9 P11712 2/20 0.87
TP53 P04637 2/20 0.87
NFKB1 P19838 2/20 0.87
HTR1B P28222 2/20 0.87
ADRA1A P35348 2/20 0.87
OPRK1 P41145 2/20 0.87
TMEM97 Q5BJF2 2/20 0.87

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
Propranolol SCHEMBL20508988 0.99 HTR1A (0.85) HTR1AADRB2ADRB1CYP1A2ADRB3
Pindolol SCHEMBL29379249 0.93 HTR1A (1.00) HTR1AADRB2ADRB1CYP1A2ADRB3
Pindolol SCHEMBL29908300 0.93 HTR1A (1.00) HTR1AADRB2ADRB1CYP1A2ADRB3
Pindolol SCHEMBL1157882 0.93 HTR1A (1.00) HTR1AADRB2ADRB1CYP1A2ADRB3
Pindolol SCHEMBL5220 0.93 HTR1A (1.00) HTR1AADRB2ADRB1CYP1A2ADRB3
Pindolol SCHEMBL1157556 0.93 HTR1A (1.00) HTR1AADRB2ADRB1CYP1A2ADRB3
Pindolol SCHEMBL5219 0.93 HTR1A (1.00) HTR1AADRB2ADRB1CYP1A2ADRB3
Pindolol SCHEMBL2991558 0.92 HTR1A (0.97) HTR1AADRB2ADRB1CYP1A2ADRB3
Pindolol SCHEMBL561162 0.92 HTR1A (0.97) HTR1AADRB2ADRB1CYP1A2ADRB3
Pindolol SCHEMBL10494992 0.89 HTR1A (0.91) HTR1AADRB2ADRB1CYP1A2ADRB3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4374928-A2 NOVEL ALK2 INHIBITORS AND METHODS FOR INHIBITING BMP SIGNALING The Brigham And Women's Hospital Inc. (US) 2024-05-29 EP disclosed
EP-3615538-B1 NOVEL ALK2 INHIBITORS AND METHODS FOR INHIBITING BMP SIGNALING BRIGHAM & WOMENS HOSPITAL INC (US) 2024-02-07 EP disclosed
US-11654147-B2 ALK2 inhibitors and methods for inhibiting BMP signaling THE BRIGHAM AND WOMEN'S HOSPITAL, INC. (US) 2023-05-23 US disclosed
EP-2804669-B1 COMPOSITIONS AND METHODS OF USE OF PHORBOL ESTERS FOR THE TREATMENT OF STROKE BIOSUCCESS BIOTECH CO LTD (US) 2023-03-29 EP disclosed
US-20230000869-A1 NOVEL ALK2 INHIBITORS AND METHODS FOR INHIBITING BMP SIGNALING NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2023-01-05 US disclosed
US-20210238185-A1 CRYSTAL FORMS OF AN ALK2 INHIBITOR KEROS THERAPEUTICS, INC. 2021-08-05 US disclosed
US-11026947-B2 ALK2 inhibitors and methods for inhibiting BMP signaling THE BRIGHAM AND WOMEN'S HOSPITAL, INC. (US) 2021-06-08 US disclosed
US-10849871-B2 Compositions and methods of use of phorbol esters for the treatment of stroke BIOSUCCESS BIOTECH CO., LTD. (US) 2020-12-01 US disclosed
US-20200207697-A1 Compositions And Methods Of Use Of Phorbol Esters For Treatment of Stroke CHANG RICHARD L (US) 2020-07-02 US disclosed
US-20200179389-A1 NOVEL ALK2 INHIBITORS AND METHODS FOR INHIBITING BMP SIGNALING NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2020-06-11 US disclosed
US-20110039837-A1 OXADIAZOANTHRACENE COMPOUNDS FOR THE TREATMENT OF DIABETES TRANSTECH PHARMA, INC. (US) 2011-02-17 US disclosed
US-20100324033-A1 OXADIAZOANTHRACENE COMPOUNDS FOR THE TREATMENT OF DIABETES TRANSTECH PHARMA, INC. (US) 2010-12-23 US disclosed
EP-2262364-A2 OXADIAZOANTHRACENE COMPOUNDS FOR THE TREATMENT OF DIABETES TransTech Pharma, Inc (US) 2010-12-22 EP disclosed
WO-2010114824-A1 SUBSTITUTED AZOANTHRACENE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS, AND METHODS OF USE THEREOF TRANSTECH PHARMA INC (US) 2010-10-07 WO disclosed
US-7790714-B2 treating non-insulin dependent diabetes comprising administering a glucagon-like peptide receptor modulators such as (S)-2-({(S)-6-benzoyl-3-[4-(3,4-dichloro-benzyloxy)-phenyl]-2-oxo-2,3,5,6,7,8-hexahydro-1H-4-oxa-1,6-diaza-anthracene-7-carbonyl}-amino)-3-(4'-cyano-biphenyl-4-yl)-propionic acid TRANSTECH PHARMA, INC. (US) 2010-09-07 US disclosed
US-20100197677-A1 OXADIAZOANTHRACENE COMPOUNDS FOR THE TREATMENT OF DIABETES TRANSTECH PHARMA, INC. (US) 2010-08-05 US disclosed
US-7727983-B2 Glucagon-like peptide-1 (GLP-1) receptor modulators such as (S)-2-({(S)-6-Benzoyl-3-[4-(3,4-dichloro-benzyloxy)-phenyl]-2-oxo-2,3,5,6,7,8-hexahydro-1H-4-oxa-1,6-diaza-anthracene-7-carbonyl}-amino)-3-(4'-cyano-biphenyl-4-yl)-propionic acid, used as antidiabetic agents; bioavailability TRANSTECH PHARMA, INC. (US) 2010-06-01 US disclosed
US-20090306063-A1 Glucagon-like peptide-1 (GLP-1) receptor modulators such as (S)-2-({(S)-6-Benzoyl-3-[4-(3,4-dichloro-benzyloxy)-phenyl]-2-oxo-2,3,5,6,7,8-hexahydro-1H-4-oxa-1,6-diaza-anthracene-7-carbonyl}-amino)-3-(4'-cyano-biphenyl-4-yl)-propionic acid, used as antidiabetic agents; bioavailability TRANS TECH. PHARMA. INC. (US) 2009-12-10 US disclosed
WO-2009111700-A2 OXADIAZOANTHRACENE COMPOUNDS FOR THE TREATMENT OF DIABETES TRANSTECH PHARMA, INC. (US) 2009-09-11 WO disclosed
US-6927214-B1 Non-peptide GLP-1 agonists NOVO NORDISK A/S (DK) 2005-08-09 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 (11 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-10849871-B2 Compositions and methods of use of phorbol esters for the treatment of stroke PMAIP1, EBP, PLAT ADRB2 3887/4885ADRB1 3922/4885HTR1A 4409/4885
US-20200179389-A1 NOVEL ALK2 INHIBITORS AND METHODS FOR INHIBITING BMP SIGNALING BMPR2, BMP1, BMP2K ADRB2 3887/4885ADRB1 4353/4885HTR1A 3006/4885
US-20110039837-A1 OXADIAZOANTHRACENE COMPOUNDS FOR THE TREATMENT OF DIABETES GLP1R, GPR119, OTC ADRB2 115/4885ADRB1 56/4885HTR1A 2136/4885
US-20090306063-A1 Glucagon-like peptide-1 (GLP-1) receptor modulators such as (S)-2-({(S)-6-Benzoyl-3-[4-(3,4-dichloro-benzyloxy)-phenyl]-2-oxo-2,3,5,6,7,8-hexahydro-1H-4-oxa-1,6-diaza-anthracene-7-carbonyl}-amino)-3-(4'-cyano-biphenyl-4-yl)-propionic acid, used as antidiabetic agents; bioavailability GLP1R, GIPR, GCGR ADRB2 110/4885ADRB1 44/4885HTR1A 366/4885
US-20100197677-A1 OXADIAZOANTHRACENE COMPOUNDS FOR THE TREATMENT OF DIABETES GLP1R, GPR119, OTC ADRB2 115/4885ADRB1 56/4885HTR1A 2136/4885
US-20230000869-A1 NOVEL ALK2 INHIBITORS AND METHODS FOR INHIBITING BMP SIGNALING BMPR2, BMP1, BMP2K ADRB2 3887/4885ADRB1 4353/4885HTR1A 3006/4885
US-11654147-B2 ALK2 inhibitors and methods for inhibiting BMP signaling BMPR2, BMP1, BMP2K ADRB2 3645/4885ADRB1 4225/4885HTR1A 2955/4885
US-20100324033-A1 OXADIAZOANTHRACENE COMPOUNDS FOR THE TREATMENT OF DIABETES GLP1R, GPR119, OTC ADRB2 115/4885ADRB1 56/4885HTR1A 2136/4885
US-20200207697-A1 Compositions And Methods Of Use Of Phorbol Esters For Treatment of Stroke PMAIP1, PLAT, EBP ADRB2 3962/4885ADRB1 3990/4885HTR1A 4385/4885
US-11026947-B2 ALK2 inhibitors and methods for inhibiting BMP signaling BMPR2, BMP1, BMP2K ADRB2 3645/4885ADRB1 4225/4885HTR1A 2955/4885
US-20210238185-A1 CRYSTAL FORMS OF AN ALK2 INHIBITOR ALK, ALKBH3, ACVR2A ADRB2 1125/4885ADRB1 2253/4885HTR1A 3706/4885

“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.