Olodanrigan

Olodanrigan

SCHEMBL244657

COc1ccc2c(c1OCc1ccccc1)CC(C(=O)O)N(C(=O)C(c1ccccc1)c1ccccc1)C2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AGTR2

The experimentally established mechanism targets of Olodanrigan. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 2)

geneUniProtsupporting neighboursconfidence
AGTR2 known ✓ P50052 19/20 1.00
AGTR1 P30556 2/20 1.00

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
Olodanrigan SCHEMBL421411 1.00 AGTR2 (1.00) AGTR2AGTR1
Olodanrigan SCHEMBL8964136 1.00 AGTR2 (1.00) AGTR2AGTR1
Olodanrigan SCHEMBL29394365 1.00 AGTR2 (1.00) AGTR2AGTR1
SCHEMBL8964206 0.94 AGTR2 (1.00) AGTR2AGTR1
SCHEMBL3516607 0.94 AGTR2 (1.00) AGTR2AGTR1
SCHEMBL8964101 0.94 AGTR2 (1.00) AGTR2AGTR1
SCHEMBL3514261 0.94 AGTR2 (0.88) AGTR2AGTR1
SCHEMBL3519228 0.94 AGTR2 (1.00) AGTR2AGTR1
SCHEMBL3516610 0.94 AGTR2 (0.88) AGTR2AGTR1
SCHEMBL3517015 0.92 AGTR2 (0.87) AGTR2AGTR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160052925-A1 METHOD OF TREATMENT OR PROPHYLAXIS INFTAMMATORY PAIN NOVARTIS AG (CH) 2016-02-25 US claimed
EP-2525795-B1 METHODS AND COMPOSITIONS FOR IMPROVED NERVE CONDUCTION VELOCITY SPINIFEX PHARM PTY LTD (AU) 2015-10-21 EP claimed
US-9095587-B2 Methods and compositions for improved nerve conduction velocity SPINIFEX PHARMACEUTICALS PTY LTD (AU) 2015-08-04 US claimed
US-8551950-B2 Method of treatment or prophylaxis of inflammatory pain SPINIFEX PHARMACEUTICALS PTY LTD (AU) 2013-10-08 US claimed
US-20130131103-A1 Methods and Compositions For Improved Nerve Conduction Velocity NOVARTIS AG (CH) 2013-05-23 US claimed
US-8404686-B2 Method of treatment or prophylaxis SPINIFEX PHARMACEUTICALS PTY LTD (AU) 2013-03-26 US claimed
US-20120004259-A1 METHOD OF TREATMENT OR PROPHYLAXIS SPINIFEX PHARMACEUTICALS, PTY LTD (AU) 2012-01-05 US claimed
WO-2011088504-A1 METHODS AND COMPOSITIONS FOR IMPROVED NERVE CONDUCTION VELOCITY SPINIFEX PHARMACEUTICALS PTY LTD (AU) 2011-07-28 WO claimed
US-7795275-B2 Method of treatment or prophylaxis UNIQUEST PTY LIMITED (AU) 2010-09-14 US claimed
EP-0641326-A1 SUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINES WITH ANGIOTENSIN II RECEPTOR ANTAGONIST PROPERTIES WARNER-LAMBERT COMPANY (US) 1995-03-08 EP claimed
WO-1993023378-A1 SUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINES WITH ANGIOTENSIN II RECEPTOR ANTAGONIST PROPERTIES WARNER-LAMBERT COMPANY (US) 1993-11-25 WO claimed
US-5246943-A Substituted 1,2,3,4-tetahydroisoquinolines with angiotensin II receptor antagonist properties WARNER-LAMBERT COMPANY (US) 1993-09-21 US claimed
US-20230242522-A1 SALT OF TETRAHYDROISOQUINOLINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND MEDICAL USE THEREOF ZHEJIANG HISUN PHARMACEUTICAL CO., LTD. (CN) 2023-08-03 US disclosed
US-20230242522-A1 SALT OF TETRAHYDROISOQUINOLINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND MEDICAL USE THEREOF ZHEJIANG HISUN PHARMACEUTICAL CO., LTD. (CN) 2023-08-03 US disclosed
EP-4177253-A1 TETRAHYDROISOQUINOLINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND MEDICAL USE THEREOF Zhejiang Hisun Pharmaceutical Co., Ltd. (CN) 2023-05-10 EP disclosed
EP-4096648-A1 METHODS AND COMPOSITIONS FOR THE TREATMENT OF HEMANGIOMA Gillies Mcindoe Research Institute (NZ) 2022-12-07 EP disclosed
EP-0641326-A1 SUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINES WITH ANGIOTENSIN II RECEPTOR ANTAGONIST PROPERTIES WARNER-LAMBERT COMPANY (US) 1995-03-08 EP disclosed
US-5350757-A Treatment of vascular restenosis, nervous system disorders and cognition enhancement WARNER-LAMBERT COMPANY (US) 1994-09-27 US disclosed
WO-1993023378-A1 SUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINES WITH ANGIOTENSIN II RECEPTOR ANTAGONIST PROPERTIES WARNER-LAMBERT COMPANY (US) 1993-11-25 WO disclosed
US-5246943-A Substituted 1,2,3,4-tetahydroisoquinolines with angiotensin II receptor antagonist properties WARNER-LAMBERT COMPANY (US) 1993-09-21 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 (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-20130131103-A1 Methods and Compositions For Improved Nerve Conduction Velocity GAP43, CHRNB3, CHRNB4 AGTR2 6/4885AGTR1 7/4885
US-20230242522-A1 SALT OF TETRAHYDROISOQUINOLINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND MEDICAL USE THEREOF AGTR2, AGTR1, SLC5A11 AGTR2 1/4885AGTR1 2/4885
US-20160052925-A1 METHOD OF TREATMENT OR PROPHYLAXIS INFTAMMATORY PAIN AGTR2, AGTR1, BDKRB2 AGTR2 1/4885AGTR1 2/4885
US-20120004259-A1 METHOD OF TREATMENT OR PROPHYLAXIS AGTR2, AGTR1, NTSR2 AGTR2 1/4885AGTR1 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.