Ranolazine

Ranolazine

SCHEMBL611511

COc1ccccc1OCC(O)CN1CCN(CC(=O)Nc2c(C)cccc2C)CC1.[Cl-].[Cl-].[H+].[H+]

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SCN4ASCN5A

The experimentally established mechanism targets of Ranolazine. 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
SCN5A known ✓ Q14524 1/20 0.96
CYP3A4 P08684 2/20 0.96
CYP2D6 P10635 1/20 0.96
TSHR P16473 1/20 0.96
NFKB1 P19838 1/20 0.96
ADRB2 P07550 1/20 0.96
ADRB1 P08588 1/20 0.96
ADRA2A P08913 1/20 0.96
ADRA2B P18089 1/20 0.96
ADRA2C P18825 1/20 0.96
ADRA1A P35348 1/20 0.96
DRD3 P35462 1/20 0.96
HTR2B P41595 1/20 0.96
KCNH2 Q12809 1/20 0.96
LMNA P02545 3/20 0.94
BLM P54132 1/20 0.94
PMP22 Q01453 1/20 0.94
NPSR1 Q6W5P4 1/20 0.94
MEN1 O00255 1/20 0.57
KMT2A Q03164 1/20 0.57

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
Ranolazine SCHEMBL1495098 0.98 CYP3A4 (1.00) CYP3A4CYP2D6TSHRNFKB1ADRB2
Ranolazine SCHEMBL1534086 0.98 CYP3A4 (1.00) CYP3A4CYP2D6TSHRNFKB1ADRB2
Ranolazine SCHEMBL124666 0.98 CYP3A4 (1.00) CYP3A4CYP2D6TSHRNFKB1ADRB2
Ranolazine SCHEMBL30296819 0.98 CYP3A4 (1.00) CYP3A4CYP2D6TSHRNFKB1ADRB2
Ranolazine SCHEMBL7933344 0.98 CYP3A4 (1.00) CYP3A4CYP2D6TSHRNFKB1ADRB2
Ranolazine SCHEMBL124665 0.98 CYP3A4 (1.00) CYP3A4CYP2D6TSHRNFKB1ADRB2
Ranolazine SCHEMBL6391141 0.98 CYP3A4 (1.00) CYP3A4CYP2D6TSHRNFKB1ADRB2
Ranolazine SCHEMBL14841986 0.97 CYP3A4 (0.98) CYP3A4CYP2D6TSHRNFKB1ADRB2
Ranolazine SCHEMBL612077 0.97 LMNA (1.00) CYP3A4CYP2D6TSHRNFKB1ADRB2
Ranolazine SCHEMBL230758 0.97 LMNA (1.00) CYP3A4CYP2D6TSHRNFKB1ADRB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3004138-B1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME BAUSCH HEALTH IRELAND LTD (IE) 2024-03-13 EP disclosed
EP-4309673-A2 FORMULATIONS OF GUANYLATE CYCLASE C AGONISTS AND METHODS OF USE Bausch Health Ireland Limited (IE) 2024-01-24 EP disclosed
US-20240002440-A1 AGONISTS OF GUANYLATE CYCLASE USEFUL FOR THE TREATMENT OF GASTROINTESTINAL DISORDERS, INFLAMMATION, CANCER AND OTHER DISORDERS JPMORGAN CHASE BANK, N.A. 2024-01-04 US disclosed
US-11834521-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same BAUSCH HEALTH IRELAND LIMITED (IE) 2023-12-05 US disclosed
US-20230340023-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME JPMORGAN CHASE BANK, N.A. 2023-10-26 US disclosed
EP-3708179-B1 FORMULATIONS OF GUANYLATE CYCLASE C AGONISTS AND METHODS OF USE BAUSCH HEALTH IRELAND LTD (IE) 2023-10-04 EP disclosed
CN-114441663-A Method for screening protein positive compounds by using solid phase microextraction affinity selection mass spectrum 中国科学院上海药物研究所 2022-05-06 CN disclosed
US-11319346-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same BAUSCH HEALTH IRELAND LIMITED (IE) 2022-05-03 US disclosed
US-20220119449-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME BAUSCH HEALTH IRELAND LIMITED (IE) 2022-04-21 US disclosed
US-20210403508-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME JPMORGAN CHASE BANK, N.A. 2021-12-30 US disclosed
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 disclosed
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 disclosed
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 disclosed
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 disclosed
US-6190691-B1 ADMINISTERING FORMULATION COMPRISING TUMOR NERCOSIS FACTOR (TNF) PRODUCTION-INHIBITORY AMOUNT OF A COMPOUND SELECTED FROM LOPERAMIDE AND DIPHENOXYLATE TO MAMMAL ADOLOR CORPORATION 2001-02-20 US disclosed
US-5962477-A USING LOPERAMIDE ADOLOR CORPORATION (US) 1999-10-05 US disclosed
EP-0937460-A2 Use of an antidiarrheal for the manufacture of a medicament for the treatment of inflammatory conditions Adolor Corporation (US) 1999-08-25 EP disclosed
EP-0757558-A4 SCREENING METHODS FOR INTEGUMENTAL INFLAMMATION MODULATING AGENTS ALZA CORP (US) 1999-06-16 EP disclosed
EP-0757558-A1 SCREENING METHODS FOR INTEGUMENTAL INFLAMMATION MODULATING AGENTS ALZA CORPORATION (US) 1997-02-12 EP disclosed
WO-1995027510-A1 SCREENING METHODS FOR INTEGUMENTAL INFLAMMATION MODULATING AGENTS ALZA CORPORATION (US) 1995-10-19 WO 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 (6 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-20230340023-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME GUCY1A1, GUCY1A2, GUCY1B1 SCN5A 826/4885CYP3A4 2583/4885CYP2D6 3754/4885
US-20210403508-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME GUCY1A1, GUCY1A2, GUCY1B1 SCN5A 826/4885CYP3A4 2583/4885CYP2D6 3754/4885
US-20030069221-A1 Combinations of sterol absorption inhibitor(s) with cardiovascular agent(s) for the treatment of vascular conditions CYP46A1, FABP2, SREBF1 SCN5A 2330/4885CYP3A4 464/4885CYP2D6 1549/4885
US-20220119449-A1 ULTRA-PURE AGONISTS OF GUANYLATE CYCLASE C, METHOD OF MAKING AND USING SAME GUCY1A1, GUCY1A2, GUCY1B1 SCN5A 826/4885CYP3A4 2583/4885CYP2D6 3754/4885
US-11319346-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same GUCY1A1, GUCY1A2, GUCY1B1 SCN5A 826/4885CYP3A4 2583/4885CYP2D6 3754/4885
US-11834521-B2 Ultra-pure agonists of guanylate cyclase C, method of making and using same GUCY1A1, GUCY1A2, GUCY1B1 SCN5A 826/4885CYP3A4 2583/4885CYP2D6 3754/4885

“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.