Mesudipine

Mesudipine

SCHEMBL1900480

CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1c1cccnc1SC

nearest known ligand 0.60

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 5/20 0.60
HSD17B10 Q99714 3/20 0.60
CASP1 P29466 1/20 0.60
CACNA1C Q13936 3/20 0.56
ALDH1A1 P00352 3/20 0.54
CYP2C9 P11712 4/20 0.52
CYP3A4 P08684 3/20 0.52
CYP2C19 P33261 3/20 0.52
ADORA3 P0DMS8 3/20 0.52
MEN1 O00255 2/20 0.52
CYP1A2 P05177 2/20 0.52
KMT2A Q03164 2/20 0.52
HIF1A Q16665 2/20 0.52
GAA P10253 2/20 0.52
TSHR P16473 2/20 0.52
NR1I2 O75469 2/20 0.52
LMNA P02545 2/20 0.52
PGR P06401 2/20 0.52
OPRK1 P41145 2/20 0.52
PDE4D Q08499 2/20 0.52

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
SCHEMBL9765753 0.95 KDM4E (0.56) KDM4EHSD17B10CASP1CACNA1CALDH1A1
SCHEMBL9765777 0.95 KDM4E (0.59) KDM4EHSD17B10CASP1CACNA1CALDH1A1
SCHEMBL7430107 0.91 KDM4E (0.51) KDM4EHSD17B10CASP1CACNA1CALDH1A1
SCHEMBL10555153 0.81 KDM4E (0.64) KDM4EHSD17B10CASP1CACNA1CALDH1A1
SCHEMBL11364576 0.80 KDM4E (0.41) KDM4EHSD17B10CASP1CACNA1CALDH1A1
SCHEMBL11356558 0.80 KDM4E (0.41) KDM4EHSD17B10CASP1CACNA1CALDH1A1
SCHEMBL9833019 0.80 CACNA1C (0.64) KDM4EHSD17B10CASP1CACNA1CALDH1A1
SCHEMBL9765762 0.79 KDM4E (0.68) KDM4EHSD17B10CASP1CACNA1CALDH1A1
SCHEMBL27676982 0.76 KDM4E (0.58) KDM4EHSD17B10CASP1CACNA1CALDH1A1
SCHEMBL9835820 0.76 CA1 (0.64) KDM4EHSD17B10CASP1CACNA1CALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9016221-B2 Surface topographies for non-toxic bioadhesion control UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC. (US) 2015-04-28 US claimed
WO-2011060944-A2 ACTIVE PHARMACEUTICAL INGREDIENT CAPSULES AND POLYUNSATURATED FATTY ACID ESTERS GP PHARM, S.A. (ES) 2011-05-26 WO claimed
US-20100226943-A1 SURFACE TOPOGRAPHIES FOR NON-TOXIC BIOADHESION CONTROL UNIVERSITY OF FLORIDA (US) 2010-09-09 US claimed
CN-101330905-A Freeze-drying process and products obtained thereby SCIDOSE LLC (US) 2008-12-24 CN claimed
EP-1954244-A1 LYOPHILIZATION PROCESS AND PRODUCTS OBTAINED THEREBY Scidose, Llc (US) 2008-08-13 EP claimed
WO-2007061529-A1 LYOPHILIZATION PROCESS AND PRODUCTS OBTAINED THEREBY SCIDOSE LLC. (US) 2007-05-31 WO claimed
US-20070116729-A1 Lyophilization process and products obtained thereby SCIDOSE LLC 2007-05-24 US claimed
EP-0639986-A1 TOPICAL OPHTHALMIC COMPOSITIONS COMPRISING A COMBINATION OF CALCIUM ANTAGONISTS WITH KNOWN ANTIGLAUCOMA AGENTS ALCON LABORATORIES, INC. (US) 1995-03-01 EP claimed
WO-1993023082-A1 TOPICAL OPHTHALMIC COMPOSITIONS COMPRISING A COMBINATION OF CALCIUM ANTAGONISTS WITH KNOWN ANTIGLAUCOMA AGENTS ALCON LABORATORIES, INC. (US) 1993-11-25 WO claimed
EP-0301133-A2 Long acting formulation SYNTEX (U.S.A.) INC. (US) 1989-02-01 EP claimed
EP-3485881-B1 PERMANENTLY CHARGED SODIUM AND CALCIUM CHANNEL BLOCKERS AS ANTI-INFLAMMATORY AGENTS HARVARD COLLEGE (US) 2024-03-13 EP disclosed
US-20230241047-A1 TREATMENT FOR DOPAMINERGIC DISORDERS NORTHWESTERN UNIVERSITY 2023-08-03 US disclosed
US-20230165812-A1 NOCICEPTOR NEURONS CONTROL CANCER IMMUNOSURVEILLANCE PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2023-06-01 US disclosed
US-20220304994-A1 TREATMENT FOR DOPAMINERGIC DISORDERS NORTHWESTERN UNIVERSITY 2022-09-29 US disclosed
US-20220047505-A1 Controlled Absorption Water-Soluble Pharmaceutically Active Organic Compound Formulation for Once-Daily Administration STI PHARMA, LLC (US) 2022-02-17 US disclosed
WO-1990010005-A1 PYRIDYLCARBOXYL-ISOSORBIDE DERIVATIVE, MANUFACTURING PROCESS AND USES HEINRICH MACK NACHF. (DE) 1990-09-07 WO disclosed
EP-0385348-A1 Pyridylcarboxyl-isosorbide derivative, manufacturing process and uses Heinrich Mack Nachf. (DE) 1990-09-05 EP disclosed
US-4940556-A SUSTAINED RELEASE OF CALCIUM CHANNEL BLOCKERS SYNTEX (U.S.A.) INC. (US) 1990-07-10 US disclosed
US-4885305-A ADMINISTERING NICARDIPINE OR ITS HYDROCHLORIDE SALT YAMANOUCHI PHARMACEUTICAL CO., LTD. (JP) 1989-12-05 US disclosed
EP-0301133-A2 Long acting formulation SYNTEX (U.S.A.) INC. (US) 1989-02-01 EP 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-20230165812-A1 NOCICEPTOR NEURONS CONTROL CANCER IMMUNOSURVEILLANCE OPRL1, MRGPRX1, RAMP1 KDM4E 3030/4885HSD17B10 4639/4885CASP1 375/4885

“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.