Niguldipine

Niguldipine

SCHEMBL245993

COC(=O)C1=C(C)NC(C)=C(C(=O)OCCCN2CCC(c3ccccc3)(c3ccccc3)CC2)C1c1cccc([N+](=O)[O-])c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADRA1A P35348 9/20 1.00
ADRA2A P08913 8/20 1.00
ADRA2B P18089 8/20 1.00
ADRA2C P18825 8/20 1.00
ADRA1D P25100 8/20 1.00
ADRA1B P35368 8/20 1.00
MAPT P10636 5/20 1.00
TDP1 Q9NUW8 4/20 1.00
MEN1 O00255 4/20 1.00
KMT2A Q03164 4/20 1.00
CYP1A2 P05177 3/20 1.00
CYP3A4 P08684 3/20 1.00
CYP2C9 P11712 3/20 1.00
CYP2C19 P33261 3/20 1.00
ABCB1 P08183 2/20 1.00
ADORA3 P0DMS8 2/20 1.00
CYP2D6 P10635 2/20 1.00
TP53 P04637 1/20 1.00
CHRM2 P08172 1/20 1.00
HTR1A P08908 1/20 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
Niguldipine SCHEMBL245992 1.00 ADRA1A (1.00) ADRA1AADRA2AADRA2BADRA2CADRA1D
Dexniguldipine SCHEMBL29615752 1.00 ADRA1A (1.00) ADRA1AADRA2AADRA2BADRA2CADRA1D
Dexniguldipine SCHEMBL724137 1.00 ADRA1A (1.00) ADRA1AADRA2AADRA2BADRA2CADRA1D
Niguldipine SCHEMBL29385244 1.00 ADRA1A (1.00) ADRA1AADRA2AADRA2BADRA2CADRA1D
Niguldipine SCHEMBL29386264 1.00 ADRA1A (1.00) ADRA1AADRA2AADRA2BADRA2CADRA1D
Niguldipine SCHEMBL3869443 0.99 ADRA1A (0.98) ADRA1AADRA2AADRA2BADRA2CADRA1D
Niguldipine SCHEMBL9001404 0.99 ADRA1A (1.00) ADRA1AADRA2AADRA2BADRA2CADRA1D
Niguldipine SCHEMBL467245 0.99 ADRA1A (1.00) ADRA1AADRA2AADRA2BADRA2CADRA1D
Dexniguldipine SCHEMBL1228966 0.99 ADRA1A (1.00) ADRA1AADRA2AADRA2BADRA2CADRA1D
SCHEMBL9386117 0.98 ADRA1A (0.95) ADRA1AADRA2AADRA2BADRA2CADRA1D

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 1967 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025229029-A1 CONJUGATE OF A SENOTHERAPEUTIC MOIETY AND A LIPID-TARGETING MOIETY GORGOULIS VASSILIS G (GR) 2025-11-06 WO claimed
US-20250213647-A1 CHEMOKINE RECEPTORS AND ALPHA1 ADRENERGIC RECEPTORS/VASOPRESSIN RECEPTORS 1A HETEROMERS AS DRUG TARGETS FOR DISEASE UNIVERSITY OF SOUTH FLORIDA 2025-07-03 US claimed
US-20250186415-A1 EXTENDED-RELEASE PHARMACEUTICAL COMPOSITIONS FOR TREATING EYE CONDITIONS FIFTH THIRD BANK, NATIONAL ASSOCIATION, AS AGENT 2025-06-12 US claimed
WO-2025034510-A1 ADRENERGIC ANTAGONISTS FOR USE IN A METHOD FOR TREATING CEREBRAL EDEMA OR A BRAIN INJURY UNIVERSITY OF ROCHESTER (US) 2025-02-13 WO claimed
EP-4489858-A1 EXTENDED-RELEASE PHARMACEUTICAL COMPOSITIONS FOR TREATING EYE CONDITIONS Harrow IP, LLC (US) 2025-01-15 EP claimed
US-20230330188-A1 PHARMACEUTICAL COMBINATION FOR USE IN THE TREATMENT AND/OR PREVENTION OF DIABETES INSPHERO AG (CH) 2023-10-19 US claimed
WO-2023192319-A1 CHEMOKINE RECEPTORS AND ALPHA1 ADRENERGIC RECEPTORS/VASOPRESSIN RECEPTORS 1A HETEROMERS AS DRUG TARGETS FOR DISEASE UNIVERSITY OF SOUTH FLORIDA (US) 2023-10-05 WO claimed
WO-2023172240-A1 EXTENDED-RELEASE PHARMACEUTICAL COMPOSITIONS FOR TREATING EYE CONDITIONS HARROW IP, LLC (US) 2023-09-14 WO claimed
EP-4225296-A1 PHARMACEUTICAL COMBINATION FOR USE IN THE TREATMENT AND/OR PREVENTION OF DIABETES Insphero AG (CH) 2023-08-16 EP claimed
US-20220387408-A1 USE OF MAST CELL STABILIZER FOR THE TREATMENT OF HEART FAILURE WITH PRESERVED EJECTION FRACTION INST NAT SANTE RECH MED (FR) 2022-12-08 US claimed
EP-1059912-A2 USE OF A COMPOUND INHIBITING THE ACTIVITY OF A SODIUM CHANNEL AND A CALCIUM CHANNEL IN A COMPOSITION FOR TOPICAL USE L'OREAL (FR) 2000-12-20 EP claimed
WO-2000012075-A1 NITROSATED AND NITROSYLATED ALPHA-ADRENERGIC RECEPTOR ANTAGONISTS, COMPOSITIONS AND METHODS OF USE NITROMED, INC. (US) 2000-03-09 WO claimed
WO-2000002543-A2 ANTIHYPERSENSITIVE COMBINATION OF VALSARTAN AND CALCIUM CHANNEL BLOCKER NOVARTIS AG (CH) 2000-01-20 WO claimed
WO-1999044579-A2 USE OF A COMPOUND INHIBITING THE ACTIVITY OF A SODIUM CHANNEL AND A CALCIUM CHANNEL IN A COMPOSITION FOR TOPICAL USE L'OREAL (FR) 1999-09-10 WO claimed
WO-1997038693-A1 CALCIUM CHANNEL BLOCKERS AS HUMAN CONJUNCTIVAL MAST CELL DEGRANULATION INHIBITORS FOR TREATING OCULAR ALLERGIC CONDITIONS ALCON LABORATORIES, INC. (US) 1997-10-23 WO claimed
EP-0176956-B1 Diaryl derivatives BYK GULDEN LOMBERG CHEM FAB (DE) 1994-06-15 EP claimed
EP-0584250-A4 1994-03-30 EP claimed
EP-0584250-A1 NOVEL COMPOSITION OF ANGIOTENSIN-II RECEPTOR ANTAGONISTS AND CALCIUM CHANNEL BLOCKERS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1994-03-02 EP claimed
WO-1992020342-A1 NOVEL COMPOSITION OF ANGIOTENSIN-II RECEPTOR ANTAGONISTS AND CALCIUM CHANNEL BLOCKERS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1992-11-26 WO claimed
US-4707486-A Diaryl piperidine containing esters of 1,4-dihydropyridines and coronary therapeutic use BYK GULDEN LOMBERG CHEMISCHE FABRIK GMBH (DE) 1987-11-17 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 (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-20230330188-A1 PHARMACEUTICAL COMBINATION FOR USE IN THE TREATMENT AND/OR PREVENTION OF DIABETES IAPP, SLC5A2, GLP1R ADRA1A 508/4885ADRA2A 351/4885ADRA2B 254/4885

“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.