Pinacidil Anhydrous

Pinacidil Anhydrous

SCHEMBL1650693

CC(N=C(NC#N)Nc1ccncc1)C(C)(C)C.O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9KCNJ11

The experimentally established mechanism targets of Pinacidil Anhydrous. 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
ABCC9 known ✓ O60706 8/20 1.00
KCNJ11 known ✓ Q14654 8/20 1.00
CYP3A4 P08684 3/20 1.00
CYP1A2 P05177 2/20 1.00
CYP2C9 P11712 1/20 1.00
ALOX15 P16050 1/20 1.00
NFKB1 P19838 1/20 1.00
MAPK1 P28482 1/20 1.00
CYP2C19 P33261 1/20 1.00
HIF1A Q16665 1/20 1.00
HSD17B10 Q99714 1/20 1.00
ALDH1A1 P00352 1/20 1.00
LMNA P02545 1/20 1.00
GLA P06280 1/20 1.00
BLM P54132 1/20 1.00
PMP22 Q01453 1/20 1.00
NPSR1 Q6W5P4 1/20 1.00
NAMPT P43490 9/20 0.47
P2RX7 Q99572 1/20 0.45
ABCC8 Q09428 2/20 0.44

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
(R)-Pinacidil SCHEMBL29484626 1.00 ABCC9 (1.00) ABCC9KCNJ11CYP3A4CYP1A2CYP2C9
Pinacidil Anhydrous SCHEMBL9260276 1.00 ABCC9 (1.00) ABCC9KCNJ11CYP3A4CYP1A2CYP2C9
Pinacidil Anhydrous SCHEMBL9351684 1.00 ABCC9 (1.00) ABCC9KCNJ11CYP3A4CYP1A2CYP2C9
Pinacidil Anhydrous SCHEMBL65787 1.00 ABCC9 (1.00) ABCC9KCNJ11CYP3A4CYP1A2CYP2C9
SCHEMBL9456841 0.84 ABCC9 (0.73) ABCC9KCNJ11CYP3A4CYP1A2CYP2C9
SCHEMBL9298614 0.84 KCNJ11 (0.72) ABCC9KCNJ11CYP3A4CYP1A2CYP2C9
SCHEMBL9298619 0.84 KCNJ11 (0.72) ABCC9KCNJ11CYP3A4CYP1A2CYP2C9
Naminidil SCHEMBL1650535 0.83 ABCC9 (1.00) ABCC9KCNJ11CYP3A4CYP1A2CYP2C9
Naminidil SCHEMBL6375460 0.83 ABCC9 (1.00) ABCC9KCNJ11CYP3A4CYP1A2CYP2C9
SCHEMBL6369125 0.81 ABCC9 (0.68) ABCC9KCNJ11CYP3A4CYP1A2CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0306192-B1 PERMEATION ENHANCEMENT COMPOSITIONS ELI LILLY AND COMPANY (US) 1992-05-27 EP claimed
EP-2576778-B1 TRANSGENIC REPORTER SYSTEM THAT REVEALS EXPRESSION PROFILES AND REGULATION MECHANISMS OF ALTERNATIVE SPLICING IN RODENTS UNIV KYOTO (JP) 2017-08-09 EP disclosed
US-9273364-B2 Transgenic reporter system that reveals expression profiles and regulation mechanisms of alternative splicing in mammalian organisms KYOTO UNIVERSITY (JP) 2016-03-01 US disclosed
US-20130137099-A1 TRANSGENIC REPORTER SYSTEM THAT REVEALS EXPRESSION PROFILES AND REGULATION MECHANISMS OF ALTERNATIVE SPLICING IN MAMMALIAN ORGANISMS KYOTO UNIVERSITY (JP) 2013-05-30 US disclosed
US-7927613-B2 Pharmaceutical co-crystal compositions UNIVERSITY OF SOUTH FLORIDA (US) 2011-04-19 US disclosed
US-7790905-B2 Pharmaceutical propylene glycol solvate compositions MCNEIL-PPC, INC. (US) 2010-09-07 US disclosed
US-20100113379-A1 cAMP DEPENDENT INDUCTION OF AUTOPHAGY RUBINSZTEIN DAVID 2010-05-06 US disclosed
US-20090012067-A1 Modulation of Hypothalamic Atp-Sensitive Potassium Channels ALBERT EINSTEIN COLLEGE OF MEDICINE, INC. 2009-01-08 US disclosed
WO-2008099175-A1 CAMP DEPENDENT INDUCTION OF AUTOPHAGY CAMBRIDGE ENTERPRISE LIMITED (GB) 2008-08-21 WO disclosed
US-20070026079-A1 Intranasal administration of modulators of hypothalamic ATP-sensitive potassium channels DARA BIOSCIENCES, INC. 2007-02-01 US disclosed
US-5532248-A O-aryl,O-alkyl, and O-alkenyl-macrolides having immunosuppressive activity MERCK CO., INC. (US) 1996-07-02 US disclosed
EP-0542802-B1 STIMULATION OF HAIR GROWTH WITH POTASSIUM CHANNEL OPENERS AND 5-ALPHA-REDUCTASE INHIBITORS UPJOHN CO (US) 1996-03-06 EP disclosed
WO-1995009857-A1 O-ARYL, O-ALKYL, O-ALKENYL AND O-ALKYNYL-MACROLIDES HAVING IMMUNOSUPPRESSIVE ACTIVITY MERCK & CO., INC. (US) 1995-04-13 WO disclosed
US-5349061-A O-heteroaryl, O-alkylheteroaryl, O-alkenylheteroaryl and O-alkynylheteroarylmacrolides having immunosuppressive activity MERCK & CO., INC. (US) 1994-09-20 US disclosed
EP-0405525-B1 Novel cyanoguanidine derivatives KANEBO LTD (JP) 1994-09-14 EP disclosed
US-5344925-A Autoimmune diseases; infections; organ transplants MERCK & CO., INC. (US) 1994-09-06 US disclosed
WO-1992009259-A1 STIMULATION OF HAIR GROWTH WITH POTASSIUM CHANNEL OPENERS AND AN ANDROGEN RECEPTOR BLOCKER THE UPJOHN COMPANY (US) 1992-06-11 WO disclosed
US-5087640-A Potassium channel openers; hypotensive agents, coronary vasodilators KANEBO, LTD. (JP) 1992-02-11 US disclosed
EP-0207606-A2 Use of pinacidil as an antiasthma agent ELI LILLY AND COMPANY (US) 1987-01-07 EP disclosed
US-4617311-A ADMINISTERING PINACIDIL ELI LILLY AND COMPANY (US) 1986-10-14 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 (3 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-20090012067-A1 Modulation of Hypothalamic Atp-Sensitive Potassium Channels PYGB, PC, KCNN3 ABCC9 384/4885KCNJ11 18/4885CYP3A4 2037/4885
US-20070026079-A1 Intranasal administration of modulators of hypothalamic ATP-sensitive potassium channels PC, LIPE, ATP5ME ABCC9 482/4885KCNJ11 24/4885CYP3A4 3579/4885
US-20100113379-A1 cAMP DEPENDENT INDUCTION OF AUTOPHAGY ATF4, TFEB, BECN1 ABCC9 3634/4885KCNJ11 4444/4885CYP3A4 4671/4885

“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.