Isonipecotic Acid

Isonipecotic Acid

SCHEMBL2027408

O=C(O)C1CCNCC1.O=C(O)C1CCNCC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 3/20 1.00
▸ GABRA1 P14867 2/20 1.00
▸ GABRG2 P18507 2/20 1.00
▸ GABRB3 P28472 2/20 1.00
▸ GABRA5 P31644 2/20 1.00
▸ GABRA3 P34903 2/20 1.00
▸ GABRA2 P47869 2/20 1.00
▸ GABRA6 Q16445 2/20 1.00
▸ GABRP O00591 1/20 1.00
▸ GABRD O14764 1/20 1.00
▸ GABRB1 P18505 1/20 1.00
▸ GABRB2 P47870 1/20 1.00
▸ GABRA4 P48169 1/20 1.00
▸ GABRE P78334 1/20 1.00
▸ PMP22 Q01453 1/20 1.00
▸ GABRG1 Q8N1C3 1/20 1.00
▸ GABRG3 Q99928 1/20 1.00
▸ GABRQ Q9UN88 1/20 1.00
▸ LMNA P02545 3/20 0.52
▸ SLC6A1 P30531 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
Isonipecotic Acid SCHEMBL104297 1.00 — —
Isonipecotic Acid SCHEMBL5035880 0.97 TSHR (0.94) TSHRGABRA1GABRG2GABRB3GABRA5
Isonipecotic Acid SCHEMBL30060745 0.97 TSHR (0.94) TSHRGABRA1GABRG2GABRB3GABRA5
Isonipecotic Acid SCHEMBL11556866 0.97 TSHR (0.94) TSHRGABRA1GABRG2GABRB3GABRA5
Isonipecotic Acid SCHEMBL6122239 0.97 TSHR (0.94) TSHRGABRA1GABRG2GABRB3GABRA5
Isonipecotic Acid SCHEMBL23043998 0.97 TSHR (0.94) TSHRGABRA1GABRG2GABRB3GABRA5
Isonipecotic Acid SCHEMBL2560208 0.97 TSHR (0.94) TSHRGABRA1GABRG2GABRB3GABRA5
Isonipecotic Acid SCHEMBL31602943 0.97 TSHR (0.94) TSHRGABRA1GABRG2GABRB3GABRA5
Isonipecotic Acid SCHEMBL1703706 0.97 TSHR (0.94) TSHRGABRA1GABRG2GABRB3GABRA5
Isonipecotic Acid SCHEMBL28089924 0.97 TSHR (0.94) TSHRGABRA1GABRG2GABRB3GABRA5

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 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10017481-B2 Conformationally constrained, fully synthetic macrocyclic compounds POLYPHOR AG (CH) 2018-07-10 — — US claimed
EP-2836485-B1 CONFORMATIONALLY CONSTRAINED, FULLY SYNTHETIC MACROCYCLIC COMPOUNDS POLYPHOR AG (CH) 2018-01-10 — — EP claimed
US-20150051183-A1 CONFORMATIONALLY CONSTRAINED, FULLY SYNTHETIC MACROCYCLIC COMPOUNDS POLYPHOR AG (CH) 2015-02-19 — — US claimed
EP-2836485-A1 CONFORMATIONALLY CONSTRAINED, FULLY SYNTHETIC MACROCYCLIC COMPOUNDS Polyphor Ag (CH) 2015-02-18 — — EP claimed
WO-2013139697-A1 CONFORMATIONALLY CONSTRAINED, FULLY SYNTHETIC MACROCYCLIC COMPOUNDS POLYPHOR AG (CH) 2013-09-26 — — WO claimed
US-10017481-B2 Conformationally constrained, fully synthetic macrocyclic compounds POLYPHOR AG (CH) 2018-07-10 — — US disclosed
EP-2836485-B1 CONFORMATIONALLY CONSTRAINED, FULLY SYNTHETIC MACROCYCLIC COMPOUNDS POLYPHOR AG (CH) 2018-01-10 — — EP disclosed
EP-3158053-A1 ACCELERATION OF MYCOBACTERIUM GROWTH St. George's Hospital Medical School (GB) 2017-04-26 — — EP disclosed
WO-2015193688-A1 ACCELERATION OF MYCOBACTERIUM GROWTH ST GEORGE'S HOSPITAL MEDICAL SCHOOL (GB) 2015-12-23 — — WO disclosed
US-20150051183-A1 CONFORMATIONALLY CONSTRAINED, FULLY SYNTHETIC MACROCYCLIC COMPOUNDS POLYPHOR AG (CH) 2015-02-19 — — US disclosed
EP-2836485-A1 CONFORMATIONALLY CONSTRAINED, FULLY SYNTHETIC MACROCYCLIC COMPOUNDS Polyphor Ag (CH) 2015-02-18 — — EP disclosed
WO-2013139697-A1 CONFORMATIONALLY CONSTRAINED, FULLY SYNTHETIC MACROCYCLIC COMPOUNDS POLYPHOR AG (CH) 2013-09-26 — — WO disclosed
WO-2011123654-A1 COMPOSITIONS AND METHODS OF SYNTHESIS OF PYRIDINOYLPIPERIDINE 5-HT1F AGONISTS COLUCID PHARMACEUTICALS, INC. (US) 2011-10-06 — — WO disclosed
US-20110236429-A1 Small Cationic Antimicrobial Peptides THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2011-09-29 — — US disclosed
US-20110195238-A1 ANTHRAPYRIDONE COLORING MATTER, SALT THEREOF, INK COMPOSITION AND COLORED BODY NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2011-08-11 — — US disclosed
US-20110150917-A1 Small Cationic Antimicrobial Peptides THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2011-06-23 — — US disclosed
WO-2008151434-A1 SMALL CATIONIC ANTIMICROBIAL PEPTIDES THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2008-12-18 — — 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 (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-20110195238-A1 ANTHRAPYRIDONE COLORING MATTER, SALT THEREOF, INK COMPOSITION AND COLORED BODY XDH, HAX1, ANXA1 TSHR 3438/4885GABRA1 4292/4885GABRG2 4554/4885
US-10017481-B2 Conformationally constrained, fully synthetic macrocyclic compounds CTSE, CTSB, CTSS TSHR 28/4885GABRA1 916/4885GABRG2 1444/4885
US-20150051183-A1 CONFORMATIONALLY CONSTRAINED, FULLY SYNTHETIC MACROCYCLIC COMPOUNDS CTSE, CTSB, CTSS TSHR 28/4885GABRA1 916/4885GABRG2 1444/4885

“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.

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