SCHEMBL519750

SCHEMBL519750

CN(C)S(=O)(=O)c1cccc(N)c1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 1/20 0.61
▸ CA2 P00918 4/20 0.59
▸ CA12 O43570 3/20 0.59
▸ CA1 P00915 3/20 0.59
▸ CA9 Q16790 3/20 0.59
▸ CA4 P22748 2/20 0.59
▸ CA14 Q9ULX7 1/20 0.59
▸ ALDH1A1 P00352 3/20 0.57
▸ TSHR P16473 1/20 0.57
▸ HSD17B10 Q99714 1/20 0.57
▸ TDP1 Q9NUW8 1/20 0.57
▸ RAB9A P51151 3/20 0.54
▸ NPC1 O15118 2/20 0.54
▸ TNF P01375 1/20 0.54
▸ NOD1 Q9Y239 1/20 0.54
▸ MEN1 O00255 3/20 0.49
▸ KMT2A Q03164 3/20 0.49
▸ F2 P00734 3/20 0.49
▸ PRSS1 P07477 3/20 0.49
▸ PRSS2 P07478 3/20 0.49

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
SCHEMBL7163455 0.85 RAB9A (0.63) LMNACA2CA1ALDH1A1TSHR
SCHEMBL10860489 0.83 LMNA (0.55) LMNACA2CA12CA1CA9
SCHEMBL4070721 0.83 LMNA (0.55) LMNACA2CA12CA1CA9
SCHEMBL8251507 0.82 LMNA (0.53) LMNACA2CA12CA1CA9
SCHEMBL11307758 0.80 LMNA (0.57) LMNACA2CA12CA1CA9
SCHEMBL5880397 0.80 CA2 (0.68) CA2CA12CA1CA9CA4
SCHEMBL31055696 0.80 CA2 (0.68) CA2CA12CA1CA9CA4
SCHEMBL29405930 0.79 ALDH1A1 (0.69) LMNACA2CA12CA1CA9
SCHEMBL2481197 0.79 ALDH1A1 (0.54) LMNAALDH1A1TDP1RAB9ANPC1
SCHEMBL2480051 0.79 ALDH1A1 (0.69) LMNACA2CA12CA1CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1451160-B1 PYRAZOLE-AMIDES FOR USE IN THE TREATMENT OF PAIN ICAGEN INC (US) 2010-01-13 — — EP claimed
EP-1761541-B1 PYRRAZOLO-PYRIMIDINE DERIVATIVES HOFFMANN LA ROCHE (CH) 2008-01-09 — — EP claimed
EP-1761541-A1 PYRRAZOLO-PYRIMIDINE DERIVATIVES F.HOFFMANN-LA ROCHE AG (CH) 2007-03-14 — — EP claimed
WO-2005123738-A1 PYRRAZOLO-PYRIMIDINE DERIVATIVES F.HOFFMANN-LA ROCHE AG (CH) 2005-12-29 — — WO claimed
EP-4719385-A2 1H-PYRAZOLO[3,4-D]PYRIMIDIN-4-AMINES AS ANTI-INFECTIOUS AGENTS University of Vermont and State Agricultural College (US) 2026-04-08 — — EP disclosed
US-20260001861-A1 PYRIDINE CARBOXAMIDE COMPOUNDS FOR INHIBITING NAV1.8 LIEBER INST INC (US) 2026-01-01 — — US disclosed
US-12286436-B2 Substituted pyrimido[4,5-b]indoles as CK2 inhibitors King Faisal University (SA) 2025-04-29 — — US disclosed
US-12269826-B1 7H-pyrido[4′,3′:4,5]pyrrolo[2,3-c][1,7]naphthyridine compounds as CK2 inhibitors King Faisal University (SA) 2025-04-08 — — US disclosed
US-20250092048-A1 PYRIMIDO[4,5-B]INDOLE COMPOUNDS AS CK2 INHIBITORS UNIV KING FAISAL (SA) 2025-03-20 — — US disclosed
US-12240851-B1 Pyrido[3′,4′:4,5]pyrrolo[3,2-c]naphthyridine compounds as CK2 inhibitors King Faisal University (SA) 2025-03-04 — — US disclosed
US-20250066362-A1 PYRIDO[3',4':4,5]PYRROLO[3,2-C]NAPHTHYRIDINE COMPOUNDS AS CK2 INHIBITORS King Faisal University (SA) 2025-02-27 — — US disclosed
US-12234221-B2 Pyridine carboxamide compounds for inhibiting NAV1.8 LIEBER INSTITUTE, INC. (US) 2025-02-25 — — US disclosed
US-20030220350-A1 Glucagon antagonists/inverse agonists PFIZER INC 2003-11-27 — — US disclosed
US-6503949-B1 Treating Type 2 diabetes, hyperglycemia, impaired glucose tolerance or obesity NORO NORDISK A/S (DK) 2003-01-07 — — US disclosed
WO-1997037646-A1 CATECHOLAMINE SURROGATES USEFUL AS β3 AGONISTS BRISTOL-MYERS SQUIBB COMPANY (US) 1997-10-16 — — WO disclosed
EP-0372315-B1 Reactive dyes based on copper formazane BASF AG (DE) 1994-01-26 — — EP disclosed
US-5149789-A Triazine dyes BASF AKTIENGESELLSCHAFT (DE) 1992-09-22 — — US disclosed
US-5041540-A For dyeing or printing hydroxyl- or nitrogen-containing substrates BASF AKTIENGESELLSCHAFT (DE) 1991-08-20 — — US disclosed
EP-0391264-A1 Reactive dyes with two or three halogen-N-heterocycles as reactive groups BASF Aktiengesellschaft (DE) 1990-10-10 — — EP disclosed
EP-0372315-A1 Reactive dyes based on copper formazane BASF Aktiengesellschaft (DE) 1990-06-13 — — 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 (8 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-20250092048-A1 PYRIMIDO[4,5-B]INDOLE COMPOUNDS AS CK2 INHIBITORS SKP2, CDK2, CSNK2A1 LMNA 4391/4885CA2 969/4885CA12 3544/4885
US-20250066362-A1 PYRIDO[3',4':4,5]PYRROLO[3,2-C]NAPHTHYRIDINE COMPOUNDS AS CK2 INHIBITORS CKS2, CDK2, PNKP LMNA 2543/4885CA2 1164/4885CA12 4068/4885
US-12234221-B2 Pyridine carboxamide compounds for inhibiting NAV1.8 SCN8A, SCN1A, SCN2A LMNA 1580/4885CA2 613/4885CA12 3752/4885
US-12240851-B1 Pyrido[3′,4′:4,5]pyrrolo[3,2-c]naphthyridine compounds as CK2 inhibitors CKS2, CDK2, PNKP LMNA 2500/4885CA2 1181/4885CA12 4104/4885
US-20260001861-A1 PYRIDINE CARBOXAMIDE COMPOUNDS FOR INHIBITING NAV1.8 SCN8A, SCN1A, SCN1B LMNA 916/4885CA2 165/4885CA12 2568/4885
US-20030220350-A1 Glucagon antagonists/inverse agonists GLP1R, GPR119, GCGR LMNA 3643/4885CA2 3233/4885CA12 4759/4885
US-12269826-B1 7H-pyrido[4′,3′:4,5]pyrrolo[2,3-c][1,7]naphthyridine compounds as CK2 inhibitors CKS2, CSNK1G1, CSNK2A3 LMNA 2168/4885CA2 1380/4885CA12 4140/4885
US-12286436-B2 Substituted pyrimido[4,5-b]indoles as CK2 inhibitors SKP2, CDK2, CSNK2A1 LMNA 4535/4885CA2 974/4885CA12 3876/4885

“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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