SCHEMBL687474

SCHEMBL687474

CNS(=O)(=O)c1cccc(N)c1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.61
POLB P06746 2/20 0.61
CA2 P00918 2/20 0.59
CA12 O43570 1/20 0.59
CA1 P00915 1/20 0.59
CA4 P22748 1/20 0.59
CA9 Q16790 1/20 0.59
CA14 Q9ULX7 1/20 0.59
F2 P00734 3/20 0.57
PRSS1 P07477 3/20 0.57
PRSS2 P07478 3/20 0.57
PRSS3 P35030 3/20 0.57
CYP19A1 P11511 1/20 0.57
ALDH1A1 P00352 2/20 0.57
TSHR P16473 1/20 0.57
HSD17B10 Q99714 1/20 0.57
TDP1 Q9NUW8 1/20 0.57
PKM P14618 2/20 0.56
PRMT1 Q99873 1/20 0.53
L3MBTL1 Q9Y468 1/20 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
Hydrochloric Acid SCHEMBL14832025 0.98 POLB (0.59) LMNAPOLBCA2CA12CA1
SCHEMBL2242660 0.85 L3MBTL1 (0.61) LMNACA2CA12CA1CA4
SCHEMBL22916894 0.82 LMNA (0.63) LMNAPOLBCA2CA12CA1
SCHEMBL11406378 0.82 LMNA (0.63) LMNAPOLBCA2CA12CA1
SCHEMBL5566217 0.81 POLB (0.57) LMNAPOLBCA2CA12CA1
SCHEMBL1684425 0.80 CA2 (0.65) LMNACA2CA12CA1CA4
SCHEMBL31475667 0.80 CA2 (0.68) LMNACA2CA12CA1CA4
SCHEMBL7142664 0.80 CA2 (0.68) LMNACA2CA12CA1CA4
SCHEMBL922755 0.79 CYP19A1 (0.66) LMNAPOLBCA2CA12CA1
SCHEMBL2018411 0.79 LMNA (0.69) LMNAPOLBCA2CA12CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110857301-B Method for preparing TNNI3K inhibitor 南京理工大学 2022-07-22 CN claimed
CN-109422748-B Method for synthesizing TNNI3K inhibitor 南京理工大学 2021-06-22 CN claimed
CN-110857301-A Method for preparing TNNI3K inhibitor 南京理工大学 2020-03-03 CN claimed
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
US-20260078114-A1 COMPOUND USED AS INHIBITOR OF CDK4 KINASE AND USE THEREOF TYK MEDICINES INC (CN) 2026-03-19 US disclosed
EP-4585595-A1 COMPOUND USED AS INHIBITOR OF CDK4 KINASE AND USE THEREOF TYK Medicines, Inc. (CN) 2025-07-16 EP disclosed
US-12319676-B2 Substituted amide compounds useful as farnesoid X receptor modulators BRISTOL-MYERS SQUIBB COMPANY (US) 2025-06-03 US disclosed
US-12269827-B1 Substituted pyrazino[1′,2′:1,5]pyrazolo[4,3-c][1,6]naphthyridines as CK2 inhibitors King Faisal University (SA) 2025-04-08 US disclosed
US-12258345-B1 Pyrrolo[3,2-c]isoquinoline-2,3-dione compounds as CK2 inhibitors King Faisal University (SA) 2025-03-25 US disclosed
WO-2025051211-A1 COMPOUND USED AS CDK4 KINASE INHIBITOR AND USE THEREOF 浙江同源康医药股份有限公司 2025-03-13 WO disclosed
WO-2003045379-A1 HYDRAZONOPYRAZOLE DERIVATIVES AND THEIR USE AS THERAPEUTICS KINETEK PHARMACEUTICALS, INC. (CA) 2003-06-05 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
US-4153413-A DYEING POLYESTER OR CELLULOSE TRIACETATE WITH A DISPERSE AZO DYESTUFF, HEAT TREATMENT, PADDING, PRINTING IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1979-05-08 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 (4 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-12319676-B2 Substituted amide compounds useful as farnesoid X receptor modulators NR1H4, FXR1, NR1H3 LMNA 2299/4885POLB 3415/4885CA2 1816/4885
US-20260078114-A1 COMPOUND USED AS INHIBITOR OF CDK4 KINASE AND USE THEREOF CDK4, CDK1, CDK3 LMNA 505/4885POLB 607/4885CA2 2851/4885
US-12269827-B1 Substituted pyrazino[1′,2′:1,5]pyrazolo[4,3-c][1,6]naphthyridines as CK2 inhibitors CSNK1A1, CSNK1G1, CSNK2A1 LMNA 2624/4885POLB 712/4885CA2 1013/4885
US-12258345-B1 Pyrrolo[3,2-c]isoquinoline-2,3-dione compounds as CK2 inhibitors CSNK2A3, CSNK2A1, CSNK2A2 LMNA 3520/4885POLB 416/4885CA2 725/4885

“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.