SCHEMBL3110403

SCHEMBL3110403

CSc1nc(O)cc(Cl)n1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 6/20 0.51
MEN1 O00255 4/20 0.51
GAA P10253 1/20 0.51
SMN1; SMN2 Q16637 1/20 0.51
POLB P06746 1/20 0.50
HTT P42858 1/20 0.46
MAPK1 P28482 1/20 0.36
KDM4E B2RXH2 3/20 0.33
LMNA P02545 1/20 0.33
CYP1A2 P05177 1/20 0.33
CYP3A4 P08684 1/20 0.33
CYP2C9 P11712 1/20 0.33
CYP2C19 P33261 1/20 0.33
NPSR1 Q6W5P4 1/20 0.33
RXFP1 Q9HBX9 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
THRB P10828 1/20 0.33
HSP90AA1 P07900 2/20 0.32
PKM P14618 1/20 0.32

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
SCHEMBL62021 0.84 POLB (0.53) KMT2AMEN1GAASMN1; SMN2POLB
SCHEMBL537673 0.84 MAPK1 (0.42) KMT2AMEN1GAASMN1; SMN2POLB
SCHEMBL28715240 0.81 MAPK1 (0.41) KMT2AMEN1GAASMN1; SMN2POLB
SCHEMBL29352953 0.81 MAPK1 (0.41) KMT2AMEN1GAASMN1; SMN2POLB
SCHEMBL10389212 0.81 MAPK1 (0.41) KMT2AMEN1GAASMN1; SMN2POLB
SCHEMBL10389241 0.81 MAPK1 (0.41) KMT2AMEN1GAASMN1; SMN2POLB
SCHEMBL1271823 0.78 POLB (0.39) KMT2AMEN1GAASMN1; SMN2POLB
SCHEMBL1598214 0.76 KMT2A (0.49) KMT2AMEN1GAAPOLBHTT
SCHEMBL1902046 0.76 POLB (0.47) KMT2AMEN1GAASMN1; SMN2POLB
SCHEMBL19805989 0.74 POLB (0.46) KMT2AMEN1GAASMN1; SMN2POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250092042-A1 HETEROARYL SUBSTITUTED SPIROPIPERIDINYL DERIVATIVES AND PHARMACEUTICAL USES THEREOF NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH, INC. 2025-03-20 US disclosed
US-12157737-B2 Heteroaryl substituted spiropiperidinyl derivatives and pharmaceutical uses thereof NOVARTIS AG (CH) 2024-12-03 US disclosed
US-20240043425-A1 HETEROARYL SUBSTITUTED SPIROPIPERIDINYL DERIVATIVES AND PHARMACEUTICAL USES THEREOF NOVARTIS AG (CH) 2024-02-08 US disclosed
US-11708366-B2 Heteroaryl substituted spiropiperidinyl derivatives and pharmaceutical uses thereof NOVARTIS AG (CH) 2023-07-25 US disclosed
US-11708366-B2 Heteroaryl substituted spiropiperidinyl derivatives and pharmaceutical uses thereof NOVARTIS AG (CH) 2023-07-25 US disclosed
US-11708366-B2 Heteroaryl substituted spiropiperidinyl derivatives and pharmaceutical uses thereof NOVARTIS AG (CH) 2023-07-25 US disclosed
US-11685740-B2 Bicyclic nitrogen-containing heterocyclic derivatives and pharmaceutical composition comprising the same SHIONOGI & CO., LTD. (JP) 2023-06-27 US disclosed
US-11685740-B2 Bicyclic nitrogen-containing heterocyclic derivatives and pharmaceutical composition comprising the same SHIONOGI & CO., LTD. (JP) 2023-06-27 US disclosed
EP-4196478-A1 HETEROARYL SUBSTITUTED SPIROPIPERIDINYL DERIVATIVES AND PHARMACEUTICAL USES THEREOF Novartis AG (CH) 2023-06-21 EP disclosed
CN-116157404-A Heteroaryl substituted spiropiperidinyl derivatives and pharmaceutical uses thereof 诺华股份有限公司 2023-05-23 CN disclosed
US-6562970-B1 Method for producing 4-chloro-6-hydroxypyrimidine BAYER AKTIENGESELLSCHAFT (DE) 2003-05-13 US disclosed
EP-1194413-A1 METHOD FOR PRODUCING 4-CHLORO-6-HYDROXYPYRIMIDINE Bayer Aktiengesellschaft (DE) 2002-04-10 EP disclosed
WO-2001000593-A1 METHOD FOR PRODUCING 4-CHLORO-6-HYDROXYPYRIMIDINE BAYER AKTIENGESELLSCHAFT (DE) 2001-01-04 WO disclosed
WO-2000046212-A1 METHOD OF PRODUCING SUBSTITUTED PYRIMIDINE DERIVATIVES SYNGENTA PARTICIPATIONS AG (CH) 2000-08-10 WO disclosed
EP-0468069-B1 Process for producing a 4,6-bis(difluoromethoxy)-2-alkylthiopyrimidine ASAHI GLASS CO LTD (JP) 1996-10-02 EP disclosed
EP-0244359-B1 PROCESS FOR THE PREPARATION OF PYRIMIDINE DERIVATIVES CIBA-GEIGY AG (CH) 1992-07-22 EP disclosed
EP-0468069-A1 Process for producing a 4,6-bis(difluoromethoxy)-2-alkylthiopyrimidine ASAHI GLASS COMPANY LTD. (JP) 1992-01-29 EP disclosed
US-5071982-A Process for producing a 4,6-bis(difluoromethoxy)-2-alkylthiopyrimidine ASAHI GLASS CO., LTD. (JP) 1991-12-10 US disclosed
EP-0244359-A2 Process for the preparation of pyrimidine derivatives CIBA-GEIGY AG (CH) 1987-11-04 EP disclosed
US-4692524-A HERBICIDE INTERMEDIATES CIBA-GEIGY CORPORATION (US) 1987-09-08 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 (5 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-12157737-B2 Heteroaryl substituted spiropiperidinyl derivatives and pharmaceutical uses thereof REN, NR3C2, PKD1 KMT2A 3399/4885MEN1 1544/4885GAA 2599/4885
US-11708366-B2 Heteroaryl substituted spiropiperidinyl derivatives and pharmaceutical uses thereof REN, NR3C2, PKD1 KMT2A 3399/4885MEN1 1544/4885GAA 2599/4885
US-20240043425-A1 HETEROARYL SUBSTITUTED SPIROPIPERIDINYL DERIVATIVES AND PHARMACEUTICAL USES THEREOF REN, NR3C2, PKD1 KMT2A 3399/4885MEN1 1544/4885GAA 2599/4885
US-20250092042-A1 HETEROARYL SUBSTITUTED SPIROPIPERIDINYL DERIVATIVES AND PHARMACEUTICAL USES THEREOF REN, PKD1, PKD2 KMT2A 2996/4885MEN1 1485/4885GAA 2233/4885
US-11685740-B2 Bicyclic nitrogen-containing heterocyclic derivatives and pharmaceutical composition comprising the same P2RX7, P2RX2, P2RX1 KMT2A 2254/4885MEN1 2921/4885GAA 4667/4885

“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.