SCHEMBL118090

SCHEMBL118090

COC(=O)c1cccc(C)n1

nearest known ligand 0.59

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
P2RX7 Q99572 1/20 0.59
CYP1A2 P05177 3/20 0.57
SMN1; SMN2 Q16637 2/20 0.57
RAB9A P51151 2/20 0.57
NPC1 O15118 1/20 0.57
TP53 P04637 1/20 0.57
CYP3A4 P08684 1/20 0.57
CYP2C9 P11712 1/20 0.57
CYP2C19 P33261 1/20 0.57
MEN1 O00255 1/20 0.56
KMT2A Q03164 1/20 0.56
GRM5 P41594 1/20 0.56
MAPT P10636 3/20 0.53
GAA P10253 1/20 0.53
RECQL P46063 1/20 0.53
ALDH1A1 P00352 1/20 0.49
KDM4E B2RXH2 1/20 0.48
MAPK1 P28482 1/20 0.47

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
SCHEMBL30212560 1.00 P2RX7 (0.59) P2RX7CYP1A2SMN1; SMN2RAB9ANPC1
Hydrochloric Acid SCHEMBL5728855 0.98 P2RX7 (0.58) P2RX7CYP1A2SMN1; SMN2RAB9ANPC1
SCHEMBL24581364 0.89 CCR1 (0.55) P2RX7CYP1A2SMN1; SMN2RAB9ANPC1
SCHEMBL69653 0.87 MAPT (0.64) CYP1A2SMN1; SMN2RAB9ANPC1TP53
SCHEMBL31325221 0.87 MAPT (0.49) P2RX7CYP1A2SMN1; SMN2RAB9ANPC1
SCHEMBL10759567 0.82 GRM5 (0.54) P2RX7CYP1A2SMN1; SMN2RAB9ANPC1
SCHEMBL20475333 0.82 MAPT (0.51) CYP1A2SMN1; SMN2RAB9ANPC1TP53
SCHEMBL13681299 0.82 P2RX7 (0.53) P2RX7CYP1A2SMN1; SMN2RAB9ANPC1
SCHEMBL16049654 0.82 P2RX7 (0.58) P2RX7CYP1A2SMN1; SMN2RAB9ANPC1
SCHEMBL23037197 0.82 MAPT (0.54) CYP1A2SMN1; SMN2RAB9ANPC1TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113649055-B Catalyst for selective hydrogenation of methyl picolinate and preparation method and application thereof 湖北大学 2023-03-24 CN claimed
CN-113649055-A Catalyst for selective hydrogenation of methyl picolinate and preparation method and application thereof 湖北大学 2021-11-16 CN claimed
EP-3112352-A1 OPIOID RECEPTOR MODULATORS Janssen Pharmaceutica NV (BE) 2017-01-04 EP claimed
EP-1725537-B1 NOVEL COMPOUNDS AS OPIOID RECEPTOR MODULATORS JANSSEN PHARMACEUTICA NV (BE) 2011-07-13 EP claimed
WO-2026098560-A2 BENZENE-CONTAINING POLYCYCLIC DERIVATIVE MODULATOR, PREPARATION METHOD THEREFOR AND USE THEREOF 上海翰森生物医药科技有限公司 2026-05-15 WO disclosed
US-20260049159-A1 ANTIBODY-ALK5 INHIBITOR CONJUGATES AND THEIR USES SYNTHIS THERAPEUTICS, INC. (US) 2026-02-19 US disclosed
US-12528815-B2 5-amino-8-(4-pyridyl)-[1,2,4]triazolo[4,3-c]pyrimidin-3-one compounds for use against cancer NXERA PHARMA UK LIMITED (GB) 2026-01-20 US disclosed
US-12473377-B2 Antibody-ALK5 inhibitor conjugates and their uses SYNTHIS THERAPEUTICS, INC. (US) 2025-11-18 US disclosed
US-20250339425-A1 Alpha9 and Alpha7 Nicotinic Acetylcholine Receptor Ligands UNIV NORTHEASTERN (US) 2025-11-06 US disclosed
EP-4232431-B1 COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH LPA RECEPTOR ACTIVITY LHOTSE BIO INC (US) 2025-08-13 EP disclosed
US-20250215017-A1 TGF-ß INHIBITOR COMPOUND AND USE THEROF MEDINNO PHARMACEUTICAL TECHNOLOGY (ZHUHAI) CO., LTD. (CN) 2025-07-03 US disclosed
US-20250179094-A1 TGF-B INHIBITOR COMPOUND AND USE THEREOF MEDINNO PHARMACEUTICAL TECHNOLOGY (ZHUHAI) CO., LTD. (CN) 2025-06-05 US disclosed
US-6476021-B1 Compounds having cGMP-PDE inhibitory effect MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 2002-11-05 US disclosed
WO-2002066462-A1 PYRAZOLE DERIVATIVES AGAINST TGF OVEREXPRESSION GLAXO GROUP LIMITED (GB) 2002-08-29 WO disclosed
WO-2002062776-A1 2-AMINO-4-(PYRIDIN-2-YL)-THIAZOLE DERIVATIVES AS TRANSFORMING GROWTH FACTOR BETA (TGF-BETA) INHIBITORS GLAXO GROUP LIMITED (GB) 2002-08-15 WO disclosed
WO-2002062787-A1 PYRAZOLES AS TGF INHIBITORS GLAXO GROUP LIMITED (GB) 2002-08-15 WO disclosed
WO-2002062794-A2 COMPOUNDS GLAXO GROUP LIMITED (GB) 2002-08-15 WO disclosed
EP-1048666-A1 NOVEL COMPOUNDS HAVING cGMP-PDE INHIBITORY EFFECT MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 2000-11-02 EP disclosed
US-5114945-A Spiropiperidine derivatives GLAXO GROUP LIMITED (GB) 1992-05-19 US disclosed
EP-0330461-A2 Piperidine derivatives GLAXO GROUP LIMITED (GB) 1989-08-30 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 (6 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-20250339425-A1 Alpha9 and Alpha7 Nicotinic Acetylcholine Receptor Ligands CHRNA9, CHRNA7, CHRNA1 P2RX7 19/4885CYP1A2 1668/4885SMN1; SMN2 2910/4885
US-20250179094-A1 TGF-B INHIBITOR COMPOUND AND USE THEREOF TGFB1, TGFB2, TGFBR1 P2RX7 3502/4885CYP1A2 2051/4885SMN1; SMN2 3437/4885
US-12473377-B2 Antibody-ALK5 inhibitor conjugates and their uses ALK, ALKBH5, ALKBH3 P2RX7 4265/4885CYP1A2 2565/4885SMN1; SMN2 3523/4885
US-20260049159-A1 ANTIBODY-ALK5 INHIBITOR CONJUGATES AND THEIR USES ALK, CD2, TGFBR2 P2RX7 3684/4885CYP1A2 3047/4885SMN1; SMN2 3447/4885
US-12528815-B2 5-amino-8-(4-pyridyl)-[1,2,4]triazolo[4,3-c]pyrimidin-3-one compounds for use against cancer ADORA1, ADORA3, OPRL1 P2RX7 55/4885CYP1A2 1308/4885SMN1; SMN2 1824/4885
US-20250215017-A1 TGF-ß INHIBITOR COMPOUND AND USE THEROF TGFB1, TGFB2, TGFBR2 P2RX7 3750/4885CYP1A2 3248/4885SMN1; SMN2 3159/4885

“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.