SCHEMBL325226

SCHEMBL325226

COC(OC)c1ccc2cccnc2n1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.46
KDM4E B2RXH2 2/20 0.46
KMT2A Q03164 2/20 0.46
MEN1 O00255 1/20 0.46
ALDH1A1 P00352 2/20 0.43
OGA O60502 1/20 0.40
SMN1; SMN2 Q16637 2/20 0.38
MAPT P10636 2/20 0.38
CCR1 P32246 2/20 0.38
CCR5 P51681 2/20 0.38
CCR8 P51685 2/20 0.38
ALOX15 P16050 2/20 0.38
HTT P42858 2/20 0.38
GMNN O75496 1/20 0.38
TP53 P04637 1/20 0.38
HSP90AA1 P07900 1/20 0.38
MMP2 P08253 1/20 0.38
CYP3A4 P08684 1/20 0.38
CYP2D6 P10635 1/20 0.38
MMP9 P14780 1/20 0.38

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
SCHEMBL25574445 0.84 ALDH1A1 (0.42) LMNAKDM4EKMT2AMEN1ALDH1A1
SCHEMBL2611076 0.79 ALDH1A1 (0.47) LMNAKDM4EKMT2AMEN1ALDH1A1
SCHEMBL19283903 0.76 LMNA (0.47) LMNAKDM4EKMT2AMEN1ALDH1A1
SCHEMBL19283998 0.76 ALDH1A1 (0.44) LMNAKDM4EKMT2AMEN1ALDH1A1
SCHEMBL16668566 0.74 L3MBTL1 (0.38) ALDH1A1SMN1; SMN2MAPTCCR1CCR5
SCHEMBL12045706 0.74 ALDH1A1 (0.42) LMNAKDM4EKMT2AMEN1ALDH1A1
SCHEMBL22807296 0.73 CCR1 (0.42) KDM4EKMT2AALDH1A1SMN1; SMN2CCR1
SCHEMBL1424278 0.73 ALDH1A1 (0.48) LMNAKDM4EKMT2AMEN1ALDH1A1
SCHEMBL30441269 0.73 ALDH1A1 (0.48) LMNAKDM4EKMT2AMEN1ALDH1A1
SCHEMBL4741484 0.72 CYP1A2 (0.47) LMNAKDM4EKMT2AALDH1A1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116003400-B 2-Formyl tetrahydronaphthyridine compound and medicinal composition and application thereof 暨南大学 2025-05-02 CN disclosed
WO-2024083086-A1 BICYCLIC DERIVATIVE INTEGRIN INHIBITOR 上海如凌生物医药有限公司 2024-04-25 WO disclosed
CN-117903171-A Integrin inhibitors of a class of bicyclic derivatives 上海如凌生物医药有限公司 2024-04-19 CN disclosed
CN-114100588-B Nitrogen-containing functional group ultrahigh crosslinked adsorbent, preparation method thereof and blood perfusion device 泉州师范学院 2024-03-22 CN disclosed
US-11667631-B2 FGFR4 inhibitor, preparation method therefor, and applications thereof JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2023-06-06 US disclosed
US-11667631-B2 FGFR4 inhibitor, preparation method therefor, and applications thereof JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2023-06-06 US disclosed
CN-116003400-A 2-formyl tetrahydronaphthyridine compound and medicinal composition and application thereof 暨南大学 2023-04-25 CN disclosed
US-11608332-B2 FGFR4 inhibitor and preparation method and use thereof JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2023-03-21 US disclosed
US-20220362245-A1 COMPOUNDS FOR INHIBITING FGFR4 TERNS PHARMACEUTICALS, INC. (US) 2022-11-17 US disclosed
CN-113234072-B FGFR4 inhibitor, preparation method and application thereof 江苏豪森药业集团有限公司 2022-11-04 CN disclosed
US-20030229079-A1 1-(Aromatic- or heteroaromatic-substituted)-3-(heteroaromatic substituted)-1,3-propanediones and uses thereof PAYNE LINDA S (US) 2003-12-11 US disclosed
US-6514964-B1 Treating diseases, conditions or disorders mediated by integrin receptors, such as vitronectin and fibronectin receptors AMGEN INC. 2003-02-04 US disclosed
EP-1196384-A4 1-(AROMATIC- OR HETEROAROMATIC-SUBSTITUTED)-3-(HETEROAROMATIC SUBSTITUTED)-1,3-PROPANEDIONES AND USES THEREOF MERCK & CO INC (US) 2002-10-23 EP disclosed
EP-1196384-A1 1-(AROMATIC- OR HETEROAROMATIC-SUBSTITUTED)-3-(HETEROAROMATIC SUBSTITUTED)-1,3-PROPANEDIONES AND USES THEREOF Merck & Co., Inc. (US) 2002-04-17 EP disclosed
US-20020010176-A1 Integrin receptor antagonists MERCK SHARP & DOHME CORP. 2002-01-24 US disclosed
US-6297249-B1 SUBSTITUTED 2-CARBOXYALKYLPYRIDINES MERCK & CO., INC. 2001-10-02 US disclosed
US-6211184-B1 TETRAHYDRO-PYRAZINE OR PYRIMIDINE DERIVATIVES; VITRONECTIN RECEPTOR ANTAGONIST; OSTEOPOROSIS; ANTIINFLAMMATORY, ANTITUMOR AGENTS; ANGIOGENESIS AND RESTENOSIS INHIBITORS MERCK & CO., INC. 2001-04-03 US disclosed
WO-2001000578-A1 1-(AROMATIC- OR HETEROAROMATIC-SUBSTITUTED)-3-(HETEROAROMATIC SUBSTITUTED)-1,3-PROPANEDIONES AND USES THEREOF MERCK & CO., INC. (US) 2001-01-04 WO disclosed
US-6048861-A OSTEOPOROSIS; BONE DISORDERS; CARDIOVASCULAR DISORDERS; ANTIINFLAMMATROY AGENTS; WOUND HEALING AGENTS MERCK & CO., INC. (US) 2000-04-11 US disclosed
US-5981546-A Integrin antagonists MERCK & CO., INC. (US) 1999-11-09 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-11667631-B2 FGFR4 inhibitor, preparation method therefor, and applications thereof FGFR4, FGFR1, FGFR2 LMNA 4571/4885KDM4E 1217/4885KMT2A 2300/4885
US-20030229079-A1 1-(Aromatic- or heteroaromatic-substituted)-3-(heteroaromatic substituted)-1,3-propanediones and uses thereof CYP2S1, IMPDH1, IDO1 LMNA 3637/4885KDM4E 1768/4885KMT2A 3589/4885
US-11608332-B2 FGFR4 inhibitor and preparation method and use thereof FGFR4, FGFR1, FGFR2 LMNA 4675/4885KDM4E 583/4885KMT2A 1907/4885
US-20020010176-A1 Integrin receptor antagonists ITGAV, ITGB3, ADGRE5 LMNA 3788/4885KDM4E 2532/4885KMT2A 4230/4885
US-20220362245-A1 COMPOUNDS FOR INHIBITING FGFR4 FGFR4, FGFR1, FGFR3 LMNA 3880/4885KDM4E 250/4885KMT2A 1241/4885

“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.