SCHEMBL17437883

SCHEMBL17437883

O=C(O)c1cnn2ccc(N3CCOCC3)cc12

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EPHB3 P54753 2/20 0.63
KMO O15229 1/20 0.48
SLC16A3 O15427 1/20 0.46
PKM P14618 2/20 0.45
ALDH1A1 P00352 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
PRKDC P78527 2/20 0.43
PIK3CA P42336 2/20 0.42
PIK3CD O00329 1/20 0.42
PIK3CB P42338 1/20 0.42
PIK3CG P48736 1/20 0.42
BRD9 Q9H8M2 2/20 0.42
BAZ2B Q9UIF8 2/20 0.42
L3MBTL1 Q9Y468 2/20 0.41
PIK3C2B O00750 1/20 0.41
KDM4E B2RXH2 2/20 0.41
MEN1 O00255 2/20 0.41
KMT2A Q03164 2/20 0.41
POLB P06746 2/20 0.41
TDP1 Q9NUW8 1/20 0.41

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
SCHEMBL17454455 0.88 EPHB3 (0.62) EPHB3KMOALDH1A1PRKDCBRD9
SCHEMBL27431439 0.88 EPHB3 (0.62) EPHB3KMOPRKDCBRD9BAZ2B
SCHEMBL15039556 0.88 EPHB3 (0.60) EPHB3ALDH1A1L3MBTL1KDM4EMEN1
SCHEMBL17452618 0.85 EPHB3 (0.59) EPHB3KMOALDH1A1PRKDCBRD9
SCHEMBL31469893 0.82 EPHB3 (0.56) EPHB3PKMALDH1A1SMN1; SMN2PIK3CA
SCHEMBL24567287 0.81 EPHB3 (0.53) EPHB3KMOPKMALDH1A1SMN1; SMN2
SCHEMBL17437981 0.80 ROCK2 (0.47) EPHB3KMOSLC16A3PKMALDH1A1
SCHEMBL2875489 0.78 EPHB3 (1.00) EPHB3KDM4EKMT2A
SCHEMBL20220366 0.78 EPHB3 (0.59) EPHB3PKMALDH1A1SMN1; SMN2PIK3CA
SCHEMBL33913 0.78 SMPD3 (0.55) EPHB3ALDH1A1SMN1; SMN2PRKDCPIK3CA

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260049080-A1 WILD TYPE KIT INHIBITORS BLUEPRINT MEDICINES CORP (US) 2026-02-19 US disclosed
US-12448379-B2 Wild type kit inhibitors BLUEPRINT MEDICINES CORPORATION (US) 2025-10-21 US disclosed
US-20250051363-A1 Substituted Pyrazolopyridines NEURO3 THERAPEUTICS INC (US) 2025-02-13 US disclosed
WO-2025029897-A1 SUBSTITUTED PYRAZOLOPYRIDINES NEURO3 THERAPEUTICS, INC. (US) 2025-02-06 WO disclosed
US-20240262826-A1 WILD TYPE KIT INHIBITORS BLUEPRINT MEDICINES CORPORATION 2024-08-08 US disclosed
WO-2024118887-A1 N-PHENYL-PYRAZOLO[1,5-A]PYRIDINE-3-CARBOXAMIDE DERIVATIVES AS WILD TYPE C-KIT KINASE INHIBITORS FOR THE TREATMENT OF URTICARIA BLUEPRINT MEDICINES CORPORATION (US) 2024-06-06 WO disclosed
CN-106817899-B Spiroheptane as ROCK inhibitor 百时美施贵宝公司 2021-03-09 CN disclosed
EP-3169682-B1 SPIROCYCLOHEPTANES AS INHIBITORS OF ROCK BRISTOL MYERS SQUIBB CO (US) 2018-12-26 EP disclosed
US-20180155296-A1 SPIROCYCLOHEPTANES AS INHIBITORS OF ROCK BRISTOL MYERS SQUIBB CO (US) 2018-06-07 US disclosed
US-20180155296-A1 SPIROCYCLOHEPTANES AS INHIBITORS OF ROCK BRISTOL MYERS SQUIBB CO (US) 2018-06-07 US disclosed
US-20180155296-A1 SPIROCYCLOHEPTANES AS INHIBITORS OF ROCK BRISTOL MYERS SQUIBB CO (US) 2018-06-07 US disclosed
US-9902702-B2 Spirocycloheptanes as inhibitors of rock BRISTOL-MYERS SQUIBB COMPANY (US) 2018-02-27 US disclosed
US-9902702-B2 Spirocycloheptanes as inhibitors of rock BRISTOL-MYERS SQUIBB COMPANY (US) 2018-02-27 US disclosed
US-9902702-B2 Spirocycloheptanes as inhibitors of rock BRISTOL-MYERS SQUIBB COMPANY (US) 2018-02-27 US disclosed
US-20160016914-A1 SPIROCYCLOHEPTANES AS INHIBITORS OF ROCK BRISTOL-MYERS SQUIBB COMPANY 2016-01-21 US disclosed
US-20160016914-A1 SPIROCYCLOHEPTANES AS INHIBITORS OF ROCK BRISTOL-MYERS SQUIBB COMPANY 2016-01-21 US disclosed
US-20160016914-A1 SPIROCYCLOHEPTANES AS INHIBITORS OF ROCK BRISTOL-MYERS SQUIBB COMPANY 2016-01-21 US disclosed
WO-2016010950-A1 SPIROCYCLOHEPTANES AS INHIBITORS OF ROCK BRISTOL-MYERS SQUIBB COMPANY (US) 2016-01-21 WO 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-20250051363-A1 Substituted Pyrazolopyridines QDPR, DPYD, P2RX4 EPHB3 2310/4885KMO 3512/4885SLC16A3 3305/4885
US-20260049080-A1 WILD TYPE KIT INHIBITORS KIT, CSNK1A1, CSNK1A1L EPHB3 2198/4885KMO 1447/4885SLC16A3 1252/4885
US-12448379-B2 Wild type kit inhibitors KIT, TNK1, TNNI3K EPHB3 2426/4885KMO 3143/4885SLC16A3 1484/4885
US-20240262826-A1 WILD TYPE KIT INHIBITORS KIT, TNK1, TNNI3K EPHB3 2426/4885KMO 3143/4885SLC16A3 1484/4885
US-20180155296-A1 SPIROCYCLOHEPTANES AS INHIBITORS OF ROCK ROCK1, MYLK, ROCK2 EPHB3 1833/4885KMO 953/4885SLC16A3 3798/4885
US-20160016914-A1 SPIROCYCLOHEPTANES AS INHIBITORS OF ROCK ROCK1, MYLK, ROCK2 EPHB3 1833/4885KMO 953/4885SLC16A3 3798/4885

“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.