SCHEMBL22040325

SCHEMBL22040325

CC1(C)OB(c2cccnc2OC2CC2)OC1(C)C

nearest known ligand 0.41

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
▸ ROCK2 O75116 1/20 0.41
▸ PDE10A Q9Y233 8/20 0.37
▸ LIPE Q05469 2/20 0.34
▸ LRRK2 Q5S007 1/20 0.33
▸ ALOX5AP P20292 1/20 0.32
▸ FEN1 P39748 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
SCHEMBL29513574 1.00 ROCK2 (0.41) ROCK2PDE10ALIPELRRK2ALOX5AP
SCHEMBL31441507 0.94 ROCK2 (0.40) ROCK2PDE10ALIPELRRK2ALOX5AP
SCHEMBL31441748 0.94 ROCK2 (0.40) ROCK2PDE10ALRRK2ALOX5APFEN1
SCHEMBL25429896 0.93 ROCK2 (0.40) ROCK2PDE10ALRRK2ALOX5APFEN1
SCHEMBL31441478 0.92 LRRK2 (0.43) ROCK2PDE10ALRRK2ALOX5APFEN1
SCHEMBL31441548 0.87 LRRK2 (0.45) ROCK2PDE10ALRRK2
SCHEMBL31441643 0.81 ROCK2 (0.42) ROCK2
SCHEMBL365301 0.81 L3MBTL1 (0.36) LIPE
SCHEMBL29900384 0.81 L3MBTL1 (0.36) LIPE
SCHEMBL12098073 0.81 ALOX5AP (0.35) ROCK2LIPEALOX5APFEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240043420-A1 7-AZAINDOLE COMPOUNDS FOR INHIBITION OF BCR-ABL TYROSINE KINASES ENLIVEN INC. 2024-02-08 — — US disclosed
US-11851425-B2 Combination treatments comprising administration of 1H-pyrazolo[4,3-B]pyridines H. LUNDBECK A/S (DK) 2023-12-26 — — US disclosed
US-11834449-B2 TYK2 inhibitors and uses thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2023-12-05 — — US disclosed
US-11834449-B2 TYK2 inhibitors and uses thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2023-12-05 — — US disclosed
EP-4225741-A1 7-AZAINDOLE COMPOUNDS FOR INHIBITION OF BCR-ABL TYROSINE KINASES Enliven Therapeutics, Inc. (US) 2023-08-16 — — EP disclosed
CN-116438182-A 7-azaindole compounds for inhibiting BCR-ABL tyrosine kinase 活力疗法公司 2023-07-14 — — CN disclosed
CN-111556871-B 1H-pyrazolo [4,3-b ] pyridines as PDE1 inhibitors H.隆德贝克有限公司 2023-07-07 — — CN disclosed
US-11634416-B2 Combination treatments comprising administration of 1H-pyrazolo[4,3-b]pyridines H. LUNDBECK A/S (DK) 2023-04-25 — — US disclosed
US-11491140-B2 1H-pyrazolo[4,3-b]pyridines as PDE1 inhibitors H. LUNDBECK A/S (DK) 2022-11-08 — — US disclosed
CN-111465410-B Combination therapy comprising administration of 1H-pyrazolo [4,3-B ] pyridine H.隆德贝克有限公司 2022-10-25 — — CN disclosed
EP-3689874-A1 1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS H. Lundbeck A/S (DK) 2020-08-05 — — EP disclosed
CN-111465410-A Combination therapy comprising administration of 1H-pyrazolo [4,3-B ] pyridine H.隆德贝克有限公司 2020-07-28 — — CN disclosed
US-20200172540-A1 TYK2 INHIBITORS AND USES THEREOF TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2020-06-04 — — US disclosed
WO-2020112937-A1 TYK2 INHIBITORS AND USES THEREOF NIMBUS LAKSHMI, INC. (US) 2020-06-04 — — WO disclosed
US-20200129480-A1 1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS H. LUNDBECK A/S (DK) 2020-04-30 — — US disclosed
EP-3478681-B1 1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS H LUNDBECK AS (DK) 2020-02-26 — — EP disclosed
US-20190194189-A1 1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS H. LUNDBECK A/S (DK) 2019-06-27 — — US disclosed
US-20190105302-A1 1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS H. LUNDBECK A/S (DK) 2019-04-11 — — US disclosed
US-10034861-B2 1H-pyrazolo[4,3-b]pyridines as PDE1 inhibitors H. LUNDBECK A/S (DK) 2018-07-31 — — US disclosed
US-20180000786-A1 1H-Pyrazolo[4,3-b]pyridines as PDE1 Inhibitors H. LUNDBECK A/S (DK) 2018-01-04 — — 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 (11 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-11834449-B2 TYK2 inhibitors and uses thereof TYK2, JAK2, JAK1 ROCK2 246/4885PDE10A 4705/4885LIPE 4670/4885
US-20200129480-A1 1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS PDE3A, PDE5A, PDE12 ROCK2 707/4885PDE10A 15/4885LIPE 3637/4885
US-10034861-B2 1H-pyrazolo[4,3-b]pyridines as PDE1 inhibitors PDE3A, PDE5A, PDE12 ROCK2 707/4885PDE10A 15/4885LIPE 3637/4885
US-11851425-B2 Combination treatments comprising administration of 1H-pyrazolo[4,3-B]pyridines PDE3B, PDE1B, PDE12 ROCK2 1003/4885PDE10A 18/4885LIPE 4139/4885
US-11491140-B2 1H-pyrazolo[4,3-b]pyridines as PDE1 inhibitors PDE3A, PDE5A, PDE12 ROCK2 678/4885PDE10A 15/4885LIPE 3654/4885
US-11634416-B2 Combination treatments comprising administration of 1H-pyrazolo[4,3-b]pyridines PDE1B, PDE3B, PDE1A ROCK2 1055/4885PDE10A 19/4885LIPE 3947/4885
US-20240043420-A1 7-AZAINDOLE COMPOUNDS FOR INHIBITION OF BCR-ABL TYROSINE KINASES ABL1, ABL2, BCR ROCK2 196/4885PDE10A 1988/4885LIPE 4707/4885
US-20180000786-A1 1H-Pyrazolo[4,3-b]pyridines as PDE1 Inhibitors PDE3A, PDE5A, PDE12 ROCK2 707/4885PDE10A 15/4885LIPE 3637/4885
US-20190194189-A1 1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS PDE12, PDE3B, PDE5A ROCK2 748/4885PDE10A 15/4885LIPE 3425/4885
US-20200172540-A1 TYK2 INHIBITORS AND USES THEREOF TYK2, JAK2, JAK1 ROCK2 246/4885PDE10A 4705/4885LIPE 4670/4885
US-20190105302-A1 1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS PDE3A, PDE5A, PDE12 ROCK2 707/4885PDE10A 15/4885LIPE 3637/4885

“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.

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