SCHEMBL250345

SCHEMBL250345

O=C1Nc2cc(Cl)ccc2C1=Cc1cccc(Cl)c1F

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MDM2 Q00987 2/20 0.53
▸ TUBB4A P04350 2/20 0.49
▸ TUBB P07437 2/20 0.49
▸ TUBA3C P0DPH7 2/20 0.49
▸ TUBA1B P68363 2/20 0.49
▸ TUBA4A P68366 2/20 0.49
▸ TUBB4B P68371 2/20 0.49
▸ TUBB3 Q13509 2/20 0.49
▸ TUBB2A Q13885 2/20 0.49
▸ TUBB8 Q3ZCM7 2/20 0.49
▸ TUBA3E Q6PEY2 2/20 0.49
▸ TUBA1A Q71U36 2/20 0.49
▸ TUBA1C Q9BQE3 2/20 0.49
▸ TUBB6 Q9BUF5 2/20 0.49
▸ TUBB2B Q9BVA1 2/20 0.49
▸ TUBB1 Q9H4B7 2/20 0.49
▸ NPC1 O15118 1/20 0.49
▸ LRRK2 Q5S007 2/20 0.47
▸ CES1 P23141 1/20 0.47
▸ PDGFRB P09619 3/20 0.44

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
SCHEMBL29776573 1.00 MDM2 (0.53) MDM2TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL29443894 1.00 MDM2 (0.53) MDM2TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL223844 1.00 MDM2 (0.53) MDM2TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL29875754 0.90 LRRK2 (0.60) MDM2LRRK2PDGFRBCDK2TGM2
SCHEMBL28711339 0.90 LRRK2 (0.60) MDM2LRRK2PDGFRBCDK2TGM2
SCHEMBL14659628 0.90 NPC1 (0.56) MDM2TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL14659629 0.90 NPC1 (0.56) MDM2TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL2739255 0.88 NPC1 (0.47) MDM2NPC1PDGFRBTGM2MEN1
SCHEMBL14658998 0.88 MEN1 (0.52) MDM2NPC1PDGFRBMEN1KMT2A
SCHEMBL6822268 0.88 NPC1 (0.47) MDM2NPC1PDGFRBMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8742121-B2 Process for the preparation of small molecule inhibitors of MDM2 and intermediates used therein THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2014-06-03 — — US claimed
US-20130030173-A1 PROCESS FOR THE PREPARATION OF SMALL MOLECULE INHIBITORS OF MDM2 AND INTERMEDIATES USED THEREIN THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2013-01-31 — — US claimed
US-12569564-B2 Spirocyclic MDM2 modulator and uses thereof NEWAVE PHARMACEUTICAL INC. (US) 2026-03-10 — — US disclosed
US-20250073340-A1 SPIROCYCLIC MDM2 MODULATOR AND USES THEREOF NEWAVE PHARMACEUTICAL INC. 2025-03-06 — — US disclosed
EP-4405359-A2 MDM2 DEGRADERS AND USES THEREOF Kymera Therapeutics, Inc. (US) 2024-07-31 — — EP disclosed
EP-3498712-B1 SPIROCYCLIC INDOLONE POLYETHYLENE GLYCOL CARBONATE COMPOUND, COMPOSITION, PREPARATION METHOD AND USE THEREOF JIANGSU YAYO BIOTECHNOLOGY CO LTD (CN) 2024-01-03 — — EP disclosed
US-11787814-B2 Method for preparing 2-indolinospirone compound and intermediate thereof ASCENTAGE PHARMA (SUZHOU) CO., LTD. (CN) 2023-10-17 — — US disclosed
US-11787814-B2 Method for preparing 2-indolinospirone compound and intermediate thereof ASCENTAGE PHARMA (SUZHOU) CO., LTD. (CN) 2023-10-17 — — US disclosed
EP-3183255-B1 SPIROPYRROLIDINES AS MDM2 INHIBITORS HUDSON BIOPHARMA INC (US) 2023-07-05 — — EP disclosed
WO-2023049790-A2 MDM2 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. (US) 2023-03-30 — — WO disclosed
CN-113387957-B Spirocyclic indolone-pyrrolidine carbonate compound and composition, preparation method and application thereof 江苏亚尧生物科技有限公司 2022-08-09 — — CN disclosed
WO-2011134925-A1 SPIROINDOLINONE PYRROLIDINES F. HOFFMANN-LA ROCHE AG (CH) 2011-11-03 — — WO disclosed
WO-2011067185-A1 SPIROINDOLINONE PYRROLIDINES F. HOFFMANN-LA ROCHE AG (CH) 2011-06-09 — — WO disclosed
US-20110130398-A1 SPIROINDOLINONE PYRROLIDINES BARTKOVITZ DAVID JOSEPH 2011-06-02 — — US disclosed
US-20100273799-A1 SMALL MOLECULE INHIBITORS OF MDM2 AND THE USES THEREOF THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2010-10-28 — — US disclosed
US-7759383-B2 INHIBITORS OF MURINE DOUBLE MINUTE-2(MDM2) SUCH AS (2'R,3'S,4'R,5'R)6-CHLORO-4'-2,2-DIMETHYL-PROPYL-2'-(2,2-DIMETHYL-PROPYL)-2-OXO-1,2-DIHYDRO-SPIRO[INDOLE-3,3'-PYRROLIDINE]-5'-CARBOXYLIC ACID(3-MORPHOLIN-4-YL-PROPYL)-AMIDE, USED FOR INDUCING APOPTOSIS AND CELL CYCLE ARREST; ANTIPROLIFERATIVE AGENTS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2010-07-20 — — US disclosed
US-7638548-B2 Spiroindolinone derivatives HOFFMANN-LA ROCHE INC. (US) 2009-12-29 — — US disclosed
US-20080114013-A1 SPIROINDOLINONE DERIVATIVES LIU JIN-JUN 2008-05-15 — — US disclosed
WO-2008055812-A1 SPIROINDOLINONE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2008-05-15 — — WO disclosed
US-20060211757-A1 INHIBITORS OF MURINE DOUBLE MINUTE-2(MDM2) SUCH AS (2'R,3'S,4'R,5'R)6-CHLORO-4'-2,2-DIMETHYL-PROPYL-2'-(2,2-DIMETHYL-PROPYL)-2-OXO-1,2-DIHYDRO-SPIRO[INDOLE-3,3'-PYRROLIDINE]-5'-CARBOXYLIC ACID(3-MORPHOLIN-4-YL-PROPYL)-AMIDE, USED FOR INDUCING APOPTOSIS AND CELL CYCLE ARREST; ANTIPROLIFERATIVE AGENTS REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2006-09-21 — — 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 (8 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-11787814-B2 Method for preparing 2-indolinospirone compound and intermediate thereof CYP51A1, CYP11B2, CYP3A5 MDM2 782/4885TUBB4A 3112/4885TUBB 3773/4885
US-20250073340-A1 SPIROCYCLIC MDM2 MODULATOR AND USES THEREOF FOXM1, MDM2, FOXO1 MDM2 2/4885TUBB4A 1863/4885TUBB 1576/4885
US-12569564-B2 Spirocyclic MDM2 modulator and uses thereof MDM2, TP53, XIAP MDM2 1/4885TUBB4A 2773/4885TUBB 2433/4885
US-20100273799-A1 SMALL MOLECULE INHIBITORS OF MDM2 AND THE USES THEREOF TP53, MDM2, CDKN1A MDM2 2/4885TUBB4A 2387/4885TUBB 2030/4885
US-20130030173-A1 PROCESS FOR THE PREPARATION OF SMALL MOLECULE INHIBITORS OF MDM2 AND INTERMEDIATES USED THEREIN TP53, MDM2, CDKN1A MDM2 2/4885TUBB4A 2763/4885TUBB 2280/4885
US-20080114013-A1 SPIROINDOLINONE DERIVATIVES RB1, XPOT, PDK2 MDM2 631/4885TUBB4A 292/4885TUBB 487/4885
US-20060211757-A1 INHIBITORS OF MURINE DOUBLE MINUTE-2(MDM2) SUCH AS (2'R,3'S,4'R,5'R)6-CHLORO-4'-2,2-DIMETHYL-PROPYL-2'-(2,2-DIMETHYL-PROPYL)-2-OXO-1,2-DIHYDRO-SPIRO[INDOLE-3,3'-PYRROLIDINE]-5'-CARBOXYLIC ACID(3-MORPHOLIN-4-YL-PROPYL)-AMIDE, USED FOR INDUCING APOPTOSIS AND CELL CYCLE ARREST; ANTIPROLIFERATIVE AGENTS SKP2, MDM2, CCAR2 MDM2 2/4885TUBB4A 2514/4885TUBB 2000/4885
US-20110130398-A1 SPIROINDOLINONE PYRROLIDINES RPS4Y1, RB1, RPS4X MDM2 1419/4885TUBB4A 1476/4885TUBB 1523/4885

“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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