SCHEMBL22466974

SCHEMBL22466974

c1n[nH]cc1-c1nc2ccc3[nH]ncc3c2c2c1CCCC2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ FLT3 P36888 18/20 1.00
▸ CDK2 P24941 17/20 1.00
▸ CCNA1 P78396 17/20 1.00
▸ STING1 Q86WV6 1/20 1.00
▸ CCNT1 O60563 1/20 0.65
▸ CDK1 P06493 1/20 0.65
▸ CCNB1 P14635 1/20 0.65
▸ CCNA2 P20248 1/20 0.65
▸ CCNE1 P24864 1/20 0.65
▸ CDK9 P50750 1/20 0.65
▸ PBK Q96KB5 1/20 0.61
▸ HASPIN Q8TF76 2/20 0.58
▸ ROCK2 O75116 1/20 0.53
▸ ROCK1 Q13464 1/20 0.53

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
SCHEMBL30490739 1.00 FLT3 (1.00) FLT3CDK2CCNA1STING1CCNT1
SCHEMBL31123096 0.99 FLT3 (0.98) FLT3CDK2CCNA1STING1CCNT1
SCHEMBL31123088 0.97 FLT3 (0.95) FLT3CDK2CCNA1STING1CCNT1
SCHEMBL22477939 0.86 FLT3 (0.76) FLT3CDK2CCNA1STING1CCNT1
SCHEMBL31123110 0.86 CDK2 (0.75) FLT3CDK2CCNA1STING1CCNT1
SCHEMBL22467149 0.85 FLT3 (0.74) FLT3CDK2CCNA1STING1CCNT1
SCHEMBL31123084 0.85 CDK2 (0.73) FLT3CDK2CCNA1STING1CCNT1
SCHEMBL22466864 0.84 FLT3 (0.72) FLT3CDK2CCNA1STING1CCNT1
SCHEMBL22478078 0.84 FLT3 (0.72) FLT3CDK2CCNA1STING1CCNT1
SCHEMBL22478080 0.84 FLT3 (0.72) FLT3CDK2CCNA1STING1CCNT1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4688157-A1 3H-PYRAZOLO[4.3:f] QUINOLINE-BASED COMPOUNDS AS STING ANTAGONISTS Purdue Research Foundation (US) 2026-02-11 — — EP disclosed
US-12384782-B2 Inhibitors of kinase networks and uses thereof PURDUE RESEARCH FOUNDATION (US) 2025-08-12 — — US disclosed
WO-2024206164-A1 3H-PYRAZOLO[4.3:f] QUINOLINE-BASED COMPOUNDS AS STING ANTAGONISTS PURDUE RESEARCH FOUNDATION (US) 2024-10-03 — — WO disclosed
US-20240208971-A1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF PURDUE RESEARCH FOUNDATION 2024-06-27 — — US disclosed
US-11891391-B2 Inhibitors of kinase networks and uses thereof PURDUE RESEARCH FOUNDATION (US) 2024-02-06 — — US disclosed
EP-4233859-A1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF Purdue Research Foundation (US) 2023-08-30 — — EP disclosed
EP-4233859-A1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF Purdue Research Foundation (US) 2023-08-30 — — EP disclosed
EP-3600287-B1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF PURDUE RESEARCH FOUNDATION (US) 2023-07-05 — — EP disclosed
EP-3600287-B1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF PURDUE RESEARCH FOUNDATION (US) 2023-07-05 — — EP disclosed
CN-110662536-B Kinase network inhibitors and uses thereof 普渡研究基金会 2023-06-23 — — CN disclosed
US-20210371420-A1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF PURDUE RESEARCH FOUNDATION 2021-12-02 — — US disclosed
US-20210371420-A1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF PURDUE RESEARCH FOUNDATION 2021-12-02 — — US disclosed
US-11040973-B2 Inhibitors of kinase networks and uses thereof PURDUE RESEARCH FOUNDATION 2021-06-22 — — US disclosed
US-11040973-B2 Inhibitors of kinase networks and uses thereof PURDUE RESEARCH FOUNDATION 2021-06-22 — — US disclosed
US-20200308173-A1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF PURDUE RESEARCH FOUNDATION 2020-10-01 — — US disclosed
US-20200308173-A1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF PURDUE RESEARCH FOUNDATION 2020-10-01 — — US disclosed
CN-110662536-A Kinase network inhibitors and uses thereof 普渡研究基金会 2020-01-07 — — CN 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-20200308173-A1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF KDM1B, JMJD6, KDM1A FLT3 556/4885CDK2 308/4885CCNA1 2225/4885
US-11040973-B2 Inhibitors of kinase networks and uses thereof KDM1B, JMJD6, KDM1A FLT3 556/4885CDK2 308/4885CCNA1 2225/4885
US-12384782-B2 Inhibitors of kinase networks and uses thereof KDM1B, JMJD6, KDM1A FLT3 556/4885CDK2 308/4885CCNA1 2225/4885
US-20210371420-A1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF KDM1B, JMJD6, KDM1A FLT3 556/4885CDK2 308/4885CCNA1 2225/4885
US-20240208971-A1 INHIBITORS OF KINASE NETWORKS AND USES THEREOF KDM1B, JMJD6, KDM1A FLT3 556/4885CDK2 308/4885CCNA1 2225/4885
US-11891391-B2 Inhibitors of kinase networks and uses thereof KDM1B, JMJD6, KDM1A FLT3 556/4885CDK2 308/4885CCNA1 2225/4885

“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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