SCHEMBL26258736

SCHEMBL26258736

Cc1ccc2c(c1)C(c1ccc(Cl)cc1)=N[C@@H](CC(=O)NCc1ccccc1)c1nnc(C)n1-2

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ BRD4 O60885 13/20 0.73
▸ BRD2 P25440 4/20 0.73
▸ BRD3 Q15059 2/20 0.73
▸ HDAC1 Q13547 8/20 0.71
▸ HDAC2 Q92769 8/20 0.71
▸ HDAC3 O15379 7/20 0.71
▸ HDAC4 P56524 7/20 0.71
▸ HDAC7 Q8WUI4 7/20 0.71
▸ HDAC10 Q969S8 7/20 0.71
▸ HDAC11 Q96DB2 7/20 0.71
▸ HDAC8 Q9BY41 7/20 0.71
▸ HDAC6 Q9UBN7 7/20 0.71
▸ HDAC9 Q9UKV0 7/20 0.71
▸ HDAC5 Q9UQL6 7/20 0.71
▸ SMCHD1 A6NHR9 1/20 0.65
▸ MYO1G B0I1T2 1/20 0.65
▸ AIP O00170 1/20 0.65
▸ AP3B1 O00203 1/20 0.65
▸ PSMD11 O00231 1/20 0.65
▸ CDC7 O00311 1/20 0.65

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
SCHEMBL26258758 0.92 BRD4 (0.64) BRD4BRD2BRD3HDAC1HDAC2
SCHEMBL14756861 0.90 BRD4 (0.81) BRD4BRD2BRD3HDAC1HDAC2
SCHEMBL26258735 0.90 HDAC1 (0.65) BRD4BRD2BRD3HDAC1HDAC2
SCHEMBL29377764 0.90 BRD4 (0.81) BRD4BRD2BRD3HDAC1HDAC2
SCHEMBL26315418 0.90 HDAC1 (0.64) BRD4BRD2BRD3HDAC1HDAC2
SCHEMBL14756264 0.89 BRD4 (0.81) BRD4BRD2BRD3HDAC1HDAC2
SCHEMBL26258732 0.88 HDAC1 (0.70) BRD4BRD2BRD3HDAC1HDAC2
SCHEMBL26258737 0.86 BRD4 (0.67) BRD4BRD2BRD3HDAC1HDAC2
SCHEMBL26258756 0.86 HDAC1 (0.61) BRD4BRD2BRD3HDAC1HDAC2
SCHEMBL26258706 0.86 BRD4 (0.79) BRD4BRD2BRD3HDAC1HDAC2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230285570-A1 THERAPEUTICALLY USEFUL CURE-PRO MOLECULES FOR E3 LIGASE MEDIATED DEGRADATION OF PROTEINS, AND METHODS OF MAKING AND USING THEM CORNELL UNIVERSITY 2023-09-14 — — US disclosed
US-20230277553-A1 THERAPEUTIC COMPOSITION OF CURE-PRO COMPOUNDS FOR TARGETED DEGRADATION OF BET DOMAIN PROTEINS, AND METHODS OF MAKING AND USAGE CORNELL UNIVERSITY 2023-09-07 — — 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 (2 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-20230285570-A1 THERAPEUTICALLY USEFUL CURE-PRO MOLECULES FOR E3 LIGASE MEDIATED DEGRADATION OF PROTEINS, AND METHODS OF MAKING AND USING THEM XIAP, CUL4A, CUL1 BRD4 331/4885BRD2 497/4885BRD3 431/4885
US-20230277553-A1 THERAPEUTIC COMPOSITION OF CURE-PRO COMPOUNDS FOR TARGETED DEGRADATION OF BET DOMAIN PROTEINS, AND METHODS OF MAKING AND USAGE BET1, BRD4, PHKB BRD4 2/4885BRD2 12/4885BRD3 11/4885

“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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