SCHEMBL2241703

SCHEMBL2241703

CC1=C(Nc2ccc(S(=O)(=O)NC(=O)c3ccccc3)cc2)C(=O)c2ccccc2C1=O

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KMT2A Q03164 4/20 0.64
▸ MEN1 O00255 3/20 0.64
▸ LMNA P02545 6/20 0.53
▸ L3MBTL1 Q9Y468 5/20 0.53
▸ FLT1 P17948 1/20 0.53
▸ FLT4 P35916 1/20 0.53
▸ KDR P35968 1/20 0.53
▸ HTT P42858 4/20 0.51
▸ MAPT P10636 5/20 0.50
▸ MAPK1 P28482 4/20 0.50
▸ APAF1 O14727 3/20 0.50
▸ MITF O75030 2/20 0.50
▸ KDM4E B2RXH2 1/20 0.50
▸ POLB P06746 1/20 0.50
▸ SMN1; SMN2 Q16637 1/20 0.50
▸ TDP1 Q9NUW8 3/20 0.47
▸ MCL1 Q07820 3/20 0.47
▸ ALDH1A1 P00352 2/20 0.47
▸ TP53 P04637 2/20 0.47
▸ HPGD P15428 2/20 0.47

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
SCHEMBL2246287 0.85 MAPT (0.64) KMT2AMEN1LMNAL3MBTL1FLT1
SCHEMBL2244803 0.79 RAB9A (0.59) KMT2AMEN1LMNAL3MBTL1FLT1
SCHEMBL14585676 0.77 FLT1 (0.67) KMT2AMEN1LMNAL3MBTL1FLT1
SCHEMBL5931087 0.76 PTGS2 (0.71) KMT2AMEN1LMNAL3MBTL1FLT1
SCHEMBL3292237 0.75 PTGS2 (0.69) KMT2AMEN1LMNAL3MBTL1FLT1
SCHEMBL9967797 0.74 CA1 (0.64) KMT2AMEN1LMNAL3MBTL1FLT1
SCHEMBL174010 0.74 FLT1 (0.77) KMT2AMEN1LMNAL3MBTL1FLT1
SCHEMBL18456985 0.74 MEN1 (0.71) KMT2AMEN1LMNAL3MBTL1FLT1
SCHEMBL7774524 0.74 LMNA (0.72) KMT2AMEN1LMNAL3MBTL1FLT1
SCHEMBL12354484 0.74 MMP2 (0.61) KMT2AMEN1LMNAL3MBTL1FLT1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8673910-B2 Proteasome inhibitors for selectively inducing apoptosis in cancer cells H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE (US) 2014-03-18 — — US disclosed
US-8673910-B2 Proteasome inhibitors for selectively inducing apoptosis in cancer cells H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE (US) 2014-03-18 — — US disclosed
US-8673910-B2 Proteasome inhibitors for selectively inducing apoptosis in cancer cells H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE (US) 2014-03-18 — — US disclosed
US-20110201609-A1 PROTEASOME INHIBITORS FOR SELECTIVELY INDUCING APOPTOSIS IN CANCER CELLS H. LEE MOFFITT CANCER CENTER & RESEARCH INSTITUTE (US) 2011-08-18 — — US disclosed
US-20110201609-A1 PROTEASOME INHIBITORS FOR SELECTIVELY INDUCING APOPTOSIS IN CANCER CELLS H. LEE MOFFITT CANCER CENTER & RESEARCH INSTITUTE (US) 2011-08-18 — — US disclosed
US-20110201609-A1 PROTEASOME INHIBITORS FOR SELECTIVELY INDUCING APOPTOSIS IN CANCER CELLS H. LEE MOFFITT CANCER CENTER & RESEARCH INSTITUTE (US) 2011-08-18 — — US disclosed
WO-2010005534-A2 PROTEASOME INHIBITORS FOR SELECTIVELY INDUCING APOPTOSIS IN CANCER CELLS H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. (US) 2010-01-14 — — 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 (1 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-20110201609-A1 PROTEASOME INHIBITORS FOR SELECTIVELY INDUCING APOPTOSIS IN CANCER CELLS PSMB7, PSMD7, PSMB6 KMT2A 2094/4885MEN1 4575/4885LMNA 2096/4885

“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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