SCHEMBL2735680

SCHEMBL2735680

Cc1cccc(NC(=O)C(C)C)c1

nearest known ligand 0.65

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 1/20 0.65
SMN1; SMN2 Q16637 5/20 0.63
LMNA P02545 1/20 0.63
KMT2A Q03164 4/20 0.59
MEN1 O00255 3/20 0.59
RXFP1 Q9HBX9 2/20 0.59
ALDH1A1 P00352 2/20 0.56
MAPT P10636 1/20 0.56
F2R P25116 1/20 0.55
L3MBTL1 Q9Y468 1/20 0.55
KCNK3 O14649 1/20 0.54
KCNH2 Q12809 1/20 0.54
KCNK9 Q9NPC2 1/20 0.54
PKM P14618 1/20 0.54
HPGD P15428 1/20 0.54
NPC1 O15118 1/20 0.54
RAB9A P51151 1/20 0.54

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
SCHEMBL30729659 0.87 HSD17B10 (0.62) HSD17B10SMN1; SMN2KMT2AMEN1RXFP1
SCHEMBL20152029 0.86 HSD17B10 (0.61) HSD17B10SMN1; SMN2KMT2AMEN1RXFP1
SCHEMBL4820385 0.86 HSD17B10 (0.61) HSD17B10SMN1; SMN2KMT2AMEN1RXFP1
SCHEMBL12812735 0.86 HSD17B10 (0.61) HSD17B10SMN1; SMN2KMT2AMEN1RXFP1
SCHEMBL4003494 0.86 HSD17B10 (0.61) HSD17B10SMN1; SMN2KMT2AMEN1RXFP1
SCHEMBL26464127 0.86 HSD17B10 (0.61) HSD17B10SMN1; SMN2KMT2AMEN1RXFP1
SCHEMBL11866935 0.85 SMN1; SMN2 (0.63) SMN1; SMN2LMNAKMT2AMEN1RXFP1
SCHEMBL6429391 0.84 HSD17B10 (0.64) HSD17B10SMN1; SMN2KMT2AMEN1RXFP1
SCHEMBL13255714 0.84 HSD17B10 (0.59) HSD17B10SMN1; SMN2KMT2AMEN1RXFP1
SCHEMBL17896778 0.84 HSD17B10 (0.62) HSD17B10SMN1; SMN2KMT2AMEN1RXFP1

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-10752617-B2 Indazole sulfonamide derivatives as inverse agonists of retinoid-related orphan receptor gamma (ROR gamma (T)) GALDERMA RESEARCH & DEVELOPMENT (FR) 2020-08-25 US claimed
EP-3233836-B1 INDAZOLE SULFONAMIDE DERIVATIVES AS INVERSE AGONISTS OF RETINOID-RELATED ORPHAN RECEPTOR GAMMA (ROR GAMMA (T)) GALDERMA RES & DEV (FR) 2019-01-30 EP claimed
US-11826365-B2 Type II raf kinase inhibitors DANA-FARBER CANCER INSTITUTE, INC. (US) 2023-11-28 US disclosed
US-11827640-B2 Substituted pyrazolo[1,5-a]pyrimidines as CFTR modulators ILDONG PHARMACEUTICAL CO., LTD. (KR) 2023-11-28 US disclosed
US-20230242514-A1 BICYCLIC INDAZOLE GLUCOCORTICOID RECEPTOR ANTAGONISTS CORCEPT THERAPEUTICS INCORPORATED 2023-08-03 US disclosed
US-20230242514-A1 BICYCLIC INDAZOLE GLUCOCORTICOID RECEPTOR ANTAGONISTS CORCEPT THERAPEUTICS INCORPORATED 2023-08-03 US disclosed
US-11680074-B2 Compounds, functionalised dioxaborolane or dioxaborinane derivatives, method for preparing same and uses thereof ECOLE SUPERIEURE DE PHYSIQUE ET DE CHIMIE INDUSTRIELLES DE LA VILLE DE PARIS (FR) 2023-06-20 US disclosed
WO-2022271970-A1 METHODS AND COMPOSITIONS USEFUL FOR NUCLEIC ACID SEQUENCING Singular Genomics Systems, Inc. (US) 2022-12-29 WO disclosed
WO-2022169755-A1 SULFONAMIDE SUBSTITUTED N-(1H-INDOL-7-YL) BENZENESULFONAMIDES AND USES THEREOF TRIANA BIOMEDICINES, INC. (US) 2022-08-11 WO disclosed
EP-3464300-B1 NOVEL COMPOUNDS, FUNCTIONALISED DIOXABOROLANE OR DIOXABORINANE DERIVATIVES, METHOD FOR PREPARING SAME AND USES THEREOF ECOLE SUPERIEURE DE PHYSIQUE ET CHIMIE IND DE LA VILLE DE PARIS (FR) 2021-12-01 EP disclosed
US-10752617-B2 Indazole sulfonamide derivatives as inverse agonists of retinoid-related orphan receptor gamma (ROR gamma (T)) GALDERMA RESEARCH & DEVELOPMENT (FR) 2020-08-25 US disclosed
US-20110065700-A1 POLYSUBSTITUTED DERIVATIVES OF 6-HETEROARYLIMIDAZO[1,2-a]PYRIDINES, AND PREPARATION AND THERAPEUTIC USE THEREOF SANOFI-AVENTIS (FR) 2011-03-17 US disclosed
US-20100305100-A1 METHODS FOR TREATING HEPATITIS C PTC THERAPEUTICS, INC. (US) 2010-12-02 US disclosed
US-20100292187-A1 METHODS FOR TREATING HEPATITIS C PTC THERAPEUTICS, INC. (US) 2010-11-18 US disclosed
CN-101663262-A N- (3-benzyl) -2, 2- (diphenyl) -propan-1-amine derivatives as CETP inhibitors for the treatment of atherosclerosis and cardiovascular diseases BRISTOL MYERS SQUIBB CO 2010-03-03 CN disclosed
US-7550458-B2 Tricycloundecane compounds useful as modulators of nuclear hormone receptor function BRISTOL-MYERS SQUIBB COMPANY (US) 2009-06-23 US disclosed
US-20070088029-A1 Tricycloundecane compounds useful as modulators of nuclear hormone receptor function BRISTOL-MYERS SQUIBB COMPANY 2007-04-19 US disclosed
US-20070078146-A1 Antiinflamamtory agents; antiarthritic agents; inflammatory bowel disorders; multiple sclerosis; asthma PHARMACIA CORPORATION 2007-04-05 US disclosed
WO-2003043630-A1 SOLID PHARMACEUTICAL COMPOSITION COMPRISING 4-CYANO-TRIFLUORO-3-(4-FLUOROPHENYL SULPHONYL)-2-HYDROXY-2-METHYLPROPIONO- M TOLUIDIDE, PVP, AN ANTI-OESTROGEN AND/OR AN AROMATASE INHIBITOR ASTRAZENECA UK LIMITED (GB) 2003-05-30 WO disclosed
US-4302599-A Process for nitrating anilides SCHERING CORPORATION (US) 1981-11-24 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 (10 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-11827640-B2 Substituted pyrazolo[1,5-a]pyrimidines as CFTR modulators PDE4A, PDE4B, PDE5A HSD17B10 3013/4885SMN1; SMN2 3416/4885LMNA 4118/4885
US-11680074-B2 Compounds, functionalised dioxaborolane or dioxaborinane derivatives, method for preparing same and uses thereof RDX, XDH, NOX4 HSD17B10 1150/4885SMN1; SMN2 3745/4885LMNA 1743/4885
US-20110065700-A1 POLYSUBSTITUTED DERIVATIVES OF 6-HETEROARYLIMIDAZO[1,2-a]PYRIDINES, AND PREPARATION AND THERAPEUTIC USE THEREOF CYP4X1, HAX1, JAK2 HSD17B10 2045/4885SMN1; SMN2 3292/4885LMNA 3699/4885
US-11826365-B2 Type II raf kinase inhibitors BRAF, RAF1, ARAF HSD17B10 2379/4885SMN1; SMN2 2691/4885LMNA 3146/4885
US-20100292187-A1 METHODS FOR TREATING HEPATITIS C HAVCR2, EIF2AK2, MAVS HSD17B10 1276/4885SMN1; SMN2 3609/4885LMNA 1012/4885
US-10752617-B2 Indazole sulfonamide derivatives as inverse agonists of retinoid-related orphan receptor gamma (ROR gamma (T)) RORA, RORB, RORC HSD17B10 818/4885SMN1; SMN2 4627/4885LMNA 4400/4885
US-20070078146-A1 Antiinflamamtory agents; antiarthritic agents; inflammatory bowel disorders; multiple sclerosis; asthma MAPK1, MAPK3, MAPK4 HSD17B10 4567/4885SMN1; SMN2 2049/4885LMNA 4386/4885
US-20230242514-A1 BICYCLIC INDAZOLE GLUCOCORTICOID RECEPTOR ANTAGONISTS NR3C1, NR3C2, NR1I2 HSD17B10 692/4885SMN1; SMN2 4370/4885LMNA 4289/4885
US-20100305100-A1 METHODS FOR TREATING HEPATITIS C HAVCR2, EIF2AK2, MAVS HSD17B10 1276/4885SMN1; SMN2 3609/4885LMNA 1012/4885
US-20070088029-A1 Tricycloundecane compounds useful as modulators of nuclear hormone receptor function VDR, ESRRB, NR5A1 HSD17B10 94/4885SMN1; SMN2 4802/4885LMNA 3299/4885

“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.