SCHEMBL7789904

SCHEMBL7789904

COC(=O)CC1=C(C)Cc2ccc(F)cc21

nearest known ligand 0.35

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PPARG P37231 4/20 0.35
ALDH1A1 P00352 3/20 0.35
GAA P10253 2/20 0.35
KDM4E B2RXH2 1/20 0.35
CASP3 P42574 2/20 0.35
MAPT P10636 2/20 0.35
HTT P42858 1/20 0.35
RXRA P19793 1/20 0.34
MEN1 O00255 1/20 0.34
KMT2A Q03164 1/20 0.34
HTR7 P34969 1/20 0.34
MAPK14 Q16539 2/20 0.34
HSP90AB1 P08238 1/20 0.34
ACHE P22303 1/20 0.34
CA12 O43570 1/20 0.34
CA2 P00918 1/20 0.34
CA7 P43166 1/20 0.34
CA9 Q16790 1/20 0.34
CA14 Q9ULX7 1/20 0.34
PDK2 Q15119 1/20 0.34

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
SCHEMBL2586594 0.88 LMNA (0.38) PPARGMAPTRXRAMEN1KMT2A
SCHEMBL6936638 0.86 HSP90AB1 (0.36) ALDH1A1GAAMAPTHTTMEN1
SCHEMBL6938641 0.84 HSP90AB1 (0.41) ALDH1A1GAAKDM4EHSP90AB1
SCHEMBL1387817 0.84 PPARG (0.49) PPARGALDH1A1KDM4EMAPTRXRA
SCHEMBL6933096 0.83 METAP1 (0.44) PPARG
SCHEMBL17853664 0.83 PPARG (0.36) PPARGALDH1A1KDM4EMAPTRXRA
SCHEMBL3862066 0.83 PPARG (0.36) PPARGMAPTRXRAKMT2AACHE
SCHEMBL28794754 0.81 ALDH1A1 (0.47) PPARGALDH1A1RXRAL3MBTL1LMNA
SCHEMBL6932963 0.81 GAA (0.40) GAAHTTKMT2AHSP90AB1LMNA
SCHEMBL6931403 0.81 HPGD (0.34) ALDH1A1GAAKDM4EMAPTHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102030642-A Synthesis method and application of intermediate of sulindac analogue UNIV XIAMEN 2011-04-27 CN disclosed
US-20010020020-A1 Method for treating patients with macular degeneration by administering substituted sulfonyl indenyl acetic acids and alcohols PAMUKCU RIFAT (US) 2001-09-06 US disclosed
US-20010006965-A1 Method for treating patients with diabetic retinopathy by administering substituted sulfonyl indenyl acetic acids and alcohols PAMUKCU RIFAT (US) 2001-07-05 US disclosed
US-6177471-B1 PHOSPHODIESTERASE INHIBITOR CELL PATHWAYS, INC. 2001-01-23 US disclosed
US-6028116-A Substituted condensation products of 1H-indenyl-hydroxyalkanes with aldehydes for neoplasia CELL PATHWAYS, INC. (US) 2000-02-22 US disclosed
US-6025394-A Method for treating patients with acne by administering substituted sulfonyl indenyl acetic acids, amides and alcohols CELL PATHWAYS, INC. (US) 2000-02-15 US disclosed
US-5965619-A ADMINISTERING AN INDENE DERIVATIVE OF GIVEN FORMULA, SUCH AS 1-(2,4,6-TRIMETHOXYBENZYLIDENE)-5-DIMETHYLAMINO-2-METHYL-3-INDENYL ACETIC ACID, TO TREAT PRECANCEROUS LESIONS SUCH AS COLONIC ADENOMATOUS POLYPS; SIDE EFFECT REDUCTION CELL PATHWAYS INC. (US) 1999-10-12 US disclosed
US-5958982-A Method for treating patients with sarcoidosis by administering substituted sulfonyl indenyl acetic acids, esters and alcohols CELL PATHWAYS, INC. (US) 1999-09-28 US disclosed
US-5902827-A Method for treating patients with psoriasis by administering substituted sulfonyl indenyl acetic acids, esters and alcohols CELL PATHWAYS (US) 1999-05-11 US disclosed
EP-0206241-B1 PROCESS FOR THE PREPARATION OF CIS-5-FLUORO-2-METHYL-1-(4-METHYLTHIOBENZYLIDENE)-INDENE-3-ACETIC ACID ZAMBON S.p.A. (IT) 1989-04-19 EP disclosed
US-4748271-A Process for the preparation of cis-5-fluoro-2-methyl-1-(4-methyl-thiobenzylidene)-indene-3-acetic acid ZAMBON S.P.A. (IT) 1988-05-31 US disclosed
US-4656190-A PLATELET ACTIVATING FACTOR MERCK & CO., INC. (US) 1987-04-07 US disclosed
EP-0206241-A1 Process for the preparation of cis-5-fluoro-2-methyl-1-(4-methylthiobenzylidene)-indene-3-acetic acid ZAMBON S.p.A. (IT) 1986-12-30 EP disclosed
EP-0142801-A2 Indene derivatives useful as paf-antagonists MERCK & CO. INC. (US) 1985-05-29 EP 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-20010020020-A1 Method for treating patients with macular degeneration by administering substituted sulfonyl indenyl acetic acids and alcohols ALDH1A2, ALDH1A3, FFAR3 PPARG 31/4885ALDH1A1 13/4885GAA 3425/4885
US-20010006965-A1 Method for treating patients with diabetic retinopathy by administering substituted sulfonyl indenyl acetic acids and alcohols ALDH1A2, ALDH1A3, IAPP PPARG 32/4885ALDH1A1 25/4885GAA 2390/4885

“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.