SCHEMBL7647937

SCHEMBL7647937

CC(C)(C(=O)O)[C@](O)(C(=O)O)[C@](C)(O)C(=O)O

nearest known ligand 0.45

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 2/20 0.45
▸ ALDH1A1 P00352 1/20 0.45
▸ HMGCR P04035 1/20 0.32
▸ CHRM1 P11229 1/20 0.32
▸ TBXA2R P21731 1/20 0.32
▸ ADRA1A P35348 1/20 0.32
▸ CYP2D6 P10635 1/20 0.31
▸ CYP2C19 P33261 1/20 0.31
▸ HIF1A Q16665 1/20 0.31
▸ TET2 Q6N021 1/20 0.30

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
SCHEMBL27667108 0.85 TSHR (0.53) TSHRALDH1A1HMGCRCHRM1TBXA2R
SCHEMBL3112519 0.79 TSHR (0.53) TSHRALDH1A1HMGCRCHRM1TBXA2R
SCHEMBL10453248 0.75 ALDH1A1 (0.64) TSHRALDH1A1HMGCRCHRM1TBXA2R
SCHEMBL10472538 0.75 ALDH1A1 (0.64) TSHRALDH1A1HMGCRCHRM1TBXA2R
SCHEMBL606619 0.75 ALDH1A1 (0.64) TSHRALDH1A1HMGCRCHRM1TBXA2R
SCHEMBL14996042 0.74 ALDH1A1 (0.41) TSHRALDH1A1
SCHEMBL811208 0.72 ALDH1A1 (0.39) TSHRALDH1A1
SCHEMBL85493 0.71 TSHR (0.57) TSHRALDH1A1HMGCRCHRM1TBXA2R
SCHEMBL3993905 0.69 TSHR (0.56) TSHRALDH1A1HMGCRCHRM1TBXA2R
SCHEMBL1195464 0.69 TSHR (0.56) TSHRALDH1A1HMGCRCHRM1TBXA2R

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-6489493-B2 ESTERIFYING HIBISCUS ACID WITH AN ALCOHOL IN PRESENCE OF AN INORGANIC CATALYST; NEUTRALIZATION; CONCENTRATION BY EVAPORATION; SOLVENT EXTRACTION DEPARTMENT OF SCIENCE AND TECHNOLOGY, TECHNOLOGY BHAVAN (IN) 2002-12-03 — — US claimed
US-6489493-B2 ESTERIFYING HIBISCUS ACID WITH AN ALCOHOL IN PRESENCE OF AN INORGANIC CATALYST; NEUTRALIZATION; CONCENTRATION BY EVAPORATION; SOLVENT EXTRACTION DEPARTMENT OF SCIENCE AND TECHNOLOGY, TECHNOLOGY BHAVAN (IN) 2002-12-03 — — US disclosed
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