SCHEMBL8837048

SCHEMBL8837048

CC(C)CCC[C@@H](C)[C@H]1C[C@@H]2O[C@@]23C2=CC[C@H]4C[C@@H](OC(=O)c5ccccc5)CC[C@]4(C)[C@H]2CC[C@]13C

nearest known ligand 0.42

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ MEN1 O00255 1/20 0.42
▸ USP2 O75604 1/20 0.42
▸ ALDH1A1 P00352 1/20 0.42
▸ MAPT P10636 1/20 0.42
▸ ALOX15 P16050 1/20 0.42
▸ KMT2A Q03164 1/20 0.42
▸ HMGCR P04035 2/20 0.41
▸ DHCR24 Q15392 9/20 0.41
▸ CDC25A P30304 3/20 0.40
▸ CXCR1 P25024 1/20 0.40
▸ LMNA P02545 1/20 0.39
▸ TDP1 Q9NUW8 1/20 0.39
▸ POLA1 P09884 2/20 0.38
▸ PTGES O14684 1/20 0.36
▸ SLC10A2 Q12908 1/20 0.36
▸ SLC10A1 Q14973 1/20 0.36

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
SCHEMBL9350364 1.00 MEN1 (0.42) MEN1USP2ALDH1A1MAPTALOX15
SCHEMBL9164370 1.00 MEN1 (0.42) MEN1USP2ALDH1A1MAPTALOX15
SCHEMBL10587792 1.00 MEN1 (0.42) MEN1USP2ALDH1A1MAPTALOX15
SCHEMBL10424858 1.00 MEN1 (0.42) MEN1USP2ALDH1A1MAPTALOX15
SCHEMBL10587788 1.00 MEN1 (0.42) MEN1USP2ALDH1A1MAPTALOX15
SCHEMBL9769614 0.87 HMGCR (0.46) MEN1USP2ALDH1A1MAPTALOX15
SCHEMBL9353906 0.87 MEN1 (0.43) MEN1USP2ALDH1A1MAPTALOX15
SCHEMBL11412835 0.84 MEN1 (0.42) MEN1USP2ALDH1A1MAPTALOX15
SCHEMBL11411951 0.84 MEN1 (0.42) MEN1USP2ALDH1A1MAPTALOX15
SCHEMBL11411677 0.84 MEN1 (0.42) MEN1USP2ALDH1A1MAPTALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0327119-B1 Improved process for synthesis of 5-alpha-cholest-8(14)-en-3 beta-ol-15-one and other 15-oxygenated sterols UNIV RICE WILLIAM M (US) 1994-09-14 — — EP claimed
US-4900477-A Novel intermediates and an improved process for producing the compound (3β,5α)-3-hydroxycholest-8(14)-en-15-one AMERICAN CYANAMID COMPANY (US) 1990-02-13 — — US claimed
US-4897475-A OXYGENATION OF 7-DEHYDROCHOLESTEROL WILLIAM MARSH RICE UNIVERSITY (US) 1990-01-30 — — US claimed
EP-0335106-A2 Novel intermediates and an improved process for producing the compound (3 beta, 5 alpha)-3-hydroxycholest-8(14)-en-15-one AMERICAN CYANAMID COMPANY (US) 1989-10-04 — — EP claimed
EP-0327119-A2 Improved process for synthesis of 5-alpha-cholest-8(14)-en-3 beta-ol-15-one and other 15-oxygenated sterols WILLIAM MARSH RICE UNIVERSITY (US) 1989-08-09 — — EP claimed
US-5688780-A ANTICHOLESTEROL AGENTS, CHOLESTEROL BIOSYNTHESIS INHIBITION SRI INTERNATIONAL (US) 1997-11-18 — — US disclosed
US-5510340-A OXYSTEROL ANALOGS SRI INTERNATIONAL (US) 1996-04-23 — — US disclosed
EP-0644891-A1 ANTIHYPERCHOLESTEROLEMIC COMPOUNDS AND RELATED PHARMACEUTICAL COMPOSITIONS AND METHODS OF USE SRI INTERNATIONAL (US) 1995-03-29 — — EP disclosed
WO-1993025568-A2 ANTIHYPERCHOLESTEROLEMIC COMPOUNDS AND RELATED PHARMACEUTICAL COMPOSITIONS AND METHODS OF USE SRI INTERNATIONAL (US) 1993-12-23 — — WO disclosed
US-4900477-A Novel intermediates and an improved process for producing the compound (3β,5α)-3-hydroxycholest-8(14)-en-15-one AMERICAN CYANAMID COMPANY (US) 1990-02-13 — — US disclosed
US-4897475-A OXYGENATION OF 7-DEHYDROCHOLESTEROL WILLIAM MARSH RICE UNIVERSITY (US) 1990-01-30 — — US disclosed
EP-0335106-A2 Novel intermediates and an improved process for producing the compound (3 beta, 5 alpha)-3-hydroxycholest-8(14)-en-15-one AMERICAN CYANAMID COMPANY (US) 1989-10-04 — — EP disclosed
US-4202891-A ANOREXIGENIC AGENTS, ANTICHOLESTEROL AGENTS, INHIBITORS OF CELL GROWTH PARISH, EDWARD J. 1980-05-13 — — US disclosed
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