SCHEMBL572198

SCHEMBL572198

C=C1C[C@@H]2[C@H](CC[C@@]3(C)[C@H]2CC[C@]3(O)C(C)=O)[C@@]2(C)CCC(=O)C=C12

nearest known ligand 0.72

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 8/20 0.67
▸ SHBG P04278 5/20 0.67
▸ NR3C1 P04150 4/20 0.67
▸ CYP2C19 P33261 3/20 0.67
▸ MEN1 O00255 3/20 0.67
▸ KMT2A Q03164 3/20 0.67
▸ SMN1; SMN2 Q16637 3/20 0.67
▸ SERPINA6 P08185 3/20 0.67
▸ MAPT P10636 2/20 0.67
▸ BLM P54132 2/20 0.67
▸ ADORA3 P0DMS8 1/20 0.67
▸ MAPK3 P27361 1/20 0.67
▸ SLC6A3 Q01959 1/20 0.67
▸ HIF1A Q16665 4/20 0.64
▸ PGR P06401 3/20 0.62
▸ AR P10275 2/20 0.62
▸ CHRM1 P11229 2/20 0.62
▸ CYP3A4 P08684 4/20 0.53
▸ HSD17B10 Q99714 3/20 0.53
▸ TSHR P16473 2/20 0.53

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
SCHEMBL13965592 1.00 LMNA (0.67) LMNASHBGNR3C1CYP2C19MEN1
SCHEMBL6693993 0.89 LMNA (0.53) LMNASHBGNR3C1CYP2C19MEN1
SCHEMBL6693991 0.89 LMNA (0.53) LMNASHBGNR3C1CYP2C19MEN1
SCHEMBL13518429 0.89 LMNA (0.70) LMNASHBGNR3C1CYP2C19MEN1
SCHEMBL295690 0.88 LMNA (0.51) LMNASHBGNR3C1CYP2C19MEN1
SCHEMBL9128581 0.86 SHBG (0.65) LMNASHBGNR3C1CYP2C19MEN1
SCHEMBL9128571 0.86 SHBG (0.65) LMNASHBGNR3C1CYP2C19MEN1
SCHEMBL11205039 0.86 NR3C1 (0.60) LMNASHBGNR3C1CYP2C19MEN1
SCHEMBL15079253 0.86 LMNA (0.49) LMNASHBGNR3C1CYP2C19MEN1
SCHEMBL10444770 0.86 LMNA (0.49) LMNASHBGNR3C1CYP2C19MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113583074-A Novel preparation method of 6-methyl-17 alpha-hydroxyprogesterone and precursor thereof 佳尔科生物科技南通有限公司 2021-11-02 — — CN claimed
CN-1294519-A Pharmaceutical composition containing a compound having an activity of promoting the absorption of an active ingredient INPHARMA SA (CH) 2001-05-09 — — CN claimed
CN-113583074-A Novel preparation method of 6-methyl-17 alpha-hydroxyprogesterone and precursor thereof 佳尔科生物科技南通有限公司 2021-11-02 — — CN disclosed
CN-113583074-A Novel preparation method of 6-methyl-17 alpha-hydroxyprogesterone and precursor thereof 佳尔科生物科技南通有限公司 2021-11-02 — — CN disclosed
US-20140234271-A1 COMPOSITIONS FOR PROLIFERATION OF CELLS AND RELATED METHODS THE HOSPITAL FOR SICK CHILDREN (CA) 2014-08-21 — — US disclosed
US-8748177-B2 Compositions for proliferation of cells and related methods THE HOSPITAL FOR SICK CHILDREN (CA) 2014-06-10 — — US disclosed
EP-2598150-A2 COMPOSITIONS FOR PROLIFERATION OF CELLS AND RELATED METHODS The Hospital For Sick Children (CA) 2013-06-05 — — EP disclosed
WO-2012018643-A2 COMPOSITIONS FOR PROLIFERATION OF CELLS AND RELATED METHODS THE HOSPITAL FOR SICK CHILDREN (CA) 2012-02-09 — — WO disclosed
US-20110301105-A1 COMPOSITIONS FOR PROLIFERATION OF CELLS AND RELATED METHODS THE HOSPITAL FOR SICK CHILDREN (CA) 2011-12-08 — — US disclosed
WO-2010039679-A1 COMPOSITIONS FOR PROLIFERATION OF CELLS AND RELATED METHODS THE HOSPITAL FOR SICK CHILDREN (CA) 2010-04-08 — — WO disclosed
CN-1178699-C Pharmaceutical Compsns. contg. compounds with activity for enhancement of absorption of active ingredients — 2004-12-08 — — CN disclosed
CN-1294519-A Pharmaceutical composition containing a compound having an activity of promoting the absorption of an active ingredient INPHARMA SA (CH) 2001-05-09 — — CN disclosed
EP-0179496-A1 16-Sulfinylmethyl-steroids, their preparation and use THE UPJOHN COMPANY (US) 1986-04-30 — — EP disclosed
US-4443377-A Isomerization-acylation process THE UPJOHN COMPANY (US) 1984-04-17 — — US disclosed
EP-0104054-A2 16-methylene-steroids and their preparation THE UPJOHN COMPANY (US) 1984-03-28 — — EP disclosed
EP-0034115-B1 PROCESS FOR THE PREPARATION OF 6-METHYLENE STEROIDS SCHERING AKTIENGESELLSCHAFT (DE) 1983-06-08 — — EP disclosed
US-4322349-A Process for preparing 6-methylene steroids SCHERING AKTIENGESELLSCHAFT (DE) 1982-03-30 — — US disclosed
EP-0034115-A2 Process for the preparation of 6-methylene steroids SCHERING AKTIENGESELLSCHAFT (DE) 1981-08-19 — — 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-20140234271-A1 COMPOSITIONS FOR PROLIFERATION OF CELLS AND RELATED METHODS MKI67, KRT18, PROX1 LMNA 2509/4885SHBG 1806/4885NR3C1 3193/4885
US-20110301105-A1 COMPOSITIONS FOR PROLIFERATION OF CELLS AND RELATED METHODS MKI67, KRT18, PROX1 LMNA 2509/4885SHBG 1806/4885NR3C1 3193/4885

“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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