SCHEMBL211665

SCHEMBL211665

CCC(c1ccc(O)cc1)C(CC)c1ccc(OC(C)=O)cc1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 6/20 0.63
LMNA P02545 3/20 0.63
CYP3A4 P08684 3/20 0.63
MAPT P10636 2/20 0.63
CYP2C9 P11712 2/20 0.63
ADRA1A P35348 2/20 0.63
SLC6A3 Q01959 2/20 0.63
CYP1A2 P05177 1/20 0.63
PGR P06401 1/20 0.63
CHRM2 P08172 1/20 0.63
ADORA3 P0DMS8 1/20 0.63
AR P10275 1/20 0.63
CYP2D6 P10635 1/20 0.63
CHRM1 P11229 1/20 0.63
ALOX15 P16050 1/20 0.63
DRD1 P21728 1/20 0.63
TBXA2R P21731 1/20 0.63
PTGS1 P23219 1/20 0.63
SLC6A2 P23975 1/20 0.63
CYP2C19 P33261 1/20 0.63

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
SCHEMBL211664 1.00 ESR1 (0.63) ESR1LMNACYP3A4MAPTCYP2C9
SCHEMBL2246272 0.93 ESR1 (0.71) ESR1LMNACYP3A4MAPTCYP2C9
SCHEMBL31356495 0.93 ESR1 (0.71) ESR1LMNACYP3A4MAPTCYP2C9
SCHEMBL21612683 0.91 ESR1 (0.69) ESR1LMNACYP3A4MAPTCYP2C9
SCHEMBL12521562 0.87 LMNA (0.47) ESR1LMNACYP3A4MAPTCYP2C9
SCHEMBL1107365 0.85 ESR1 (0.60) ESR1LMNACYP3A4MAPTCYP2C9
SCHEMBL22031202 0.82 LMNA (0.53) ESR1LMNACYP3A4MAPTCYP2C9
SCHEMBL22035223 0.82 LMNA (0.55) ESR1LMNACYP3A4MAPTCYP2C9
Hexestrol SCHEMBL27352072 0.82 ESR1 (0.79) ESR1LMNACYP3A4MAPTCYP2C9
4-Acetoxyphenol SCHEMBL203149 0.82 LMNA (0.67) ESR1LMNACYP3A4MAPTSLC6A3

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 87 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1754712-A2 Transcobalamin binding conjugates useful for treating abnormal cellular proliferation MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2007-02-21 EP claimed
US-20060166862-A1 Transcobalamin receptor binding conjugates useful for treating abnormal cellular proliferation REGENTS OF THE UNIVERSITY OF MINNESOTA 2006-07-27 US claimed
EP-1334114-A2 TRANSCOBALAMIN BINDING CONJUGATES USEFUL FOR TREATING ABNORMAL CELLULAR PROLIFERATION MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2003-08-13 EP claimed
US-20020151525-A1 Transcobalamin receptor binding conjugates useful for treating abnormal cellular proliferation COLLINS DOUGLAS A (US) 2002-10-17 US claimed
WO-2002055530-A2 TRANSCOBALAMIN BINDING CONJUGATES USEFUL FOR TREATING ABNORMAL CELLULAR PROLIFERATION MAYO FOUNDATION (US) 2002-07-18 WO claimed
US-20210015752-A1 METHODS FOR PRODUCING PARTICLES OF AN ACTIVE INGREDIENT SAVIOR LIFETEC CORPORATION (TW) 2021-01-21 US disclosed
CN-111093632-A Method for producing active ingredient particles 展旺生命科技股份有限公司 2020-05-01 CN disclosed
EP-3638212-A2 METHODS FOR PRODUCING PARTICLES OF AN ACTIVE INGREDIENT Savior Lifetec Corporation (TW) 2020-04-22 EP disclosed
WO-2018232053-A2 METHODS FOR PRODUCING PARTICLES OF AN ACTIVE INGREDIENT SAVIOR LIFETEC CORPORATION (TW) 2018-12-20 WO disclosed
WO-2018136909-A1 PREPARATION OF MICROPARTICLES OF AN ACTIVE INGREDIENT SAVIOR LIFETEC CORPORATION (TW) 2018-07-26 WO disclosed
EP-1765295-B1 SUSTAINED-RELEASE COMPOSITION, PROCESS FOR PRODUCING THE SAME AND USE OF THE SAME TAKEDA PHARMACEUTICAL (JP) 2012-09-12 EP disclosed
US-8088726-B2 Mixing an aqueous solution of a drug (LH-RH derivative) and an acid or base in a molar amount of about 1.5 or more times that of the drug with a solution of a biodegradable polymer, and drying the mixture; stable water in oil emulsion; reduced drug leakage during production; high drug content TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2012-01-03 US disclosed
US-5100669-A Controlled release drug delivery BIOMATERIALS UNIVERSE, INC. (JP) 1992-03-31 US disclosed
US-5061492-A biodegeadeable polymer matrix is copolymer of gylcolic acid a nd lactic acid TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1991-10-29 US disclosed
US-4917893-A Prolonged release microcapsules TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1990-04-17 US disclosed
EP-0330180-A1 Polylactic acid type microspheres containing physiologically active substance and process for preparing the same Biomaterials Universe, Inc. (JP) 1989-08-30 EP disclosed
EP-0145240-B1 METHOD FOR PRODUCING MICROCAPSULE Takeda Chemical Industries, Ltd. (JP) 1989-04-19 EP disclosed
US-4711782-A Prolonged release microcapsules and their production TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1987-12-08 US disclosed
US-4652441-A WATER SOLUBLE DRUGS TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1987-03-24 US disclosed
EP-0145240-A2 Method for producing Microcapsule Takeda Chemical Industries, Ltd. (JP) 1985-06-19 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-20060166862-A1 Transcobalamin receptor binding conjugates useful for treating abnormal cellular proliferation PCNA, MKI67, SLC19A1 ESR1 3737/4885LMNA 262/4885CYP3A4 3356/4885
US-20020151525-A1 Transcobalamin receptor binding conjugates useful for treating abnormal cellular proliferation PCNA, MKI67, SLC19A1 ESR1 3737/4885LMNA 262/4885CYP3A4 3356/4885

“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.