SCHEMBL845072

SCHEMBL845072

CCC(C(=O)c1ccc(OCCCl)cc1)c1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 9/20 0.61
HSD17B10 Q99714 1/20 0.61
SMN1; SMN2 Q16637 9/20 0.56
MAPT P10636 4/20 0.56
MITF O75030 3/20 0.56
RAB9A P51151 2/20 0.56
NLRP1 Q9C000 1/20 0.56
TP53 P04637 2/20 0.54
JAK2 O60674 2/20 0.54
MEN1 O00255 1/20 0.54
THRB P10828 1/20 0.54
KMT2A Q03164 1/20 0.54
PAX8 Q06710 1/20 0.49
ALDH1A1 P00352 3/20 0.49
TSHR P16473 2/20 0.46
HPGD P15428 1/20 0.46
HIF1A Q16665 1/20 0.46
PKM P14618 1/20 0.45
GAA P10253 2/20 0.45
PARP10 Q53GL7 1/20 0.43

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
SCHEMBL8766911 0.95 LMNA (0.61) LMNAHSD17B10SMN1; SMN2MAPTMITF
SCHEMBL8767682 0.93 LMNA (0.59) LMNAHSD17B10SMN1; SMN2MAPTMITF
SCHEMBL10828017 0.92 LMNA (0.58) LMNAHSD17B10SMN1; SMN2MAPTMITF
SCHEMBL8766893 0.92 LMNA (0.58) LMNAHSD17B10SMN1; SMN2MAPTMITF
SCHEMBL8645421 0.92 LMNA (0.58) LMNAHSD17B10SMN1; SMN2MAPTMITF
SCHEMBL22773415 0.88 LMNA (0.46) LMNAHSD17B10SMN1; SMN2MAPTMITF
SCHEMBL11500794 0.88 LMNA (0.62) LMNAHSD17B10SMN1; SMN2MAPTMITF
SCHEMBL19659872 0.87 LMNA (0.45) LMNAHSD17B10SMN1; SMN2MAPTMITF
SCHEMBL13531143 0.86 LMNA (0.61) LMNAHSD17B10SMN1; SMN2MAPTMITF
SCHEMBL7991466 0.86 LMNA (0.61) LMNAHSD17B10SMN1; SMN2MAPTMITF

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240246904-A1 FUNCTIONALIZED N,N-DIALKYLAMINO PHENYL ETHERS AND THEIR METHOD OF USE UNIV TEMPLE (US) 2024-07-25 US disclosed
US-11873267-B2 Functionalized N,N-dialkylamino phenyl ethers and their method of use TEMPLE UNIVERSITY-OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2024-01-16 US disclosed
US-11873267-B2 Functionalized N,N-dialkylamino phenyl ethers and their method of use TEMPLE UNIVERSITY-OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2024-01-16 US disclosed
US-11873267-B2 Functionalized N,N-dialkylamino phenyl ethers and their method of use TEMPLE UNIVERSITY-OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2024-01-16 US disclosed
US-11672758-B2 Endoxifen methods and compositions for inhibition of protein kinase C JINA PHARMACEUTICALS, INC. (US) 2023-06-13 US disclosed
US-11672758-B2 Endoxifen methods and compositions for inhibition of protein kinase C JINA PHARMACEUTICALS, INC. (US) 2023-06-13 US disclosed
US-11672758-B2 Endoxifen methods and compositions for inhibition of protein kinase C JINA PHARMACEUTICALS, INC. (US) 2023-06-13 US disclosed
EP-3981766-A1 INDAZOLE DERIVATIVES USEFUL IN THE TREATMENT OF CANCER Eisai R&D Management Co., Ltd. (JP) 2022-04-13 EP disclosed
EP-3981766-A1 INDAZOLE DERIVATIVES USEFUL IN THE TREATMENT OF CANCER Eisai R&D Management Co., Ltd. (JP) 2022-04-13 EP disclosed
CN-113024466-A Tetra-substituted olefin compound and use thereof 卫材 R&D 管理有限公司 2021-06-25 CN disclosed
WO-2008070463-A2 ENDOXIFEN METHODS AND COMPOSITIONS JINA PHARMACEUTICALS, INC. (US) 2008-06-12 WO disclosed
WO-2007098090-A2 TREATMENT OF HYPERPROLIFERATIVE DISEASES WITH N-OXIDES OF ESTROGEN RECEPTOR MODULATORS NOVACEA, INC. (US) 2007-08-30 WO disclosed
WO-2004012723-A1 TAMOXIFEN CONTAINING NOT MORE THAN 0.006% E-ISOMER KYMED GB LTD. (GB) 2004-02-12 WO disclosed
US-6172263-B1 PURIFICATION; SOLVENT EXTRACTION WITH METHANOL; CRYSTALLIZATION BRADFORD UNIVERSITY (GB) 2001-01-09 US disclosed
EP-0998447-A1 TAMOXIFEN AND ANALOGUES THEREOF UNIVERSITY OF BRADFORD (GB) 2000-05-10 EP disclosed
US-5962743-A Process for preparing acylaromatic compounds CATALYTICA PHARMACEUTICALS, INC. (US) 1999-10-05 US disclosed
WO-1999005088-A1 TAMOXIFEN AND ANALOGUES THEREOF UNIVERSITY OF BRADFORD (GB) 1999-02-04 WO disclosed
EP-0260066-B1 TAMOXIFEN DERIVATIVES NATIONAL RESEARCH DEVELOPMENT CORPORATION (GB) 1990-05-09 EP disclosed
US-4839155-A Iodotamoxifen derivatives and use for estrogen receptor-positive breast cancer detection and therapy NATIONAL RESEARCH DEVELOPMENT CORPORATION (GB) 1989-06-13 US disclosed
EP-0260066-A1 Tamoxifen derivatives NATIONAL RESEARCH DEVELOPMENT CORPORATION (GB) 1988-03-16 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 (3 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-11873267-B2 Functionalized N,N-dialkylamino phenyl ethers and their method of use GAA, GBA1, GBA2 LMNA 95/4885HSD17B10 2878/4885SMN1; SMN2 114/4885
US-20240246904-A1 FUNCTIONALIZED N,N-DIALKYLAMINO PHENYL ETHERS AND THEIR METHOD OF USE GAA, GBA1, GBA2 LMNA 95/4885HSD17B10 2878/4885SMN1; SMN2 114/4885
US-11672758-B2 Endoxifen methods and compositions for inhibition of protein kinase C EEF2K, LITAF, RAPGEF3 LMNA 948/4885HSD17B10 3559/4885SMN1; SMN2 811/4885

“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.