SCHEMBL4740749

SCHEMBL4740749

COc1ccc(CCCCCO)cc1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CALM1 P0DP23 1/20 0.63
IGF1R P08069 1/20 0.61
ALOX15 P16050 1/20 0.61
CYP4F2 P78329 1/20 0.56
CYP4A11 Q02928 1/20 0.56
TDP1 Q9NUW8 1/20 0.54
L3MBTL1 Q9Y468 1/20 0.54
TAAR1 Q96RJ0 1/20 0.53
ALOX5 P09917 1/20 0.53
F2RL1 P55085 1/20 0.50
GAA P10253 1/20 0.49
MEN1 O00255 1/20 0.49
USP2 O75604 1/20 0.49
ALDH1A1 P00352 1/20 0.49
LMNA P02545 1/20 0.49
CYP3A4 P08684 1/20 0.49
MAPK1 P28482 1/20 0.49
CASP1 P29466 1/20 0.49
KMT2A Q03164 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.49

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
SCHEMBL8862032 1.00 CALM1 (0.63) CALM1IGF1RALOX15CYP4F2CYP4A11
SCHEMBL8413383 1.00 CALM1 (0.63) CALM1IGF1RALOX15CYP4F2CYP4A11
SCHEMBL1171813 0.98 CALM1 (0.66) CALM1IGF1RALOX15CYP4F2CYP4A11
SCHEMBL79113 0.92 CALM1 (0.68) CALM1IGF1RALOX15CYP4A11TAAR1
SCHEMBL10571532 0.89 CALM1 (0.69) CALM1IGF1RALOX15TDP1L3MBTL1
SCHEMBL17400406 0.89 CALM1 (0.69) CALM1IGF1RALOX15TDP1L3MBTL1
SCHEMBL9509173 0.89 CALM1 (0.69) CALM1IGF1RALOX15TDP1L3MBTL1
SCHEMBL11007798 0.89 CALM1 (0.69) CALM1IGF1RALOX15TDP1L3MBTL1
SCHEMBL28218193 0.89 CALM1 (0.69) CALM1IGF1RALOX15TDP1L3MBTL1
SCHEMBL4254058 0.87 CALM1 (0.72) CALM1IGF1RALOX15TDP1L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12398168-B2 Preparation method of a glycoside compound SHANGHAI HUTCHISON PHARMACEUTICALS LIMITED (CN) 2025-08-26 US disclosed
US-20220380399-A1 PREPARATION METHOD OF A GLYCOSIDE COMPOUND SHANGHAI HUTCHISON PHARMACEUTICALS LIMITED (CN) 2022-12-01 US disclosed
CN-113651729-B Preparation method of iron-catalyzed 4-aminoalcohol 西安交通大学 2022-10-28 CN disclosed
US-11325937-B2 Glycoside compound and preparation method therefor, composition, application, and intermediate SHANGHAI HUTCHISON PHARMACEUTICALS LIMITED (CN) 2022-05-10 US disclosed
CN-113651729-A Preparation method of iron-catalyzed 4-aminoalcohol 西安交通大学 2021-11-16 CN disclosed
WO-2021139621-A1 METHOD FOR PREPARING GLYCOSIDE COMPOUND 上海和黄药业有限公司 2021-07-15 WO disclosed
CN-112851456-A Method for preparing olefin compound under alkaline condition 扬州工业职业技术学院 2021-05-28 CN disclosed
EP-3819303-A1 GLYCOSIDE COMPOUND AND PREPARATION METHOD THEREFOR, COMPOSITION, APPLICATION, AND INTERMEDIATE Shanghai Hutchison Pharmaceuticals Limited (CN) 2021-05-12 EP disclosed
US-20210115082-A1 GLYCOSIDE COMPOUND AND PREPARATION METHOD THEREFOR, COMPOSITION, APPLICATION, AND INTERMEDIATE SHANGHAI HUTCHISON PHARMACEUTICALS LIMITED (CN) 2021-04-22 US disclosed
WO-2008081096-A2 QUINOLINYL DERIVATIVES, METHOD FOR PREPARING SAME, PHARMACEUTIC COMPOSITIONS CONTAINING SAME, AND USE THEREOF AS HYPOGLYCEMIANT AND HYPOLIPEMIANT AGENTS LES LABORATOIRES SERVIER (FR) 2008-07-10 WO disclosed
US-20040198746-A1 Sodium channel blockers PARION SCIENCES, INC. (US) 2004-10-07 US disclosed
US-20040198745-A1 Sodium channel blockers PARION SCIENCES, INC. (US) 2004-10-07 US disclosed
US-20040198747-A1 Sodium channel blockers PARION SCIENCES, INC. (US) 2004-10-07 US disclosed
US-20030195160-A1 Sodium channel blockers CYFI, INC. 2003-10-16 US disclosed
WO-2003070184-A2 SODIUM CHANNEL BLOCKERS JOHNSON MICHAEL R (US) 2003-08-28 WO disclosed
EP-1107944-A1 AMINOALCOHOL DERIVATIVES AND THEIR USE AS BETA 3 ADRENERGIC AGONISTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2001-06-20 EP disclosed
WO-2000012462-A1 AMINOALCOHOL DERIVATIVES AND THEIR USE AS BETA 3 ADRENERGIC AGONISTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2000-03-09 WO disclosed
EP-0162208-B1 NOVEL N-SUBSTITUTED 3,4-DIHYDROPYRIMIDINE DERIVATIVES, PROCESSES FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS SUNTORY KABUSHIKI KAISHA, also known as SUNTORY LTD. (JP) 1989-11-23 EP disclosed
US-4683234-A HYPOTENSIVE AGENTS, ANTI-ANGINA SUNTORY LIMITED (JP) 1987-07-28 US disclosed
EP-0162208-A2 Novel N-substituted 3,4-dihydropyrimidine derivatives, processes for preparing them and pharmaceutical compositions SUNTORY KABUSHIKI KAISHA, also known as SUNTORY LTD. (JP) 1985-11-27 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 (8 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-20030195160-A1 Sodium channel blockers HCN4, SCN2B, SCN5A CALM1 548/4885IGF1R 4865/4885ALOX15 2153/4885
US-20040198747-A1 Sodium channel blockers HCN4, SCN2B, SCN5A CALM1 548/4885IGF1R 4865/4885ALOX15 2153/4885
US-12398168-B2 Preparation method of a glycoside compound GALE, ST6GAL1, MGAM CALM1 4863/4885IGF1R 4200/4885ALOX15 3217/4885
US-20220380399-A1 PREPARATION METHOD OF A GLYCOSIDE COMPOUND GALE, ST6GAL1, MGAM CALM1 4863/4885IGF1R 4200/4885ALOX15 3217/4885
US-11325937-B2 Glycoside compound and preparation method therefor, composition, application, and intermediate VEGFA, FLT4, FLT1 CALM1 3278/4885IGF1R 86/4885ALOX15 1291/4885
US-20040198745-A1 Sodium channel blockers SCN2B, SCN4A, SCN1B CALM1 836/4885IGF1R 4370/4885ALOX15 3938/4885
US-20040198746-A1 Sodium channel blockers HCN4, SCN2B, SCN5A CALM1 548/4885IGF1R 4865/4885ALOX15 2153/4885
US-20210115082-A1 GLYCOSIDE COMPOUND AND PREPARATION METHOD THEREFOR, COMPOSITION, APPLICATION, AND INTERMEDIATE VEGFA, FLT4, FLT1 CALM1 3278/4885IGF1R 86/4885ALOX15 1291/4885

“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.