SCHEMBL5872206

SCHEMBL5872206

[CH2]c1cc(C)cc(CCl)c1O

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AMY1A P0DUB6 1/20 0.37
HSPA5 P11021 1/20 0.37
CYP2C9 P11712 2/20 0.36
CYP2C19 P33261 2/20 0.36
HIF1A Q16665 2/20 0.36
SMN1; SMN2 Q16637 2/20 0.36
SELL P14151 1/20 0.36
SELP P16109 1/20 0.36
SELE P16581 1/20 0.36
ACHE P22303 1/20 0.36
CYP2D6 P10635 1/20 0.33
HSD17B10 Q99714 1/20 0.33
ALDH1A1 P00352 3/20 0.32
KDM4E B2RXH2 2/20 0.32
KMT2A Q03164 2/20 0.32
PON1 P27169 1/20 0.32
MAPK1 P28482 1/20 0.32
RAB9A P51151 1/20 0.32
AURKA O14965 1/20 0.32
AURKB Q96GD4 1/20 0.32

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
SCHEMBL4408009 0.84 AMY1A (0.48) AMY1AHSPA5CYP2C9CYP2C19HIF1A
SCHEMBL544678 0.78 KDM4E (0.46) AMY1AHSPA5CYP2C9CYP2C19HIF1A
SCHEMBL30558173 0.78 KDM4E (0.46) AMY1AHSPA5CYP2C9CYP2C19HIF1A
SCHEMBL2809409 0.77 ACHE (0.50) AMY1AHSPA5CYP2C9CYP2C19HIF1A
SCHEMBL11836795 0.74 KMT2A (0.38) AMY1AHSPA5CYP2C9CYP2C19HIF1A
SCHEMBL29072242 0.72 HSPA5 (0.72) HSPA5CYP2C9CYP2C19HIF1ASMN1; SMN2
SCHEMBL14999517 0.71 ERN1 (0.64) AMY1AHSPA5SMN1; SMN2ALDH1A1KDM4E
SCHEMBL29072282 0.71 TYR (0.42) AMY1AHSPA5CYP2C9CYP2C19HIF1A
SCHEMBL30809972 0.71 ERN1 (0.64) AMY1AHSPA5SMN1; SMN2ALDH1A1KDM4E
SCHEMBL3641181 0.70 ALDH1A1 (0.52) CYP2C9CYP2C19SMN1; SMN2SELLSELP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20060270855-A1 Methods of preparing retroviral proteases inhibitor intermediates G.D. SEARLE & CO. (US) 2006-11-30 US disclosed
US-7060851-B2 Method of preparing retroviral protease inhibitor intermediates G.D. SEARLE & CO. (US) 2006-06-13 US disclosed
US-20050131075-A1 Method of preparing retroviral protease inhibitor intermediates G.D. SEARLE & CO. (US) 2005-06-16 US disclosed
CN-1623977-A Method of preparing retroviral protease inhibitor intermediates SEARLE & CO (US) 2005-06-08 CN disclosed
US-6849760-B2 Method of preparing retroviral protease inhibitor intermediates G. D. SEARLE & CO. (US) 2005-02-01 US disclosed
US-20030171612-A1 Method of preparing retroviral protease inhibitor intermediates G.D. SEARLE & CO. 2003-09-11 US disclosed
US-6515162-B2 Precipitating or crystallizing a salt from solution; suitable as intermediates for large scale production of enzyme inhibitors, e.g. hydroxyethylamine, hydroxyethylurea and hydroxyethylsulfonamide G.D. SEARLE & CO. 2003-02-04 US disclosed
US-20010047111-A1 Method of preparing retroviral protease inhibitor intermediates NG JOHN S (US) 2001-11-29 US disclosed
EP-0804410-B1 METHOD OF PREPARING RETROVIRAL PROTEASE INHIBITOR INTERMEDIATES SEARLE & CO (US) 2001-08-29 EP disclosed
US-6201150-B1 DIASTEREOMER PURIFICATION METHOD COMPRISING PREPARING AN ORGANIC ACID OR INORGANIC ACID SALT OF AN AMINO COMPOUND AND PRECIPITATING OR CRYSTALLIZING SAID SALT FROM A SOLUTION G.D. SEARLE & CO. 2001-03-13 US disclosed
US-5831117-A ACID SALTS G. D. SEARLE & CO. (US) 1998-11-03 US disclosed
CN-1177955-A Process for preparing retroviral protease inhibitor intermediates SEARLE & CO (US) 1998-04-01 CN disclosed
EP-0804410-A1 METHOD OF PREPARING RETROVIRAL PROTEASE INHIBITOR INTERMEDIATES G.D. SEARLE & CO. (US) 1997-11-05 EP disclosed
WO-1996022275-A1 METHOD OF PREPARING RETROVIRAL PROTEASE INHIBITOR INTERMEDIATES G.D. SEARLE & CO. (US) 1996-07-25 WO 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 (4 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-20060270855-A1 Methods of preparing retroviral proteases inhibitor intermediates ACE, REN, MME AMY1A 1804/4885HSPA5 3556/4885CYP2C9 2418/4885
US-20030171612-A1 Method of preparing retroviral protease inhibitor intermediates ACE, REN, MME AMY1A 1813/4885HSPA5 3749/4885CYP2C9 2154/4885
US-20010047111-A1 Method of preparing retroviral protease inhibitor intermediates ACE, REN, MME AMY1A 1813/4885HSPA5 3749/4885CYP2C9 2154/4885
US-20050131075-A1 Method of preparing retroviral protease inhibitor intermediates ACE, REN, MME AMY1A 1744/4885HSPA5 3768/4885CYP2C9 1951/4885

“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.