SCHEMBL986291

SCHEMBL986291

COC(=O)C1CCC(C)(C(=O)O)C1(C)C

nearest known ligand 0.60

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 2/20 0.60
CYP2C9 P11712 1/20 0.60
TSHR P16473 1/20 0.60
CYP2C19 P33261 1/20 0.60
ALDH1A1 P00352 3/20 0.58
LMNA P02545 2/20 0.55
POLB P06746 1/20 0.55
NPSR1 Q6W5P4 4/20 0.50
L3MBTL1 Q9Y468 3/20 0.50
ATM Q13315 2/20 0.48
MEN1 O00255 1/20 0.47
KMT2A Q03164 1/20 0.47
HTT P42858 1/20 0.46
TP53 P04637 1/20 0.46
HIF1A Q16665 1/20 0.34
PPM1B O75688 1/20 0.33
PTPN1 P18031 1/20 0.33
PTGS2 P35354 1/20 0.33

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
SCHEMBL2533909 1.00 CYP1A2 (0.60) CYP1A2CYP2C9TSHRCYP2C19ALDH1A1
SCHEMBL2534532 1.00 CYP1A2 (0.60) CYP1A2CYP2C9TSHRCYP2C19ALDH1A1
SCHEMBL7227981 1.00 CYP1A2 (0.60) CYP1A2CYP2C9TSHRCYP2C19ALDH1A1
SCHEMBL7220705 1.00 CYP1A2 (0.60) CYP1A2CYP2C9TSHRCYP2C19ALDH1A1
SCHEMBL2535775 0.88 CYP1A2 (0.50) CYP1A2CYP2C9TSHRCYP2C19ALDH1A1
SCHEMBL2534983 0.88 CYP1A2 (0.50) CYP1A2CYP2C9TSHRCYP2C19ALDH1A1
SCHEMBL2534980 0.88 CYP1A2 (0.50) CYP1A2CYP2C9TSHRCYP2C19ALDH1A1
SCHEMBL1335665 0.85 ALDH1A1 (0.54) CYP1A2CYP2C9TSHRCYP2C19ALDH1A1
SCHEMBL16386442 0.85 CYP1A2 (0.56) CYP1A2CYP2C9TSHRCYP2C19ALDH1A1
SCHEMBL12699010 0.85 CYP1A2 (0.56) CYP1A2CYP2C9TSHRCYP2C19ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3930724-B1 METHOD AND COMPOSITION FOR INHIBITING VIRUS INFECTION ARJIL BIOTECH HOLDING COMPANY LTD (TW) 2024-07-03 EP disclosed
US-20240148753-A1 METHOD AND COMPOSITION FOR REVERSING AND/OR INHIBITING ATHEROSCLEROSIS Arjil Biotech Holding Company Limited (TW) 2024-05-09 US disclosed
CN-113795258-B Methods and compositions for inhibiting viral infection 吉亚生技控股股份有限公司 2024-04-16 CN disclosed
EP-3955947-A1 METHOD AND COMPOSITION FOR REVERSING AND/OR INHIBITING ATHEROSCLEROSIS Arjil Biotech Holding Company Limited (TW) 2022-02-23 EP disclosed
US-11253527-B2 Method and composition for inhibiting virus infection Arjil Biotech Holding Company Limited (TW) 2022-02-22 US disclosed
EP-3930724-A1 METHOD AND COMPOSITION FOR INHIBITING VIRUS INFECTION Arjil Biotech Holding Company Limited (TW) 2022-01-05 EP disclosed
WO-2020214919-A1 METHOD AND COMPOSITION FOR REVERSING AND/OR INHIBITING ATHEROSCLEROSIS Arjil Biotech Holding Company Limited (TW) 2020-10-22 WO disclosed
US-20200330485-A1 METHOD AND COMPOSITION FOR REVERSING AND/OR INHIBITING ATHEROSCLEROSIS Arjil Biotech Holding Company Limited (TW) 2020-10-22 US disclosed
US-20200268771-A1 METHOD AND COMPOSITION FOR INHIBITING VIRUS INFECTION Arjil Biotech Holding Company Limited (TW) 2020-08-27 US disclosed
EP-3415145-A2 METHOD FOR TREATING STROKE OR REDUCING NERVE INJURY Arjil Biotech Holding Company Limited (TW) 2018-12-19 EP disclosed
US-20110257164-A1 DIPEPTIDYL PEPTIDASE IV INHIBITORS ORCHID RESEARCH LABORATORIES LIMITED (IN) 2011-10-20 US disclosed
EP-2344463-A2 1,2 -THIAZOL YL DERIVATIVES AS CANNABINOID RECEPTOR LIGANDS Abbott Laboratories (US) 2011-07-20 EP disclosed
US-20110082116-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 2011-04-07 US disclosed
US-7872033-B2 N-[(5Z)-4-butyl-2-tert-butylisothiazol-5(2H)-ylidene]-5-chloro-2-methoxybenzamide; CB2 receptors ligand; antiinflammatory, analgesic agent; autoimmune diseases; neuroprotectants ABBOTT LABORATORIES (US) 2011-01-18 US disclosed
US-20100234345-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 2010-09-16 US disclosed
WO-2010079413-A2 DIPEPTIDYL PEPTIDASE IV INHIBITORS ORCHID RESEARCH LABORATORIES LTD. (IN) 2010-07-15 WO disclosed
WO-2010054024-A2 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 2010-05-14 WO disclosed
EP-2146973-A2 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS Abbott Laboratories (US) 2010-01-27 EP disclosed
US-20090023789-A1 N-[(5Z)-4-butyl-2-tert-butylisothiazol-5(2H)-ylidene]-5-chloro-2-methoxybenzamide; CB2 receptors ligand; antiinflammatory, analgesic agent; autoimmune diseases; neuroprotectants ABBOTT LABORATORIES (US) 2009-01-22 US disclosed
WO-2008130953-A2 2-IMIN0IS0THIAZ0LE DERIVATIVES AS CANNABINOID RECEPTOR LIGANDS ABBOTT LABORATORIES (US) 2008-10-30 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 (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-20200268771-A1 METHOD AND COMPOSITION FOR INHIBITING VIRUS INFECTION HAVCR2, HDGF, ZC3HAV1 CYP1A2 2185/4885CYP2C9 3048/4885TSHR 4854/4885
US-20090023789-A1 N-[(5Z)-4-butyl-2-tert-butylisothiazol-5(2H)-ylidene]-5-chloro-2-methoxybenzamide; CB2 receptors ligand; antiinflammatory, analgesic agent; autoimmune diseases; neuroprotectants CNR2, CNR1, TBXA2R CYP1A2 1304/4885CYP2C9 1950/4885TSHR 192/4885
US-11253527-B2 Method and composition for inhibiting virus infection HAVCR2, HDGF, ZC3HAV1 CYP1A2 2185/4885CYP2C9 3048/4885TSHR 4854/4885
US-20200330485-A1 METHOD AND COMPOSITION FOR REVERSING AND/OR INHIBITING ATHEROSCLEROSIS HMGCR, CYP46A1, PCSK9 CYP1A2 1864/4885CYP2C9 2545/4885TSHR 4402/4885
US-20110082116-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS CNR1, CNR2, GPR18 CYP1A2 1251/4885CYP2C9 1580/4885TSHR 292/4885
US-20110257164-A1 DIPEPTIDYL PEPTIDASE IV INHIBITORS DPP4, DPP7, DPP3 CYP1A2 429/4885CYP2C9 186/4885TSHR 1137/4885
US-20100234345-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS CNR1, CNR2, GPR18 CYP1A2 1266/4885CYP2C9 1462/4885TSHR 285/4885
US-20240148753-A1 METHOD AND COMPOSITION FOR REVERSING AND/OR INHIBITING ATHEROSCLEROSIS PCSK9, APOB, PCSK7 CYP1A2 2468/4885CYP2C9 2727/4885TSHR 4662/4885

“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.