6-O-Benzylguanine

6-O-Benzylguanine

SCHEMBL600698

Nc1nc(OCc2ccccc2)c2nc[nH]c2n1

nearest known ligand 0.63

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MGMT P16455 6/20 0.63
PIN1 Q13526 6/20 0.63
CDK1 P06493 3/20 0.63
CCNB1 P14635 3/20 0.63
CCNA2 P20248 3/20 0.63
CDK2 P24941 3/20 0.63
CCNA1 P78396 3/20 0.63
CYP3A4 P08684 2/20 0.63
LMNA P02545 1/20 0.63
CYP1A2 P05177 1/20 0.63
CYP2D6 P10635 1/20 0.63
CYP2C9 P11712 1/20 0.63
TSHR P16473 1/20 0.63
NFKB1 P19838 1/20 0.63
CYP2C19 P33261 1/20 0.63
BLM P54132 1/20 0.63
PMP22 Q01453 1/20 0.63
MPO P05164 6/20 0.59
TPO P07202 1/20 0.59
EPX P11678 1/20 0.59

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
6-O-Benzylguanine SCHEMBL29405347 1.00 MGMT (0.63) MGMTPIN1CDK1CCNB1CCNA2
6-O-Benzylguanine SCHEMBL4631743 0.99 MGMT (0.61) MGMTPIN1CDK1CCNB1CCNA2
6-O-Benzylguanine SCHEMBL4869637 0.94 MGMT (0.56) MGMTPIN1CDK1CCNB1CCNA2
SCHEMBL3720508 0.87 MGMT (0.52) MGMTPIN1CDK1CCNB1CCNA2
6-O-Benzylguanine SCHEMBL10916356 0.87 PIN1 (0.50) MGMTPIN1CDK1CCNB1CCNA2
SCHEMBL21036999 0.86 PIN1 (0.51) MGMTPIN1CDK1CCNB1CCNA2
SCHEMBL15372394 0.86 PIN1 (0.64) MGMTPIN1CDK1CCNB1CCNA2
SCHEMBL1533391 0.86 MPO (0.61) MGMTPIN1CDK1CCNB1CCNA2
SCHEMBL13064122 0.85 MGMT (0.67) MGMTPIN1CDK1CCNB1CCNA2
SCHEMBL27090535 0.85 PIN1 (0.47) MGMTPIN1CDK1CCNB1CCNA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118852236-A Entecavir a synthetic intermediate of (C) preparation method of entecavir 南京工业大学 2024-10-29 CN claimed
CN-108371662-A A kind of application of five-ring heterocycles miazines compound 中国药科大学 2018-08-07 CN claimed
CN-101781301-B Method for preparing entecavir UNIV FUDAN 2013-04-10 CN claimed
EP-1644384-B1 PROCESS AND INTERMEDIATES FOR THE SYNTHESIS OF ENTECAVIR BRISTOL MYERS SQUIBB CO (US) 2012-10-31 EP claimed
JP-4726491-B2 2011-07-20 JP claimed
EP-1492791-B1 CRYSTAL AND SOLVATE OF 2-AMINO-6-BENZYLOXYPURINE AND PRODUCTION METHODS THEREOF SUMITOMO CHEMICAL CO (JP) 2008-06-04 EP claimed
US-7345170-B2 Crystal and solvate of 2-amino-6-benzyloxypurine and production methods thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2008-03-18 US claimed
US-20060106216-A1 Process for preparing the antiviral agent [1S-(1alpha, 3alpha, 4beta)]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one PENDRI YADAGIRI R 2006-05-18 US claimed
US-20060106215-A1 Process for preparing the antiviral agent [1S-(1alpha, 3alpha, 4beta)]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one CHAN YEUNG Y 2006-05-18 US claimed
US-7034152-B2 Process for preparing the antiviral agent [1S-(1alpha,3 alpha,4beta )]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one BRISTOL-MYERS SQUIBB COMPANY (US) 2006-04-25 US claimed
EP-1644384-A2 PROCESS AND INTERMEDIATES FOR SYNTHESIS ENTECAVIR Bristol-Myers Squibb Company (US) 2006-04-12 EP claimed
JP-2006509800-A 2006-03-23 JP claimed
US-20050080098-A1 Crystal and solvate of 2-amino-6-benzyloxypurine and production methods thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2005-04-14 US claimed
EP-1492791-A1 CRYSTAL AND SOLVATE OF 2-AMINO-6-BENZYLOXYPURINE AND PRODUCTION METHODS THEREOF Sumitomo Chemical Company, Limited (JP) 2005-01-05 EP claimed
US-20040192912-A1 Process for preparing the antiviral agent [1S-(1alpha,3 alpha,4beta)]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one BRISTOL-MYERS SQUIBB COMPANY 2004-09-30 US claimed
WO-2004052310-A2 PROCESS AND INTERMEDIATES FOR SYNTHESIS ENTECAVIR BRISTOL-MYERS SQUIBB COMPANY (US) 2004-06-24 WO claimed
WO-2003084957-A1 CRYSTAL AND SOLVATE OF 2-AMINO-6-BENZYLOXYPURINE AND PRODUCTION METHODS THEREOF SUMIKA FINE CHEMICALS CO., LTD. (JP) 2003-10-16 WO claimed
US-5064961-A PROCESS FOR PREPARING AN OPTICALLY ACTIVE CYCLOBUTANE NUCLEOSIDE E. R. SQUIBB & SONS, INC. (US) 1991-11-12 US claimed
US-4801710-A Regioselective synthesis of 9-substituted purine acyclonucleoside derivatives MERCK & CO., INC. (US) 1989-01-31 US claimed
EP-0184473-A1 Regioselective synthesis of 9-substituted purine acyclonucleoside derivatives MERCK & CO. INC. (US) 1986-06-11 EP claimed

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-20040192912-A1 Process for preparing the antiviral agent [1S-(1alpha,3 alpha,4beta)]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one SAMHD1, NUDT1, ENTPD1 MGMT 1661/4885PIN1 4218/4885CDK1 1762/4885
US-20060106216-A1 Process for preparing the antiviral agent [1S-(1alpha, 3alpha, 4beta)]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one SAMHD1, NUDT1, ENTPD1 MGMT 1680/4885PIN1 4133/4885CDK1 1666/4885
US-20060106215-A1 Process for preparing the antiviral agent [1S-(1alpha, 3alpha, 4beta)]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one SAMHD1, NUDT1, ENTPD1 MGMT 1680/4885PIN1 4133/4885CDK1 1666/4885

“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.