SCHEMBL2301281

SCHEMBL2301281

O=Cc1ccc(N=Nc2ccccc2)cc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 4/20 0.59
▸ CYP2A6 P11509 2/20 0.59
▸ MAPT P10636 5/20 0.50
▸ MEN1 O00255 4/20 0.50
▸ KMT2A Q03164 4/20 0.50
▸ RAB9A P51151 3/20 0.50
▸ NPC1 O15118 2/20 0.50
▸ PKM P14618 1/20 0.50
▸ HTT P42858 1/20 0.50
▸ TRPA1 O75762 1/20 0.50
▸ MAPK1 P28482 2/20 0.47
▸ TDP1 Q9NUW8 2/20 0.47
▸ KDM4E B2RXH2 1/20 0.47
▸ HSP90AA1 P07900 1/20 0.47
▸ POLB P06746 1/20 0.47
▸ CYP2D6 P10635 1/20 0.47
▸ HSD17B10 Q99714 2/20 0.45
▸ TSHR P16473 1/20 0.45
▸ SMN1; SMN2 Q16637 1/20 0.42
▸ CASP3 P42574 1/20 0.42

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
SCHEMBL7542217 1.00 ALDH1A1 (0.59) ALDH1A1CYP2A6MAPTMEN1KMT2A
SCHEMBL5469857 0.90 CYP2A6 (0.50) ALDH1A1CYP2A6MAPTMEN1KMT2A
SCHEMBL3074403 0.90 CYP2A6 (0.50) ALDH1A1CYP2A6MAPTMEN1KMT2A
SCHEMBL9640411 0.82 ALDH1A1 (0.52) ALDH1A1CYP2A6MAPTMEN1KMT2A
SCHEMBL9640413 0.82 ALDH1A1 (0.52) ALDH1A1CYP2A6MAPTMEN1KMT2A
SCHEMBL2316309 0.80 ALDH1A1 (0.52) ALDH1A1CYP2A6MAPTMEN1KMT2A
SCHEMBL15355549 0.80 ALDH1A1 (0.63) ALDH1A1MAPTMEN1KMT2ARAB9A
SCHEMBL13451257 0.80 ALDH1A1 (0.63) ALDH1A1MAPTMEN1KMT2ARAB9A
SCHEMBL15132514 0.79 ALDH5A1 (0.73) ALDH1A1MAPTMEN1KMT2ARAB9A
SCHEMBL28987870 0.79 PTGS1 (0.44) ALDH1A1CYP2A6MAPTMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115038790-B Synthesis of 3' -RNA oligonucleotides 阿尔尼拉姆医药品有限公司 2024-06-21 — — CN claimed
WO-2023064530-A1 EXTRA-HEPATIC DELIVERY IRNA COMPOSITIONS AND METHODS OF USE THEREOF ALNYLAM PHARMACEUTICALS, INC. (US) 2023-04-20 — — WO claimed
CN-115038790-A Synthesis of 3' -RNA oligonucleotides 阿尔尼拉姆医药品有限公司 2022-09-09 — — CN claimed
US-20110201528-A1 Methods Of Forming An Oligomer Array KUMHO PETROCHEMICAL CO., LTD. (KP) 2011-08-18 — — US claimed
US-7622248-B2 Ribozymes with broad tRNA aminoacylation activity THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 2009-11-24 — — US claimed
US-7271258-B2 Methods of synthesizing oligonucleotides using carbonate protecting groups and alpha-effect nucleophile deprotection AGILENT TECHNOLOGIES, INC. (US) 2007-09-18 — — US claimed
US-20060252924-A1 Methods of synthesizing oligonucleotides using carbonate protecting groups and alpha-effect nucleophile deprotection THE REGENTS OF THE UNIVERSITY OF COLORADO 2006-11-09 — — US claimed
EP-1483282-A1 RIBOZYMES WITH BROAD tRNA AMINOACYLATION ACTIVITY The Research Foundation of State University of New York (US) 2004-12-08 — — EP claimed
US-20030228593-A1 Ribozymes with broad tRNA aminoacylation activity RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK, THE 2003-12-11 — — US claimed
US-6630581-B2 Condensing the 3'-OH or 5'-OH group of a support-bound nucleoside or oligonucleotide with a monomeric nucleoside phosphoramidite having a carbonate-protected hydroxyl group; treating the intermediate provided with a deprotecting reagent AGILENT TECHNOLOGIES, INC. 2003-10-07 — — US claimed
WO-2003070740-A1 RIBOZYMES WITH BROAD tRNA AMINOACYLATION ACTIVITY THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 2003-08-28 — — WO claimed
US-20020045221-A1 Solid phase synthesis of oligonucleotides using carbonate protecting groups and alpha-effect nucleophile deprotection THE REGENTS OF THE UNIVERSITY OF COLORADO 2002-04-18 — — US claimed
US-6222030-B1 CONDENSING HYDROXY GROUP OF BOUND OLIGONUCLEOTIDE OR NUCLEOSIDE WITH NUCLEOSIDE PHOSPHORAMIDITE HAVING CARBONATE-PROTECTED HYDROXYL GROUP, TREATING WITH DEPROTECTING AGENT ALSO OXIDIZES PHOSPHITE TRIESTER LINKAGE AGILENT TECHNOLOGIES, INC. 2001-04-24 — — US claimed
US-4176009-A HYDROLYZING OLIGOPEPTIDES IN A AQUEOUS SOLUTION TO RELEASE PEPTIDE FRAGMENTS, USING COLORIMETRIC ANALYSIS AFTER SOLVENT EXTRACTION AJINOMOTO CO., INC. (JP) 1979-11-27 — — US claimed
US-4138394-A Peptide derivatives and a method of measuring collagenase activity AJINOMOTO CO., INC. (JP) 1979-02-06 — — US claimed
JP-53028165-A — — None — — JP disclosed
CN-115038790-B Synthesis of 3' -RNA oligonucleotides 阿尔尼拉姆医药品有限公司 2024-06-21 — — CN disclosed
US-3956269-A POLYMERIZATION CATALYSTS PENNWALT CORPORATION (US) 1976-05-11 — — US disclosed
US-3954475-A Photosensitive elements containing chromophore-substituted vinyl-halomethyl-s-triazines MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1976-05-04 — — US disclosed
JP-S05328165-A — — 0001-01-01 — — JP 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 (2 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-20060252924-A1 Methods of synthesizing oligonucleotides using carbonate protecting groups and alpha-effect nucleophile deprotection POLL, DNTT, RNGTT ALDH1A1 2559/4885CYP2A6 3959/4885MAPT 3581/4885
US-20020045221-A1 Solid phase synthesis of oligonucleotides using carbonate protecting groups and alpha-effect nucleophile deprotection POLL, RNGTT, DNTT ALDH1A1 2882/4885CYP2A6 3487/4885MAPT 3855/4885

“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.

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