SCHEMBL2008561

SCHEMBL2008561

CON[C@@H](C)C(=O)OP(=O)(Cl)Oc1ccc(Br)cc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.41
ALDH1A1 P00352 5/20 0.39
KDM4E B2RXH2 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
KMT2A Q03164 3/20 0.38
MEN1 O00255 2/20 0.38
NPSR1 Q6W5P4 2/20 0.38
MAPT P10636 1/20 0.38
MAPK1 P28482 1/20 0.38
RAB9A P51151 1/20 0.38
RXFP1 Q9HBX9 1/20 0.38
POLB P06746 1/20 0.34
CA2 P00918 1/20 0.33
MMP2 P08253 1/20 0.33
MMP9 P14780 1/20 0.33
MMP8 P22894 1/20 0.33
MMP14 P50281 1/20 0.33
CA9 Q16790 1/20 0.33
CA14 Q9ULX7 1/20 0.33
GAA P10253 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
SCHEMBL2008560 1.00 LMNA (0.41) LMNAALDH1A1KDM4ESMN1; SMN2KMT2A
SCHEMBL10004082 0.91 CA1 (0.38) SMN1; SMN2KMT2AMEN1RAB9ACA2
SCHEMBL1811991 0.88 HPGD (0.39) LMNAALDH1A1KMT2AMEN1NPSR1
SCHEMBL2008909 0.87 LMNA (0.39) LMNAALDH1A1KDM4ESMN1; SMN2KMT2A
SCHEMBL2008911 0.87 LMNA (0.39) LMNAALDH1A1KDM4ESMN1; SMN2KMT2A
SCHEMBL1807789 0.87 CYP1A2 (0.37) LMNAALDH1A1KDM4ESMN1; SMN2KMT2A
SCHEMBL7023448 0.87 APP (0.32) ALDH1A1SMN1; SMN2RAB9A
SCHEMBL643837 0.86 BTN3A1 (0.40) LMNANPSR1MAPK1POLBTDP1
SCHEMBL5996997 0.86 BTN3A1 (0.40) LMNANPSR1MAPK1POLBTDP1
SCHEMBL6708631 0.85 LMNA (0.42) LMNAALDH1A1KDM4ESMN1; SMN2KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6465641-B1 METHOD INCLUDES CONTACTING PHOSPHOROUS OXYCHLORIDE WITH A HALOPHENYL MOIETY FOLLOWED BY CONTACTING THE RESULTING HALOPHENYLPHOSPHORODICHLORIDATE WITH A CARBOXY-PROTECTED AMINO ACID AND FINALLY CONTACTING THE RESULTING HALOPHENYLCARBOXY PARKER HUGHES INSTITUTE 2002-10-15 US claimed
US-12121529-B2 Nucleoside phosphoramidate prodrugs GILEAD SCIENCES, INC. (US) 2024-10-22 US disclosed
EP-2203462-B2 NUCLEOSIDE PHOSPHORAMIDATE PRODRUGS GILEAD PHARMASSET LLC (US) 2024-09-25 EP disclosed
US-20240139227-A1 NUCLEOSIDE PHOSPHORAMIDATE PRODRUGS GILEAD PHARMASSET LLC 2024-05-02 US disclosed
EP-2801580-B1 Nucleoside phosphoramidate prodrugs GILEAD SCIENCES INC (US) 2023-09-13 EP disclosed
US-11642361-B2 Nucleoside phosphoramidate prodrugs GILEAD SCIENCES, INC. (US) 2023-05-09 US disclosed
US-20110257122-A1 NUCLEOSIDE PHOSPHORAMIDATE PRODRUGS PHARMASSET, INC. (US) 2011-10-20 US disclosed
US-7964580-B2 Nucleoside phosphoramidate prodrugs PHARMASSET, INC. (US) 2011-06-21 US disclosed
US-7772197-B2 1,3,5-triazines for treatment of viral diseases 1,3,5-Triazines for Treatment of Viral Diseases (US) 2010-08-10 US disclosed
US-7642247-B2 1,3,5-triazines for treatment of viral diseases KORONIS PHARMACEUTICALS, INCORPORATED (US) 2010-01-05 US disclosed
EP-1117669-B1 ANTIVIRAL PURINE DERIVATIVES UNIV CARDIFF (GB) 2003-01-29 EP disclosed
US-6482805-B2 AZT derivatives exhibiting spermicidal and anti-viral activity PARKER HUGHES INSTITUTE 2002-11-19 US disclosed
US-6465641-B1 METHOD INCLUDES CONTACTING PHOSPHOROUS OXYCHLORIDE WITH A HALOPHENYL MOIETY FOLLOWED BY CONTACTING THE RESULTING HALOPHENYLPHOSPHORODICHLORIDATE WITH A CARBOXY-PROTECTED AMINO ACID AND FINALLY CONTACTING THE RESULTING HALOPHENYLCARBOXY PARKER HUGHES INSTITUTE 2002-10-15 US disclosed
US-6407078-B1 THYMINE RING (E.G. AZIDOTHYMIDINE, AZT) THAT HAS 5-HALO, 6-ALKOXY SUBSTITUTION PARKER HUGHES INSTITUTE 2002-06-18 US disclosed
US-20020025922-A1 AZT derivatives exhibiting spermicidal and anti-viral activity UCKUN, FATIH M. 2002-02-28 US disclosed
US-20020022600-A1 AZT DERIVATIVES EXHIBITING SPERMICIDAL AND ANTI-VIRAL ACTIVITY UCKUN, FATIH M. 2002-02-21 US disclosed
US-20010031745-A1 Antiviral purine derivatives UNIVERSITY COLLEGE CARDIFF CONSULTANTS LIMITED (GB) 2001-10-18 US disclosed
EP-1117669-A1 ANTIVIRAL PURINE DERIVATIVES UNIVERSITY COLLEGE CARDIFF CONSULTANTS LTD. (GB) 2001-07-25 EP disclosed
US-6191120-B1 CONTRACEPTIVE; VIRICIDE WAYNE HUGHES INSTITUTE 2001-02-20 US disclosed
WO-2000018775-A1 ANTIVIRAL PURINE DERIVATIVES UNIVERSITY COLLEGE CARDIFF CONSULTANTS LIMITED (GB) 2000-04-06 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 (7 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-20020022600-A1 AZT DERIVATIVES EXHIBITING SPERMICIDAL AND ANTI-VIRAL ACTIVITY TYMP, DUT, UNG LMNA 2473/4885ALDH1A1 919/4885KDM4E 789/4885
US-20240139227-A1 NUCLEOSIDE PHOSPHORAMIDATE PRODRUGS PNP, NUDT1, TYMP LMNA 2469/4885ALDH1A1 1168/4885KDM4E 4570/4885
US-11642361-B2 Nucleoside phosphoramidate prodrugs PNP, NUDT1, TYMP LMNA 2469/4885ALDH1A1 1168/4885KDM4E 4570/4885
US-20020025922-A1 AZT derivatives exhibiting spermicidal and anti-viral activity TYMP, DUT, UNG LMNA 2473/4885ALDH1A1 919/4885KDM4E 789/4885
US-20110257122-A1 NUCLEOSIDE PHOSPHORAMIDATE PRODRUGS PNP, NUDT1, TYMP LMNA 2469/4885ALDH1A1 1168/4885KDM4E 4570/4885
US-20010031745-A1 Antiviral purine derivatives PNP, TYMP, MTAP LMNA 898/4885ALDH1A1 1940/4885KDM4E 1279/4885
US-12121529-B2 Nucleoside phosphoramidate prodrugs PNP, NUDT1, TYMP LMNA 2469/4885ALDH1A1 1168/4885KDM4E 4570/4885

“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.