Carbamic Acid

Carbamic Acid

SCHEMBL1695355

COc1cc(OC)cc(C(=O)C(O)c2ccccc2)c1.NC(=O)O

nearest known ligand 0.55

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.54
CES2 O00748 1/20 0.54
CES1 P23141 1/20 0.54
MEN1 O00255 4/20 0.50
KMT2A Q03164 4/20 0.50
KDM4E B2RXH2 1/20 0.48
ALDH1A1 P00352 1/20 0.48
GPR139 Q6DWJ6 1/20 0.46
PARP1 P09874 1/20 0.45
L3MBTL1 Q9Y468 1/20 0.44
NPC1 O15118 2/20 0.44
RAB9A P51151 2/20 0.44
HTT P42858 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
TACR1 P25103 2/20 0.44
CASP3 P42574 1/20 0.43
SENP8 Q96LD8 1/20 0.43
SENP7 Q9BQF6 1/20 0.43
SENP6 Q9GZR1 1/20 0.43
POLB P06746 1/20 0.43

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
SCHEMBL139043 0.95 LMNA (0.59) LMNACES2CES1MEN1KMT2A
Bicarbonate SCHEMBL2779583 0.94 LMNA (0.58) LMNACES2CES1MEN1KMT2A
Carbamic Acid SCHEMBL1695357 0.88 CES2 (0.54) LMNACES2CES1MEN1KMT2A
SCHEMBL6203480 0.83 CES2 (0.61) LMNACES2CES1MEN1KMT2A
SCHEMBL2337735 0.83 MEN1 (0.43) LMNACES2CES1MEN1KMT2A
SCHEMBL139044 0.83 CES2 (0.59) LMNACES2CES1MEN1KMT2A
Carbamic Acid SCHEMBL4383137 0.82 PARP1 (0.58) LMNACES2CES1GPR139PARP1
SCHEMBL14181968 0.82 CES2 (0.48) CES2CES1MEN1KMT2AKDM4E
Carbamic Acid SCHEMBL23407287 0.82 CA1 (0.50) LMNACES2CES1MEN1KMT2A
Bicarbonate SCHEMBL291493 0.81 CES2 (0.58) LMNACES2CES1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250196456-A1 METHOD FOR THE MANUFACTURING OF AN OPTICAL ELEMENT, OPTICAL ELEMENT THUS OBTAINED ESSILOR INTERNATIONAL (FR) 2025-06-19 US disclosed
US-12263655-B2 Method for the manufacturing of an optical element, optical element thus obtained ESSILOR INTERNATIONAL (FR) 2025-04-01 US disclosed
US-12215100-B2 Anticancer compounds PHARMA MAR, S.A. (ES) 2025-02-04 US disclosed
EP-3898613-B1 ANTICANCER COMPOUNDS PHARMA MAR SA (ES) 2023-08-09 EP disclosed
CN-112789161-B Method for manufacturing an optical element and optical element obtained thereby 依视路国际公司 2022-12-23 CN disclosed
EP-3860838-B1 METHOD FOR THE MANUFACTURING OF AN OPTICAL ELEMENT, OPTICAL ELEMENT THUS OBTAINED ESSILOR INT (FR) 2022-06-22 EP disclosed
US-20220056021-A1 ANTICANCER COMPOUNDS PHARMA MAR, S.A. (ES) 2022-02-24 US disclosed
US-20210379846-A1 METHOD FOR THE MANUFACTURING OF AN OPTICAL ELEMENT, OPTICAL ELEMENT THUS OBTAINED ESSILOR INTERNATIONAL (FR) 2021-12-09 US disclosed
EP-3898613-A1 ANTICANCER COMPOUNDS Pharma Mar S.A. (ES) 2021-10-27 EP disclosed
EP-3860838-A1 METHOD FOR THE MANUFACTURING OF AN OPTICAL ELEMENT, OPTICAL ELEMENT THUS OBTAINED ESSILOR INTERNATIONAL (FR) 2021-08-11 EP disclosed
WO-2014170295-A1 COMPOUNDS POTENTIATING THE ACTIVITY OF ANTIFUNGAL DRUGS FUNDACIÓN MEDINA. CENTRO DE EXCELENCIA EN INVESTIGACIÓN DE MEDICAMENTOS INNOVADORES EN ANDALUCÍA (ES) 2014-10-23 WO disclosed
EP-2792683-A1 Compounds potentiating the activity of antifungal drugs Fundacion MEDINA. Centro de Excelencia en Investigacion de Medicamentos Innovadores en Andalucia (ES) 2014-10-22 EP disclosed
US-8748388-B2 Antitumoral compounds PHARMA MAR, S.A. (ES) 2014-06-10 US disclosed
EP-2576569-A1 SYNTHETIC PROCESS FOR THE MANUFACTURE OF ECTEINASCIDIN COMPOUNDS Pharma Mar S.A. (ES) 2013-04-10 EP disclosed
US-20130066067-A1 Synthetic Process for the Manufacture of Ecteinascidin Compounds PHARMA MAR, S.A. (ES) 2013-03-14 US disclosed
EP-2231695-B1 ANTITUMORAL COMPOUNDS PHARMA MAR SA (ES) 2013-02-13 EP disclosed
WO-2011147828-A1 SYNTHETIC PROCESS FOR THE MANUFACTURE OF ECTEINASCIDIN COMPOUNDS PHARMA MAR, S.A. (ES) 2011-12-01 WO disclosed
US-20110207674-A2 ANTITUMORAL COMPOUNDS PHARMA MAR, S.A. (ES) 2011-08-25 US disclosed
WO-2010149688-A2 ANTITUMORAL COMPOUNDS PHARMA MAR, S.A. (ES) 2010-12-29 WO disclosed
US-20100292163-A1 Antitumoral Compounds PHARMA MAR, S.A. (ES) 2010-11-18 US 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 (5 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-20130066067-A1 Synthetic Process for the Manufacture of Ecteinascidin Compounds SERPINH1, ERLIN2, PTMA LMNA 930/4885CES2 1551/4885CES1 2936/4885
US-20110207674-A2 ANTITUMORAL COMPOUNDS TP53, XPO1, TOP2B LMNA 3075/4885CES2 2449/4885CES1 1265/4885
US-20100292163-A1 Antitumoral Compounds TP53, XPO1, TOP2B LMNA 3075/4885CES2 2449/4885CES1 1265/4885
US-20220056021-A1 ANTICANCER COMPOUNDS TP53, MCL1, MYC LMNA 1756/4885CES2 3537/4885CES1 3249/4885
US-12215100-B2 Anticancer compounds TP53, MCL1, MYC LMNA 1757/4885CES2 3538/4885CES1 3251/4885

“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.