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AB120070

Nociceptin (Orphanin FQ), ORL1 agonist

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(1 Publication)

MW 1809 Da. Achieve your results faster with highly validated, pure and trusted compounds.
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Chemical Structure - Nociceptin (Orphanin FQ), ORL1 agonist (AB120070)
  • Chemical Structure

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Chemical Structure - Nociceptin (Orphanin FQ), ORL1 agonist (AB120070)

2D chemical structure image of ab120070, Nociceptin (Orphanin FQ), ORL1 agonist

Key facts

Form

Solid

form

Molecular weight

1809 Da

Molecular formula

C<sub>7</sub><sub>9</sub>H<sub>1</sub><sub>2</sub><sub>9</sub>N<sub>2</sub><sub>7</sub>O<sub>2</sub><sub>2</sub>

PubChem

56947112

Nature

Synthetic

Solubility

Soluble in water

Biochemical name

(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[2-[[(2S,3R)-2-[[(2S)-2-[[2-[[2-[[(2S)-2-amino-1-hydroxy-3-phenylpropylidene]amino]-1-hydroxyethylidene]amino]-1-hydroxyethylidene]amino]-1-hydroxy-3-phenylpropylidene]amino]-1,3-dihydroxybutylidene]amino]-1-hydroxyethylidene]amino]-1-hydroxypropylidene]amino]-5-carbamimidamido-1-hydroxypentylidene]amino]-1-hydroxyhexylidene]amino]-1,3-dihydroxypropylidene]amino]-1-hydroxypropylidene

Canonical smiles

CC(C)CC(C(=NC(C)C(=NC(CC(=N)O)C(=NC(CCC(=N)O)C(=O)O)O)O)O)N=C(C(CCCCN)N=C(C(CCCNC(=N)N)N=C(C(C)N=C(C(CO)N=C(C(CCCCN)N=C(C(CCCNC(=N)N)N=C(C(C)N=C(CN=C(C(C(C)O)N=C(C(CC1=CC=CC=C1)N=C(CN=C(CN=C(C(CC2=CC=CC=C2)N)O)O)O)O)O)O)O)O)O)O)O)O)O

Isomeric smiles

C[C@H]([C@@H](C(=NCC(=N[C@@H](C)C(=N[C@@H](CCCNC(=N)N)C(=N[C@@H](CCCCN)C(=N[C@@H](CO)C(=N[C@@H](C)C(=N[C@@H](CCCNC(=N)N)C(=N[C@@H](CCCCN)C(=N[C@@H](CC(C)C)C(=N[C@@H](C)C(=N[C@@H](CC(=N)O)C(=N[C@@H](CCC(=N)O)C(=O)O)O)O)O)O)O)O)O)O)O)O)O)O)N=C([C@H](CC1=CC=CC=C1)N=C(CN=C(CN=C([C@H](CC2=CC=CC=C2)N)O)O)O)O)O

InChi

InChI=1S/C79H129N27O22/c1-41(2)33-54(72(122)95-44(5)66(116)103-56(36-59(84)110)73(123)102-53(77(127)128)27-28-58(83)109)104-70(120)49(23-13-15-29-80)100-69(119)52(26-18-32-90-79(87)88)99-65(115)43(4)96-75(125)57(40-107)105-71(121)50(24-14-16-30-81)101-68(118)51(25-17-31-89-78(85)86)98-64(114)42(3)94-61(112)39-93-76(126)63(45(6)108)106-74(124)55(35-47-21-11-8-12-22-47)97-62(113)38-91-60(111)37-92-67(117)48(82)34-46-19-9-7-10-20-46/h7-12,19-22,41-45,48-57,63,107-108H,13-18,23-40,80-82H2,1-6H3,(H2,83,109)(H2,84,110)(H,91,111)(H,92,117)(H,93,126)(H,94,112)(H,95,122)(H,96,125)(H,97,113)(H,98,114)(H,99,115)(H,100,119)(H,101,118)(H,102,123)(H,103,116)(H,104,120)(H,105,121)(H,106,124)(H,127,128)(H4,85,86,89)(H4,87,88,90)/t42-,43-,44-,45+,48-,49-,50-,51-,52-,53-,54-,55-,56-,57-,63-/m0/s1

InChiKey

PULGYDLMFSFVBL-SMFNREODSA-N

IUPAC Name

(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[2-[[(2S,3R)-2-[[(2S)-2-[[2-[[2-[[(2S)-2-amino-1-hydroxy-3-phenylpropylidene]amino]-1-hydroxyethylidene]amino]-1-hydroxyethylidene]amino]-1-hydroxy-3-phenylpropylidene]amino]-1,3-dihydroxybutylidene]amino]-1-hydroxyethylidene]amino]-1-hydroxypropylidene]amino]-5-carbamimidamido-1-hydroxypentylidene]amino]-1-hydroxyhexylidene]amino]-1,3-dihydroxypropylidene]amino]-1-hydroxypropylidene]amino]-5-carbamimidamido-1-hydroxypentylidene]amino]-1-hydroxyhexylidene]amino]-1-hydroxy-4-methylpentylidene]amino]-1-hydroxypropylidene]amino]-1,4-dihydroxy-4-iminobutylidene]amino]-5-hydroxy-5-iminopentanoic acid

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Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Store under desiccating conditions|The product can be stored for up to 12 months
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Product protocols

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Publications (1)

Recent publications for all applications. Explore the full list and refine your search

Science signaling 12: PubMed30914485

2019

Agonist-selective NOP receptor phosphorylation correlates in vitro and in vivo and reveals differential post-activation signaling by chemically diverse agonists.

Applications

Unspecified application

Species

Unspecified reactive species

Anika Mann,Lionel Moulédous,Carine Froment,Patrick R O'Neill,Pooja Dasgupta,Thomas Günther,Gloria Brunori,Brigitte L Kieffer,Lawrence Toll,Michael R Bruchas,Nurulain T Zaveri,Stefan Schulz
View all publications
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